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CAUSES OF BREAST CANCER IN YOUR HOMES & SURROUNDINGS REBECCA B.SINGSON, M.D., FPOGS

Contrary to what many people think, genes account for only 30% of total cancer risk. Most cancers actually result from poor dietary habits, smoking, alcohol consumption, lack of exercise, and exposure to environmental toxins. In fact, so toxic is our environment that the World Alliance for Breastfeeding Action (WABA) and the International POPs (Persistent Organic Pollutants) Elimination Network (IPEN) has declared that if every child born anywhere in this world was tested after birth, we would discover that she or he already has a body burden of toxic chemicals like dioxin, polychlorinated biphenyls (PCB’s), mercury, pthalates, pesticides, flame retardants, bisphenol A and other dangerous substances resulting from transplacental transmission during the prenatal period. These substances are potent hormone disrupters or EED’s (Environmental Endocrine Disrupter meaning they are capable of interfering with the action of hormones like estrogen by increasing or decreases its hormonal effects). This tells us that from the moment of conception, the process of immune system suppression leading to cancer already started from the womb. In fact, by age 6, some kids have already accumulated one half of their total lifetime amount of cancer causing chemicals!! So, it is really no surprise why we are diagnosing breast cancer in women in their 20’s or 30’s with no family history of breast cancer.

FREE RADICALS

Environmental agents cause havoc on our bodies by increasing our load of free radicals. Free radicals are are unstable molecules that seek to steal an electron from another molecule to neutralize it. In the process, it acts like a spitfire from a chimney burning holes on your carpet, only in this case, its your human cells. Everytime you breathe, 3-5% of your oxygen is converted to free radicals as well as when your cells burn food for energy (a process called oxidative metabolism). On top of these, exposure to lead, pesticides, cadmium, ionizing radiation, alcohol and cigarette smoke all serve to increase free radical activity.

To give you an idea of how much damage free radicals can do, imagine that these rebellious molecules strike and fracture every single one of your DNA molecules 10,000 times a day. About 9,900 of these breaks in the DNA strand are restored to normal by DNA repair enzymes. About 100, or 1 percent, escape the enzymes’ notice. This unrepaired damage accumulates over time, setting the stage for atherosclerosis, cancer, and other degenerative diseases. You can see why slowing the damage–by increasing antioxidant protection—is an anti-aging regimen. Meats, poultry, fish, dairy products, and eggs are devoid of protective antioxidants and have instead abundant supplies of free radical-forming fats. They’re also likely to contain residues of pesticides, herbicides, and other free radical-producing toxins

Damaged DNA in the nucleus may provide the wrong genetic code leading to too much protein synthesis and/or cell growth which results in cancer. Malins (1996) determined that women with metastasized breast cancer exhibit twice as much free-radical damage to the breast tissue DNA than do women with localized cancer. The researchers, therefore. concluded that antioxidants, especially vitamin C, may play a crucial role in controlling free radical damage to the DNA in breast tissue and may help prevent metastasis.

TOXIC METALS

Several hundred years ago we did NOT have the burden of toxic metals in our bodies that we now do, and we also did not have such an exposure to free radicals. Free radicals are increased in activity and quantity by bumping into toxic metals in the body. If you remove the toxic metals from the body, you then greatly reduce the activity and the number of free radicals. Here are the two most common toxic metals we are heavily and unknowingly exposed to.

MERCURY – According to FDA toxicologist Mike Bolger, Ph.D., approximately 2,700 to 6,000 tons of mercury are released annually into the atmosphere naturally by degassing from the Earth’s crust and oceans. Another 2,000 to 3,000 tons are released annually into the atmosphere by human activities, primarily from burning household and industrial wastes, and especially from fossil fuels such as coal. Pregnant women and women of childbearing age, who may become pregnant, however, are advised by FDA experts, to limit their consumption of shark and swordfish to no more than once a month. These fish have much higher levels of methyl mercury than other commonly consumed fish. Mercury is also used in fluorescent lights, pesticides, dental fillings & seed coatings. Mercury thermometers can break in a child’s body but this is no cause for alarm since it is poorly absorbed and can be excreted in a the child’s stool but if liquid mercury spills in the house, it vaporizes readily and is easily absorbed through the lungs.

LEAD – heavy metal found in lead crystals, plumbing, PVC, batteries, old paint, tin cans. The Clean Air Act of 1970 in the U.S. and subsequent regulations reduced lead in the atmosphere by 90%. The single most important action was the successful removal of lead from gasoline. The Lead Paint Poisoning Prevention Act of 1971 banned the use of lead in household paint. All houses built before 1960 have leaded paint. Of houses built between 1960-1974 20% have leaded paint. Peeling paint is a serious health hazard. Only experienced professionals should remove it. Household drinking water may contain excessive amounts of lead from the pipes or the lead solder. Ceramic dinnerware may contain lead from the glaze of clay. Therefore used only ceramic dinnerware that has a written statement that it is lead free..

ENVIRONMENTAL POLLUTANTS

Other environmental poisons, from pollutants in the air you breathe to chemicals in the water you drink, generate free radicals as well. While you have less control over them than over your diet, you should still limit your contact with them as much as you can. In fact there are many of these free-radical causing toxins right in your very homes and surroundings increasing your predisposition not only to breast cancer but all other types of cancer as well

DIOXINS – are a family of 75 compounds released into the environment during processes such as bleaching pulp and paper, pesticide production, or when plastic, especially PVC and other chlorinated compounds are manufactured or are burned in older incinerators for example, medical waste like IV bags burned in hospital incinerators can release dioxins which are potent hormone disrupters. More than 95% of all dioxins result from human industrial activity, are emitted into the air then deposited on grass and trees and consumed by cows and other animals or is deposited in lakes and streams and ingested by fish. Since these compounds are insoluble in water, are bound to fatty substances and resilient against degradation, they accumulate in the food chain. Ninety-five % of our exposure to dioxin is through meat, fish and dairy products. In Oct. 1977, dioxin was upgraded to a known human carcinogen, one of the most potent ever tested.

POLYVINYL CHLORIDE (PVC) – or vinyl, is one of the most common of all plastics, used in everything from flooring to children’s toys. The manufacture of PVC generates large quanitities of dioxin and burning PVC plastic can create dioxins, especially in older incinerators. However, new, high tech incineration does not produce dioxins. PVC plastic has been called one of the single most environmentally damaging and least recyclable of all plastics.

POLYCHLORINATED BIPHENYLS (PCB) – class of 209 related oily compounds that don’t burn easily, hence making them excellent as electrical insulator, fire retardants coating wood and plastic, adhesive and lubricant. They enter the environment during manufacture, during spill while transporting, leaks from transformers & burning of waste in incinerators. Production has been banned since 1970 but is still used in other countries. The fish, dairy and poultry we eat are the most consistent sources of PCBs in the food chain. PCBs are found to bind to estrogen receptor sites & at least 24 studies of human populations show a possible link between PCBs and breast cancer.

PTHALATES – class of chemicals used as plasticizers to make plastics more flexible. Used in food packaging materials like cling wrap and food plastics, car parts, toys, blood bags, inks, nail polish, fragrances, antiperspirants, footwear, shower curtains, upholstery, adhesive for medical devices, carpet backing, blister packing, toothbrushes. Soft cheeses, chocolate bars, chips, cakes packaged in paper and cardboard, sausages, contain pthalates, 59 samples from fifteen brands of baby milk, tested by the ministry of Britain in 1996 all revealed pthalates. Pthalates were also found in fruit juices and distilled water possibly leaching from the plastic container. It was also discovered that when some plastic baby feeding bottles were sterilized, pthalates leached into the milk which is why Evenflo brought back tempered glass baby feeding bottles back to the market. Pthalates have been associated with premature breast development, which is linked to early onset breast cancer.

BISPHENOL A – a component of plastic.It can leach into our bodies from food and beverage packaging since they coat metal products like tin cans and bottle tops including baby formula bottles as well as water supply pipes. Used in polycarbonate plastics, dental sealants in our children’s teeth and in composites (the alternative to the mercury in amalgam fillings. Six different laboratories have demonstrated that (BPA) bisphenol A is an estrogen as there are at least two published in vivo studies showing that it is almost as potent as our natural hormones although not as potent as DES. Munoz de Toro (2005) showed that perinatal exposure to BPA in particular, and to estrogens in general, may increase susceptibility to breast cancer.

PESTICIDES – DDT has been linked to breast since women with breast Ca were found to have higher body levels of DDT then women of the same age without cancer. Acc. to WHO, the countries have high exposures to DDT are China, India and Mexico since they still manufactures and use DDT. Much of our pesticide exposure is through our agricultural products laced with pesticides so it is best best to eat only organic produce.
Pesticide poisoning can occur when classrooms or buildings are sprayed for cockroaches, termites, mosquitoes, etc. Many pesticide labels claim people can return to a sprayed area 1-2 hours after application. It is best to keep children away and to thoroughly ventilate area prior to return.
P-chlorobenzene-a registered pesticide which is an active ingredient in moth repellants is found in all types of air fresheners: liquid, spray and solid. This chemical has been demonstrated in tests by the U.S. National Toxicology Program to cause cancers in rats and mice. The pure white cakes commonly placed in urinals and public toilets to freshen the air are made of 100% p-dichlorobenzene.

THE VALUE OF BREASTFEEDING

Maybe one explanation why mothers who breastfeed have a smaller incidence of breast cancer is that breastfeeding considerably lessens the mother’s body burden of toxic chemicals. The chemical levels in mother’s milk become lower during each individual feeding, and are even lower after a three to six month period of breastfeeding, and are also lower for subsequent children.

WHAT SHOULD BE DONE

The public’s health is at stake and cannot to wait for proof that certain chemicals cause breast cancer before the concerned agencies move to prevent the occurrence of such a devastating disease. The following measures should at least be taken:

  • Educate the public about the health effects of radiation and on how to reduce their exposure
  • Tests should be done externsively on all chemicals to check its effect on humans. & phase out chemicals known to cause cancer
  • Corporations should be made liable for hazardous practices .
  • Establish a comprehensive biomonitoring program to measure the presence of chemicals in people and track resultant health outcomes.

SEXUAL ISSUES ON YOUR HONEYMOON

DR REBECCA B. SINGSON, MD, FACS, FPOGS, FPSCPC

I’m a virgin. Will sex hurt? Whats a man supposed to do to prevent from hurting her bride?

A virginal hymen can barely accommodate the pinky finger so getting a man’s organ in can be a bit of a challenge. Whether it will hurt or not will depend upon the man’s skill and patience. There is no substitute for foreplay which begins with sexy whispers, lingering kisses on the ears, neck, mouth and all the erogenous zones lasting a minimum of 20 mins. No attempt at penetration should be done prior to this because women take much longer than men to get fired up for sex. Once well lubricated, only then should the man attempt to insert a finger very slowly to effect gradual dilatation on the hymen. For a virgin, even one finger will hurt, but if done sensually with heightened arousal, it will at least be a pleasurable pain. After one finger is inserted with ease, two fingers can slowly be inserted, then three fingers. Only when this can be done with ease can the man attempt at intercourse.

How can I turn on my groom?

Men are very visual beings so the fact that Victoria’s Secret is a multi-million dollar business is evidence of that. So get yourself irresistibly ravenous with a sexy gear. Aside from learning to set the mood, the woman must get familiar with the man’s anatomy for her to understand how to pleasure her man. The inner thighs of a man, when stroked upwards can trigger the cremasteric reflex, meaning it causes the muscles enveloping the testes to contract, giving an intense ticklish erotic sensation. Kissing and licking the testes and groin areas can give a toe-curling sensation to your man. By the time you get to the penis, understand that it is composed of the head and the shaft. The head part is more sensitive than the shaft so licking or stroking the head can send your man to outer space, especially if you stroke the side near the hole where the urine comes out. But remember that some grooms like women to take the lead yet some men prefer to be in control at all times. So, communicate with your man all the time regarding his preference.

How can I achieve an orgasm?

Unlike men who can achieve an orgasm in two minutes flat, a woman’s sexual anatomy does not allow orgasm to be achieved as easily during intercourse. Upon penetration, the penis is stimulated from tip to base but for the woman, the clitoris gets a piece of the action only during certain positions where the man, or the woman herself, can stimulate the clitoris during contact. There are 4 phases of the human sexual response, namely: the excitement phase, plateau phase, orgasmic phase and resolution. A woman takes normally at least 20 mins. to get warmed up from Excitement Phase to Plateau phase, where her blood supply floods the genitals and nipples causing them to be markedly engorged, and the lower third of the vagina lengthens. The woman has to reach this phase before the Orgasmic Phase can set in. Since the woman’s orgasm is primarily clitoral, orgasm is best achieved when this clitoris is stimulated. Stimulation can be done with the fingers but only if the genitals are well lubricated, otherwise, it can be very unpleasant, or even painful. The tongue provides a much better stimulation because it is not bony and it is a self-lubricating organ.

What most people are not aware of is the presence of the G-spot. This is a 1×1 cm. area corrugated spot on the anterior lower third of the vagina. The best way to feel this is with the woman lying on her back, the man inserts his forefinger, with the palm facing up the ceiling. The G-spot can be felt as a rough spot within an inch or two from the introitus, ridged like the palate of the mouth. Stimulating this for 10 to 15 seconds with a sawing motion, alternating that with clitoral stimulation can give the woman a most powerful orgasm. To help the man along, the woman can contract her butt muscles because the tension can promote an orgasmic response.

Is there any standard position for sex? What position best promotes orgasm for the woman?

The most common position for most couples is the missionary position with the man on top while the woman lies on her back. However, it is not ideal in promoting orgasm for the female because it does not allow much clitoral stimulation. The ideal position to promote orgasm should allow both G-spot stimulation while allowing clitoral stimulation as well. The missionary position can be altered by placing a pillow under the buttocks and bringing the legs up on the man’s shoulders while he is on top of you. This position allows the penis to hit the G-spot while allowing his hand or yours to stimulate the clitoris. The doggie position with the woman kneeling on fours with the man behind, does the same as well as the spoon position where the man is behind the woman in a side-lying position. The woman on top position can cause both G-spot and clitoral stimulation and gives the woman the control in angling herself to achieve maximum stimulation, regulating how fast or slow she wants the thrusts to be as well as adjusting how deep or shallow she wants movements to be.

I’m getting my period during my honeymoon. Is there a way to delay it?

If you anticipate that your period will come during your honeymoon, you may take a birth control pill on the first day of your menses continuously until the day that you are prepared to have your menses.

What’s honeymoon cystitis?

The trauma during intercourse can cause the bacteria to creep up the urethra (the tube leading up to the bladder), causing an infection called cystitis. Since it is very common among virgins having intercourse for the first time, it has been called honeymoon cystitis (but it’s really just a urinary tract infection). To prevent it, urinate immediately after contact to deter the bacteria from creeping up to the urethra. Inform your partner that the bacteria in the rectum is the culprit in 90% of the time so avoid hitting the rectal area during intercourse.

I have a vaginal itch two weeks after I took antibiotics for a cold, can my husband get contaminated from me?

Most likely, what you have is a fungal infection or Candidiasis. This is an opportunistic organism which proliferates itself when your immune system is low or your protective bacteria, the lactobacilli, is destroyed by antibiotics. It is not contagious if the person’s immune system is normal. Thus, unless your husband is immunocompromised, he should not get contaminated.

CARING FOR YOUR WOUND AFTER DELIVERY

Rebecca B. Singson, M.D, FPOGS, FPCPC

After delivery, having a new baby to care for often precedes taking care of ourselves. Sometimes, the medical staff fail to give you the instructions for proper wound care that you neglect to care for your incision whether after a normal deliver or a C-section. The following describes the proper care for your wound post-episiotomy (the incision made on the perineum after a normal delivery) and post Cesarean section.

TYPES OF CLOSURE MATERIALS AND DRESSINGS

There are several ways your doctor will close the wound following a Cesarean section. It may be closed sutures with staples, Steri-strips (small strips of bandages running across the incision line to tape the edges together), and the latest is Super Glue. Staples and Steri-Strips are the least reactive since it only keeps the wound edges together without causing much surrounding tissue reaction. Episiotomies in the perineum are usually closed with sutures, never staples nor Steri-Strips since these are not ideal as the patient continues with her toilet function. There have been reports on the use of cyanoacrylate or Super Glue for wound closure. It works to make wound edges stick by a chemical reaction called polymerization, which produces heat. However, since it uses methyl alcohol, it has a pronounced heating action when it contacts tissue and may even produce burns if the glue contacts a large enough area of tissue. The glue is applied to bridge over the closed edges; it should not be used within the wound (on raw surfaces). The only currently FDA approved adhesives suitable for use as suture alternatives are: (intended for topical skin closure when deep sutures have been placed) Histoacryl Blue (butyl based) (Davis & Geck) and Tissu-Glu (isobutyl based) (Medi-West Pharmaceuticals) are sold for human use.

Immediately after the surgery a form of dressing will be applied over your wound which may be a pressure dressing with thick gauze and some bandage or just a sterile gauze and bandage or a waterproof dressing (brand name Tegaderm or Opsite) that can allow the wound to “breathe” at the same time. In the first 72-96 hours, it is essential to keep the wound dry and clean. Your wound will be inspected to determine if there is any evidence of dehiscence or infection. No dressings are ever applied on perineal wounds.

HOW SHOULD I TAKE CARE OF MY WOUND?

The amount of care your surgical wound will require will be very minimal compared to the amount of care you will be giving your newborn. You may be asked either to keep the wound open or unbandaged. It is best to clean the wound daily with a cotton swab and hydrogen peroxide followed by povidone iodine antiseptic. Make sure you wash your hands thoroughly with soap and water prior to handling your post-op wound. If the wound has some bruising (like a black and blue) around it with minimal swelling, this may be normal from blood that collected during closure. But if there is significant swelling, redness, pain, wound discharge, fever or the wound edges are opening, contact your doctor immediately. That may be a sign of infection and or wound dehiscence.

For an episiotomy wound, one may use a povidone iodine wash (like Betadine vaginal wash) for at least a week post partum then switch to a regular vaginal wash after your doctor has inspected that the wound is on its way to healing.

There have been instances where a blood vessel was not ligated or the ligature loosened up causing an accumulation of blood forming a hematoma in the perineum. If you have any significant pain and swelling especially on one side of the perineum, call the attention of your doctor so your wound may be re-examined.

IS IT NORMAL FOR THE WOUND TO ITCH?
Most of the time, itchiness comes from the dressing applied over the wound to the point where a rash may even occur if the patient has sensitive skin and developed an allergy to her bandage. A mild steroid cream like momethasone can take care of this. Itchiness may also come from the Steri-Strips although I have yet to see anyone develop any allergy to this. Itchiness may also come when the wound starts to heal. The important thing to remember is not to scratch it since you may introduce infection with your nails.

If the episiotomy wound itches, consider a fungal infection in the perineum. This may be common due to the immunocompromised state of the mother, antibiotics given during or after delivery to cure UTI or prophylaxis against infection especially if there had been fecal contamination in the process of delivery.

WHEN CAN I BATHE?
It is a fallacy that postpartum women should not bathe. Some Chinese or Indian elders prohibit their daughters from bathing for a specified number of days to prevent post partum complications. There is no scientific evidence to support this practice. If at all, it may cause more harm than good since the bacteria have a chance to build up.

Different surgeons and obstetricians have different opinions about when to bathe the wound. It is safest to keep the wound covered with a waterproof dressing to prevent it from getting wet while you bathe. A week after discharge from the hospital, you will usually be asked to return to your doctor for wound inspection after which you may bathe if no problem exists with the wound. Soaking in the tub is not allowed until 6 weeks postpartum when the wound is completely healed.

After an episiotomy from a normal delivery you may bathe anytime you can walk normally without feeling dizzy. Otherwise you may lose your balance and slip in the bathroom.

DOES IT HURT TO REMOVE THE CLOSURE MATERIALS?

Most of the time, Cesarean sections and episiotomies are closed with absorbable sutures that need not be removed. Sometimes, there may be a knot on one side of the incision but this may be snipped after a week or just be allowed to fall in time.

Staples, Steri-strips and interrupted sutures may be removed 7-10 days from surgery. There may be some discomfort but not pain associated with the removal of any of these closure materials. Usually the discomfort or pain is from removing the sticky bandage. One can use a cotton ball with alcohol and apply it underneath the dressing to facilitate separating the dressing from the skin.

Although caring for your post-partum wound is an important step to insure a good outcome, remember that your immune system is what will heal your wound. How you eat and what supplements you take can do much to help you strengthen your immune system at a time when you have very little sleep since you are caring for your newborn. A good wound outcome depends on how you have been caring for your body throughout your pregnancy. Bear in mind that a healthy body will have a good wound outcome with minimal complications.

SUMMER SPORTS AND PREGNANCY

Rebecca B. Singson, MD, FPOGS, FPCPC

With summer clearly manifesting its heat coupled with the end of the school year, families have the time to plan for outings and vacations. For pregnant women, especially for first-time moms, knowing what your limits are in terms of activity can surely keep injury away from you and your baby.

CAN I SWIM?

Yes, certainly. This is one of best exercises for pregnant woman. It mobilizes many different muscles yet there is little strain for the woman to bear the load of that growing tummy since the water supports and partially unburdens her of that weight.  Diving or jumping into the water are best avoided, however, especially in the third trimester of pregnancy. The problem with pools is that the water is chlorinated for antiseptic reasons, i.e. to kill the harmful bacteria that may accumulate in the water. That’s good. But the bad side is the chlorine can also kill the bacteria in the vulvar area, upsetting the bacterial flora, thus promoting fungal infections. So if you get a vaginal itch a few days to a few weeks after swimming, you know what caused it and what it might possibly be.

In the beach, avoid jellyfish stings with a locally available anti-jellyfish lotion by Godiva. Remember to be generous with sun block to prevent free radical formation on the skin (the higher the number, the longer the protection. Look for SPF60) that can induce skin cancer as well as to wear sunglasses to avoid free radical formation in the eyes that can cause cataracts in the future. Prevent dehydration and overheating by taking lots of fluids (coconut juice is great for replenishing electrolytes − much better than plain water).

Avoid water sports that create internal body pressure changes, such as scuba diving. Water skiing and beach volleyball are best avoided but jet skiing may be engaged in if it is something you have been doing even prior to pregnancy, not if you are learning it for the first time.

WHAT ABOUT OTHER SPORTS?

One rule of thumb when it comes to activities and pregnancy is that you can usually engage in it if it was something you have been accustomed to doing prior to pregnancy. However, activities where you run the risk of falling are best to be avoided, since the force of an impact may cause the placenta to separate from the uterus, known as abruption placenta. This is a very serious condition, which will cut off the oxygen supply of the baby, causing fetal death or a dangerous loss of blood from the mother. Therefore, rock climbing, skydiving and horseback riding are definitely to be avoided. Tennis is generally safe during pregnancy if you are not learning it for the first time. A woman should be aware that her sense of balance may change.  Golf and bowling are good recreational sports but don’t consistently pump up cardiovascular function so they don’t really strengthen the heart and lungs. What a pregnant woman needs to remember, however, is that during pregnancy, the hormone, relaxin, causes all the joints to loosen. Furthermore, with a growing abdomen, her axis of gravity changes such she will need to lean back to adjust to her balance. Body-building and strength training can make muscles stronger as well as help prevent the muscle aches and pains that are commonly experienced in pregnancy. This is best done with a professional trainer to avoid muscle and joint injuries.

POINTS TO REMEMBER

  1. Vigorous exercises can raise a woman’s temperature to more than 1 ½ to 2 degrees F. This can be dangerous since blood is shunted from the uterus to the skin to regulate temperature back to normal.
  2. No swimming in hot springs or hot tubs. Avoid saunas and steam rooms.
  3. Wear stretchable or loose clothes that don’t strangle any part of the body with movement. Natural fabrics like cotton let the body breathe vs polyester fabrics that don’t absorb sweat.
  4. Use anti-slip footwear especially in wet areas. Use well-fitting, well-cushioned sneakers that will protect the loosened joints and ligaments of the body to minimize injuries.
  5. Never train to the point of exhaustion. Once the body sugar runs low, the body will break down fat for energy supply. The by-product of this fat metabolism is ketone formation which can cross the placenta and is not safe for the fetus.
  6. Whenever pain, cramping, dizziness, nausea and headache ensue, these are body signals that should never be ignored and should be signs that it is time to stop and rest.
  7. Gradually reduce the level of exercise in the third trimester. Walking is the best exercise at this stage of pregnancy, which does the least harm.

It is possible to enjoy the summer and some of the fun activities with friends and family if you know what your limits are as a pregnant woman. As in many other things during pregnancy, it is better to be safe than sorry.

All About Stretch Marks

Rebecca B. Singson, MD, FPOGS, FPSCPC

WHAT ARE STRETCH MARKS?

Stretch marks, also known as stria atrophica or striae distensae, is a common skin condition that has no serious medical consequences yet, can cause a major cosmetic concern to people to have it. It may appear in the shoulders of body builders, in the buttocks of adolescents undergoing their growth spurt, and in the arms, breasts, buttocks and thigh of individuals who are overweight. Seventy percent (70%) of adolescent females, and 40% of adolescent males, especially those who participate in sports, have stretch marks. If it occurs during pregnancy, it is called striae gravidarum. It is found in 90% of pregnant white women but is less common among Asian and black women. (2) Striae generally develop late in the 2nd trimester and the areas most frequently affected are the breasts and abdomen.

WHAT CAUSES STRETCH MARKS?

The cause of stretch marks is still unclear, although genetic predisposition, hormones and weight gain during pregnancy each appear to have a role in the etiology. Prolonged use of oral or topical corticosteroids or Cushing syndrome (increased adrenal cortical activity) also causes striae. They represent linear dermal scars accompanied by atrophy of the epidermal layer of the skin.

The skin has three different layers. The top layer is known as the epidermis, the middle, elastic layer is called the dermis, and the deepest layer is called the subcutaneous layer. Stretch marks actually occur in the elastic dermis layer.

These are caused by tearing in the skin and its underlying connective tissue as a result of direct trauma or stretching due to the enlargement of muscle or adipose (fat) tissue. As underlying tissue enlarges due to sudden and drastic weight gain, the dermis is stretched too far too quickly and its collagen fibers break, thus, leaving some microscopic bleeding and inflammation that become the dreaded stretch marks. If you look under the microscope, it will reveal that elastic fibers are absent in the area of the defect and are curled and clumped at the sides. At first, stretch marks appear slightly raised and pink, reddish brown, or dark brown lines that then turn purple or violet. Over time, these lines will fade in color and become almost silvery in comparison to your normal skin tone.

HOW CAN I PREVENT STRETCH MARKS?

A healthy diet for prevention of stretch marks is one that incorporates all the essential amino acids and essential fatty acids, enough Vitamins C and E as well as the minerals zinc and silica have been known to help form collagen and aid in tissue regeneration.

The market abounds with products for stretch mark  prevention. One such product is The Stretch Mark PreventionTM cream which contains 100% natural ingredients such as squalene oil, vitamin E, vitamin A, vitamin D3 as well as aloe vera and grapefruit seed extracts. Together they are designed to blend to increase the elasticity of the skin and stimulate the production and regeneration of new skin cells. Shea butter and olive oil have been age old preventive treatments for stretch marks. PhytoelastinTM, from France, is one of the few products with scientific studies to back up its claim of preventing stretch marks.  Cochrane analysis shows that applying products on the skin does work to prevent stretch marks, although it is not clear whether it is the product that causes the prevention or the act of massaging the skin, thus increasing the circulation that does the trick.

IF I ALREADY HAVE STRETCH MARKS, HOW CAN I GET RID OF IT?

PhytolastinTM has 2 product lines for prevention of stretch marks during pregnancy and another product after delivery to help fade stretch marks. Its proprietary formula changes the composition of your skin deep, deep in the dermal level where new skin cells are made.

StriPeptin™ , is another product that claims to stimulate cell production around the damaged areas, giving a noticeable improvement in your stretch marks. They claim that 93% of users in their clinical study could see a clear, measurable difference in the appearance of their marks after just 8 weeks.

Retinoids — Topical retinoids have been shown to be beneficial in remodeling hypertrophic scars and in improving the clinical appearance, including improvement of the surface texture, fine and coarse wrinkling, skin color, and laxity, of photoaged skin after 3-6 months of therapy.Drug Name

Tretinoin (Avita, Retin-A) — Trans-retinoic acid is a derivative of vitamin A (retinol), effectively used to treat acne vulgaris and other disorders of keratinization for the past 3 decades. It exhibits a certain degree of vitamin A growth-promoting activity and in epithelial cell promotes collagen synthesis.. Topical application significantly improves clinical appearance of early, active stretch marks. Patients are instructed to gradually increase amount of tretinoin until mild erythema and exfoliation develops; may also apply a bland emollient if excessive irritation develops.  It is recommended to apply 0.05% or 0.1% cream on affected areas once or twice a day

Bio Oil is a recent natural product, available in local drugstores made of Vitamin A, Vitamin E, Calendula Oil, Lavender Oil, Rosemary Oil and Chamomile Oil. It has been found to effectively reduce stretch marks (quite safe to use in pregnancy because of the natural oils), prevent the appearance of stretch marks, as well as improve the appearance of scars because it helps enhances the production of collagen.

Early red stretch marks can be improved with the pulsed dye laser. However, older stretch marks show both whitening of the skin (hypopigmentation) and thinning of the skin (atrophy). Although there is no treatment for the atrophy, there are UV lasers developed for the treatment of the white skin associated with stretch marks. The laser emits short powerful pulses of ultraviolet light that stimulate the pigment-producing cells of the skin (melanocytes) to make melanin. The melanin results in a darkening of the white stretch marks and brings the stretch mark skin closer to the natural color of the surrounding skin. By decreasing the whiteness of the stretch marks and making the skin color more normal, the stretch marks become much less noticeable. Treatments are effective for all skin types and ages. Partial pigmentation of stretch marks starts after 3-6 treatments. Treatments are usually delivered twice a week for 4-6 weeks with an 80 percent response rate which varies among patients.

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 INTRODUCTION  Section 2 of 10      

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Background: Striae distensae, a common skin condition, do not cause any significant medical problem; however, striae can be of significant distress to those affected. They represent linear dermal scars accompanied by epidermal atrophy.

Pathophysiology: Striae distensae affect skin that is subjected to continuous and progressive stretching; increased stress is placed on the connective tissue due to increased size of the various parts of the body. It occurs on the abdomen and the breasts of pregnant women, on the shoulders of body builders, in adolescents undergoing their growth spurt, and in individuals who are overweight.

Skin distension apparently leads to excessive mast cell degranulation with subsequent damage of collagen and elastin. Prolonged use of oral or topical corticosteroids or Cushing syndrome (increased adrenal cortical activity) leads to the development of striae. Genetic factors could certainly play a role, although this is not fully understood.

Frequency:

In the US: Approximately 90% of pregnant women, 70% of adolescent females, and 40% of adolescent males (many of whom participate in sports) have stretch marks.

Internationally: International figures may reasonably mirror the numbers in the United States.

Mortality/Morbidity: Striae distensae are usually a cosmetic problem; however, if extensive, they may tear and ulcerate when an accident or excessive stretching occurs.

Race: Stretch marks affect persons of all races.

Sex: Striae affect women more commonly than men.

Age: Stretch marks affect adolescents, pregnant women, and patients with excessive adrenal cortical activity.

 CLINICAL  Section 3 of 10      

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Physical: Early striae present as flattened, thinned skin with a pink hue that may occasionally be pruritic. Gradually, they enlarge in length and width and become reddish purple in appearance (striae rubra). The surface of striae may be finely wrinkled. Mature striae are white, depressed, irregularly shaped bands, with their long axis parallel to the lines of skin tension. They are generally several centimeters long and 1-10 mm wide. Gradually, some striae may fade and become inconspicuous. The natural evolution of stretch marks is similar to that of scar formation or a healing wound.

In pregnancy, striae usually affect the abdomen and the breasts.

The most common sites for striae on adolescents are the outer aspects of the thighs and the lumbosacral region in boys and the thighs, the buttocks, and the breasts in girls. Considerable variation occurs, and other sites, including the outer aspects of the upper arms, are occasionally affected.

Striae induced by prolonged systemic steroid use are usually larger and wider than other phenotypes of striae, and they involve widespread areas, occasionally including the face.

Striae secondary to topical steroid use are usually related to enhanced potency of the steroids when using occlusive plastic wraps. They usually affect the flexures and may become less visible if the offending treatment is withheld early enough.

Causes:

The factors that lead to the development of striae are poorly understood. No general consensus exists as to what causes striae. One suggestion is that they develop as a result of stress rupture of the connective tissue framework. It has also been suggested that they develop more easily in skin that has a high proportion of rigid cross-linked collagen, as occurs in early adult life. This is evident in striae due to pregnancy, lactation, weight lifting, and other stressful activities. Increased adrenal cortical activity has been implicated in the formation of striae, as in the case of Cushing syndrome. Additionally, the cellular and extracellular matrix alterations that mediate the clinical phenotype of stretch marks remain poorly understood.

 DIFFERENTIALS  Section 4 of 10      

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Other Problems to be Considered:

Although the diagnosis of striae is usually straightforward, the rare possibility of Cushing syndrome must be entertained. In the latter, striae are characterized by their inordinate breadth, depth, and intense color.

In linear focal elastosis (elastotic striae), asymptomatic, yellow linear bands arrange themselves horizontally over the lower back. These lesions may resemble striae distensae, but they are palpable rather than depressed and yellow rather than purplish or white.

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WORKUP  Section 5 of 10      

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Histologic Findings: In the early stages, inflammatory changes may predominate; edema is present in the dermis along with perivascular lymphocyte cuffing.

In the later stages, the epidermis becomes thin and flattened with loss of the rete ridges. The dermis has thin, densely packed collagen bundles arranged in a parallel array horizontal to the epidermis at the level of the papillary dermis. Elastic stains show breakage and retraction of the elastic fibers in the reticular dermis. The broken elastic fibers curl at the sides of the striae to form a distinctive pattern.

Scanning electron microscopy shows extensive tangles of fine, curled elastic fibers with a random arrangement. This arrangement is in contrast to normal skin, which has thick, elastic fibers with a regular distribution. When viewed by transmission electron microscopy, the ultrastructure of elastic and collagen fibers in striae is similar to that of healthy skin.

 TREATMENT  Section 6 of 10      

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Medical Care:

Adolescents with striae can expect some improvement in their striae with time.

Topical application of tretinoin can significantly improve the clinical appearance of early striae distensae.

Surgical Care: The authors have had good success using low concentrations (15-20%) of trichloroacetic acid (TCA) and performing repetitive papillary dermis-level chemexfoliation. The peels can be repeated at monthly intervals. Significant improvement in regard to skin texture, firmness, and color can be achieved.

Treatment with the 585-nm flashlamp pulsed dye laser at low energy densities was shown to improve the appearance of striae. Multiple treatments at 4- to 6-week intervals are usually required.

Certainly, both modalities (pulsed dye laser and TCA peels) can be sequentially performed for optimal results.

At lower fluences (2-4 J/cm2), The 585-nm flashlamp pulse dye laser (FLPDL) has been purported to increase the amount of collagen in the extracellular matrix. The 585-nm FLPDL has a moderate beneficial effect in reducing the degree of erythema in striae rubra but has no apparent benefit in striae alba. Because of the potential for adverse effects, FLPDL treatments should be performed with extreme caution or even not at all in darker-skinned patients (phototypes V and VI).

Intense pulse light, a noncoherent, nonlaser filtered flashlamp that emits a broadband visible light, has been reported to yield clinical and microscopical improvement in striae distensae. It seems to be a promising treatment modality with minimal adverse effects and little to no down time.

Lasers and light sources emitting UV-B irradiation have been shown to repigment striae distensae (striae alba). The improvement is due to an increase in melanin pigment, hypertrophy of melanocytes, and an increase in the number of melanocytes.

MEDICATION  Section 7 of 10      

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Drugs of choice should have the ability to improve the skin texture and color, to remodel the collagen in the dermis, and to promote elastin synthesis.

Drug Category: Retinoids — Topical retinoids have been shown to be beneficial in remodeling hypertrophic scars and in improving the clinical appearance, including improvement of the surface texture, fine and coarse wrinkling, skin color, and laxity, of photoaged skin after 3-6 months of therapy.Drug Name

Tretinoin (Avita, Retin-A) — Trans-retinoic acid is a derivative of vitamin A (retinol), effectively used to treat acne vulgaris and other disorders of keratinization for the past 3 decades. Exhibits a certain degree of vitamin A growth-promoting activity; however, it is not stored in the body as retinol and its esters. Rather, it is metabolized rapidly and mostly excreted in bile. When administered topically, a minute amount passes through dermis but has not been detected systemically.

In epithelial cells, affects differentiation, neoplastic transformation, tumor promotion, collagen synthesis, wound healing, stimulation and modulation of immune response, inflammation, cell membranes, and many other processes.

0.05% strength has been shown to improve hypertrophic scars. Postulated that this is due to effect on fibroblasts (ie, decreased fibroblast proliferation and decreased fibroblast collagen synthesis). Effect on fibroblasts is mediated through specific binding receptor proteins. Topical application significantly improves clinical appearance of early, active stretch marks. Processes responsible for clinical improvement remain unknown.

Patients are instructed to gradually increase amount of tretinoin until mild erythema and exfoliation develops; may also apply a bland emollient if excessive irritation develops.

Adult Dose Apply 0.05% or 0.1% cream on affected areas qd/bid

Pediatric Dose Apply as in adults

Contraindications Documented hypersensitivity

Interactions Concomitant topical medication, medicated or abrasive soaps, and cleansers, soaps, and cosmetics have strong drying effects; caution with products high in alcohol, astringents, spices or lime, and preparations containing sulfur, resorcinol, or salicylic acid because tretinoin toxicity may increase

Pregnancy C – Safety for use during pregnancy has not been established.  

Precautions Discontinue if reaction suggesting sensitivity or chemical irritation occurs; minimize exposure to sunlight, including sunlamps, during use, and advise patients with sunburn not to use product until fully recovered because of heightened susceptibility to sunlight; wearing protective clothing and applying sunscreen products over treated areas is recommended; weather extremes (eg, wind, cold) may irritate patients; degree of local irritation warrants either less frequent applications or treatment to be discontinued (temporarily or altogether)

 FOLLOW-UP  

  • Arnold HL, Odom RB, James WD: Abnormalities of dermal connective tissue. In: Odom RB, James WD, Berger TG, eds. Andrew’s Diseases of the Skin Clinical Dermatology. 9th ed. Philadelphia, Pa: WB Saunders; 2000: 645-6.
  • Burton Jl, Lovell CR: Disorders of connective tissue. In: Champion RH, Wilkinson DS, Ebling FJG, et al, eds. Textbook of Dermatology. 6th ed. London; Blackwell Science; 1998: 2008-9.
  • Dover JS: Sports dermatology. In: Fitzpatrick TB, Eisen AZ, Wolff K, Freedberg IM, eds. Dermatology in General Medicine. 4th ed. New York, NY: McGraw-Hill; 1993: 1618-19.
  • Fox JL: Pulse dye laser eliminates stretch marks. Cosmetic Dermatology 1997; 10: 51-2.
  • Goldberg DJ, Marmur ES, Schmults C, et al: Histologic and ultrastructural analysis of ultraviolet B laser and light source treatment of leukoderma in striae distensae. Dermatolog Surg 2005; 31(4): 385-7[Medline].
  • Goldfarb MT, Ellis CN, Weiss JS, Voorhees JJ: Topical tretinoin therapy: its use in photoaged skin. J Am Acad Dermatol 1989 Sep; 21(3 Pt 2): 645-50[Medline].
  • Hernandez-Perez E, Colombo-Charrier E, Valencia-Ibiett E: Intense pulsed light in the treatment of striae distensae. Dermatol Surg 2002; 28(12): 1124-30[Medline][Full Text].
  • Jimenez GP, Flores F, Berman B, Gunja-Smith Z: Treatment of striae rubra with the 585-nm pulsed-dye laser. Dermatol Surg 2003; 29(4): 362-5[Medline].
  • Kang S, Kim KJ, Griffiths CE, et al: Topical tretinoin (retinoic acid) improves early stretch marks. Arch Dermatol 1996 May; 132(5): 519-26[Medline].
  • Kang S, Kim KJ, Griffiths CE, et al: Topical tretinoin (retinoic acid) improves early stretch marks. Arch Dermatol 1996 May; 132(5): 519-26[Medline].
  • Kligman A: Topical tretinoin: indications, safety, and effectiveness. Cutis 1987 Jun; 39(6): 486-8[Medline].
  • McDaniel DH, Ash K, Zukowski M: Treatment of stretch marks with the 585-nm flashlamp-pumped pulsed dye laser. Dermatol Surg 1996 Apr; 22(4): 332-7[Medline].
  • McDaniel DH: Laser therapy of stretch marks. Dermatol Clin 2002; 20: 67-76[Medline].
  • Medical Economics Staff: Physician’s Desk Reference. 53rd ed. Medical Economics Company; 1999: 2177.
  • Obagi ZE, Obagi S, Alaiti S, Stevens MB: TCA-based blue peel: a standardized procedure with depth control. Dermatol Surg 1999 Oct; 25(10): 773-80[Medline].

ADVICE TO PREGNANT WOMEN: HOW TO AVOID OVEREATING DURING THE HOLIDAYS

By Rebecca B. Singson, MD, FPOGS

Whenever it’s holiday time, it becomes challenging for people to maintain their weights because of the frequent social engagements and office parties loaded with mouth-watering, irresistible goodies. It becomes particularly challenging for the pregnant woman who has an increased appetite and feels she “is eating for two” but is already overweight. If you are slim and non-pregnant, gaining extra weight and eating high calorie but low nutritional food may not be such a great issue. But to the infanticipating woman, there may be more serious consequences if she is not meticulous in watching what she eats so here’s the why and how of being more prudent with your palate during party time.

WHY YOU SHOULD NOT GAIN TOO MUCH WEIGHT

Too many calories and extra pounds can put you at a higher risk for pregnancy complications such as hypertension or diabetes, and may make labor and delivery more difficult. Although you do need extra calories during pregnancy, particularly during the last trimester, you also need lots of extra nutrients, so those extra calories need to be chosen wisely. A woman who is not pregnant needs between 1,800 and 2,200 calories per day. When you are pregnant, contrary to popular belief, you only need to increase your calories by about 300 per day so keep in mind that its quality not quantity is what matters. Remember that if you gain way beyond the prescribed weight, your chances of having a large baby also increases, which in turn may also increase your chances of ending up with a Cesarean section.

Besides all that, the latest, and by far the most disturbing finding by researchers at Lombardi Cancer Center in Washington, DC, and in Finland is that women who gain more than 50 pounds during pregnancy, and did not losing the excess weight after pregnancy, can triple their risk of developing breast cancer after menopause. A lesser pregnancy weight gain of 40 pounds can still increase breast cancer risk by 40%. Knowing that should stimulate you to be more watchful of the weighing scale.

Researchers have shown that pregnancy weight gain has been linked to increased estrogen levels, which in turn is believed to increase breast cancer risk  in a similar way that postpartum obesity does too. Women who gained within the normal limit of 25-35 lbs. during pregnancy were not associated with increased breast cancer risk.

If despite eating moderately, you are gaining more than 2 lbs./wk., you must alert your obstetrician since any rapid weight gain, especially if associated with marked fluid retention and an increase in blood pressure and possibly protein in the urine, can be a marker for the onset of preeclalmpsia. This is a disorder that can be harmful, if not fatal to you and your baby.  

HOW MUCH IS TOO MUCH?

If you are of average weight, it is recommended that you gain is about 25 pounds during pregnancy. Only two to four pounds of that goes on during the first trimester. By 20 weeks, you should have gained 7-10 lbs. and the remaining weigt is added at about a rate of half a pound to one pound per week after that. Some women even drop their weight during the first trimester due to nausea and vomiting but usually recover the weight loss in the course of pregnancy. Underweight moms can afford to gain more weight, at least 28 to 40 pounds, so they don’t end up with a low birth weight baby. But if you’re already carrying an extra baggage of fat by the time you get pregnant, its best that you limit your weight gain to 15-20 lbs.

If you want to know where all that weight goes, here’s how the weight gain is ideally distributed:

  • Baby:   7 pounds
  • Placenta:   1 pound
  • Amniotic fluid:   2 pounds
  • Blood volume:   4 pounds
  • Body fluids:   3 pounds
  • Uterus:   2 pounds
  • Breasts:   1 pound
  • Fat & protein storage:   7 pounds

 

WHAT YOU CAN DO

So you can’t say no to these social obligations. At the same time, you’d hate to miss out on the fun. So here are tips to help you keep the scale from tipping over.

  • PRIORITIZE YOUR REQUIREMENTS. Make sure you meet your daily requirements first before you allow yourself the treats. Get your fill of the salads and protein sources while filling your healthy carbohydrate requirements. Ear your fruit first before you hover over the dessert table. Hopefully, that would have killed your craving for the pastry department.
  • AVOID STARVATION. It is truly difficult to control your appetite if you arrive ravenous during a party. You are bound to eat everything in sight! So before you go to the party, have a nutritious snack like a granola or muesli bar, veggie sticks with yoghurt-garlic dip or some dried fruits and nuts so you won’t be obsessing over the buffet table.
  • DRINK BEFORE YOU LEAP.  If you have the urge to splurge, gulp down a glass of water, fruit juice or some soup (preferable clear than creamed). That will instantly appease your grumbling insides and allow you to be more sane and prudent in your choice of food.
  • CHEAT SENSIBLY. If you must absolutely give in to your sweet tooth, at least make the wiser, more nutritious choice, lower calorie choice. An oatmeal or ginger cookie is better than an empty sponge cake or a fatty cheese cake.
  • IF YOU MUST INDULGE, EAT ONLY A PORTION OF IT.  If you cant resist the cheesecake, instead of gobbling up the whole slice, eat only half or a few bites of it. Remember, it doesn’t matter whether you have had fifty bites or only two. In the end, your mouth is empty. But the fifty bites will take your weight farther down the scale.
  • BURN WHAT YOU EAT.  Just because you are pregnant doesn’t mean you can’t exercise. As a rule, you can still continue your exercises, dance or low impact sports (swimming, golf, tennis doubles). Remember that brisk walking for 20 mins., will raise your metabolism the rest of the day and cause you to burn calories faster than if you did not exercise at all.
  • DON’T BE A STRESS CHOMPER. Holidays can be stressful times especially when you have to socialize and beat you office deadlines at the same time. So resist the impulse to munch away your stress. Be prepared with your arsenal of anxiety busters like yoga, meditation, massage (caution: masseuse must be trained on pregnant women or premature labor may be induced), instead of taking it out on food.

 

Remember that staying within your prescribed weight will insure a more favorable outcome for your pregnancy as well as prevent your risk for breast cancer. That’s really worth dieting for.

MICRONUTRIENT SUPPLEMENTATION IN PREGNANCY

Rebecca Singson, M.D., FPOGS

Pregnancy is in the only time in the life of a woman when another human being becomes a parasite to her, depending on her body to provide the nutrients the fetus needs in order to grow. It is thus a critical time to be equipped with the necessary micronutrients to prevent damage to the growing fetus as well as to the mother herself. Nature protects the fetus so much that if the baby needs a nutrient that the mother does not have enough of for herself and her baby, the nutrient will be preferentially directed to the baby even to the detriment of the mother.

In this generation when we no longer plant our food the way our forefathers did, the nutrition we get from eating fastfood, bottled, canned, frozen food have become devoid of the nutrients we need to keep our bodies healthy, much less to support a healthy pregnancy. We need to insure ingesting at least the following nutrients to begin working towards an uneventful pregnancy.

FOLIC ACID. Folic acid can be found in foods such as spinach, parsley, broccoli, lettuce, lima beans, turnip greens, asparagus and beef liver. Folic acid supplementation is best taken even before planning your pregnancy since there is strong evidence that folic acid can reduce certain birth defects of the brain and spinal cord by more than 70 percent. These birth defects are called neural tube defects (NTDs). NTDs happen when the spinal cord fails to close properly.The most common neural tube defect is spina bifida which occurs when part of the baby’s spinal cord remains outside the body. The baby may have paralyzed legs and, later, may develop bladder and bowel control problems. The most serious neural tube defect is anencephaly when baby is born without part of its skull and brain, and eventually dies. For all childbearing ages, the Center for Disease Control in the U.S. recommends that all women of childbearing age take at least 400mg of folic acid daily but for all pregnant women, 1mg/day is recommended. Women with a history a child with neural tube defect should take 4 mg of  folic acid 1 month prior to conception and and all throughout the first trimester.1

IRON. According to the Cochrane review, rron supplementation appears to prevent low haemoglobin at birth or at six weeks post-partum.2 The availability or iron for our bodies to use depends on the food source. Heme iron, which is found only in meat, poultry, and fish, is two to three times more absorbable than non-heme iron, which is found in plant-based foods and iron-fortified foods 3.4. The bioavailability of non-heme iron is strongly affected by the kind of other foods ingested at the same meal. Enhancers of iron absorption are heme iron (in meat, poultry, and fish) and vitamin C; inhibitors of iron absorption include polyphenols (in certain vegetables), tannins (in tea), phytates (in bran), and calcium (in dairy products)5.6 . Vegetarian diets, by definition, are low in heme iron but can certainly be increased by careful planning of meals. The CDC recommends taking or low dose 30 mg/day) supplements of iron at the first prenatal visit. In the presence of anemia, treatment involves prescribing an oral dose of 60-120 mg/day of iron.7.

IODINE. This is essential for normal fetal thyroid function. If the mother lacks iodine, the baby may develop cretinsm (congenital hypothyroidism) of which mental retardation is a component. Cretins have abnormal looking faces with the tongue sticking out. Acc. to the Cochrane Review, iodine deficiency is the leading preventable cause of intellectual impairment in the world. Supplementation during pregnancy especially in areas with high incidence of cretinism results in reduction of this problem with no adverse side effects.8

The use of iodized salt is one way to prevent iodine deficiency. Salmon, tuna and seaweeds are excellent leading sources of iodine from food.

If using seaweeds as an iodine source it is best to use seaweeds that have been found to have a fairly consistent iodine content, such as kelp (kombu) or hijiki. It may be dangerous to consume more than 100g/year (by dried weight) of most seaweeds carries a significant risk of thyroid disorder due to iodine intakes in excess of 1000 micrograms per day.

Nori (the seaweed used to wrap sushis with) is low in iodine and several sheets a day can be eaten without any concern about excess iodine. Frequent addition of small amounts of powdered or crumbled seaweed to stews or curries while cooking, or to other foods as a condiment, is an excellent way to provide adequate iodine (in the absence of other supplementation) . 100g of dried hijiki or 15g of dried kombu or kelp in a convenient container in the kitchen provides one year’s supply for one person.

MAGNESIUM. Magnesium supplementation during pregnancy has been associated with fewer pre-term births and less intrauterine growth retardation. 9.10,11 Magnesium deficiency is associated with pre-eclampsia, and pre-term delivery and possibly with low birth weight.12 ,  coagulation defects 13, premature delivery14,15, intrauterine growth retardation 9.15,and muscle cramping16 Diets high in magnesium density would contain whole grains, lean meats, low amounts of fats and sugars, abundant fruits and vegetables, and low-fat milk. Diets low in magnesium density would contain refined cereal grains, fatty meats, high amounts of fats and sugars, few fruits and vegetables and sugar-containing soft drinks.

DHA. In the latest researches it has been found that supplementing pregnant mothers with fish oil may benefit brain and retinal development in their offspring particularly if born prematurely. Supplementing from mid-pregnancy to the 34th week was found to be perfectly safe and more importantly, may reduce the incidence of preeclampsia (pregnancy-related high blood pressure).17 It was found that breastmilk contains DHA whereas formula milk did not. Researchers at the University of Milan report that infants whose formula contains long- chain polyunsaturated fatty acids [especially Docosahexaenoic acid (DHA)] have better brain development than children who do not receive DHA in their formula. The observation supports earlier findings that there is a direct correlation between the DHA concentration in the red blood cells of infants and their visual acuity. The researchers recommend that infants who are not breastfed be fed on a DHA- enriched formula. Nothing is as complete as breast milk since it is already complete with the fatty acids necessary for good brain development.

VITAMIN D:

Vitamin D is produced by the skin and eyes from exposure to sunlight and can also be consumed from foods such as fish-liver oils, fatty fish, mushrooms, egg yolks, and liver. Thus nutrient has multiple functions in the body like helping maintain bone integrity and calcium homeostasis. During pregnancy, vitamin D deficiency or insufficiency may develop. Vitamin D supplementation during pregnancy has been suggested to safely improve pregnancy and infant outcomes. 

Research shows that the Vitamin D supplementation during pregnancy improves the women’s vitamin D levels, as measured by 25-hydroxyvitamin D concentrations at term and may reduce the risk of delivering a baby prematurely (less than 37 weeks of gestation), result in a lower risk of high blood pressure in women and reduce the risk of a low birthweight baby (less than 2500 g).19

MICRONUTRIENT INTERACTIONS.

There are some micronutrients that alter the absorption of others. For example, calcium can block the absorption of iron. Vitamin A may also contribute to anemia by interfering with iron although studies have shown that when given together, there is greater reduction in anemia. Iron supplements can also interfere with the absorption of zinc. On the other hand, vitamin C can increase the absorption of and zinc. Zinc in high doses may interfere with absorption of iron or copper.  But many studies still document achieving greater benefits with combined, rather than single, micronutrients therapy but many more studies are required to evaluate these interactions in malnourished populations. Because of the possibility that there may be multiple deficiencies in pregnant women in developing countries, UNICEF has concluded that a multivitamin–mineral supplement should be given during pregnancy20. By simply supplementing, many complications in the mother and infant during and after pregnancy may be avoided.

 

  1. Centers for Disease Control. Recommendations for the use of folic acid to reduce the number of cases of spina bifida and other neural tube defects. MMWR 1992;41(No. RR-14)
  2. Mahomed K. Iron supplementation in pregnancy. The Cochrane Database of Systematic Reviews 1999, Issue 4. Art. No.: CD000117. DOI: 10.1002/14651858.CD000117.
  3. Hallberg L. Bioavailability of dietary iron in man. Annu Rev Nutr 1981;1:123-47.
  4. Skikne B, Baynes RD. Iron absorption. In: Brock JH, Halliday JW, Pippard MJ, Powell LW, eds. Iron metabolism in health and disease. London, UK: W.B. Saunders, 1994:151-87. Bothwell TH. Overview and mechanisms of iron regulation. Nutr Rev 1995;53(9):237-45.
  5. Bothwell TH. Overview and mechanisms of iron regulation. Nutr Rev 1995;53(9):237-45.
  6. Siegenberg D, Baynes RD, Bothwell TH, et al. Ascorbic acid prevents the dose-dependent inhibitory effects of polyphenols and phytates on nonheme-iron absorption. Am J Clin Nutr 1994;53:537-41.
  7. Centers for Disease Control. Recommendations for the use of folic acid to reduce the number of cases of spina bifida and other neural tube defects. MMWR April 03, 1998 : 47(RR-3);1-36
  8. Mahomed K , Gülmezoglu AM. Maternal iodine supplements in areas of deficiency. The Cochrane Database of Systematic Reviews 1997, Issue 4. Art. No.: CD000135. DOI: 10.1002/14651858.CD000135
  9. Conradt A, Weidinger H and Algayer H. Magnesium therapy decreased the rate of intrauterine fetal retardation, premature rupture of membranes and premature delivery in risk pregnancies treated with betamimetics Magnesium 4, 20-28, 1985.
  10. Spatling L and Spatling G. Magnesium supplementation in pregnancy: a double blind study British Journal of Obstetrics and Gynecology 95, 120-, 1988.
  11. Sibai BM, Villar L and Bray E (1989) Magnesium supplementation during pregnancy. A double-blind randomized controlled clinical trial American Journal of Obstetrics and Gynecology 161, 115-119.
  12. Chien PFW, Khan KS and Arnott N (1996) Magnesium sulphate in the treatment of eclampsia and pre-eclampsia: an overview of the evidence from randomized trials British Journal of Obstetrics and Gynecology 103, 1085-1091.
  13. Weaver, K.: A possible anticoagulant effect of magnesium in preeclampsia; in Cantin, Seelig, Magnesium in health and disease, pp. 833-838 (Spectrum Press, New York 1980).
  14. Conradt, A.; Weidinger, H.; Algayer, H.: Magnesium therapy decreased the rate of intrauterine fetal retardation, premature rupture of membranes and premature delivery in risk pregnancies treated with betamimetics. Magnesium 4: 20-28 (1985).
  15. Kuti, V.; Balazs, M.; Morvay, F.; Varenka, Z.; Székely, A.; Szücs, M.: Effect of maternal magnesium supply on spontaneous abortion and premature birth and on intrauterine foetal development: experimental epidemiological study. Magnesium- Bull. 3: 73-79 (1981).
  16. Hunt, S.M.; Schofield, F.A.: Magnesium balance and protein intake level in adult human female. Am. J. clin. Nutr. 22: 367-373 (1969).
  17. Connor, William E., et al. Increased docosahexaenoic acid levels in human newborn infants by administration of sardines and fish oil during pregnancy. Lipids, Vol. 31 (suppl), 1996, pp. S183- S87
  18. Agostoni, Carlo, et al. Docosahexaenoic acid status and developmental quotient of healthy term infants. The Lancet, Vol. 346, September 2, 1995, p. 638
  19. http://cochranelibrary-wiley.com/doi/10.1002/14651858.CD008873.pub3/full
  20. UNICEF (1999) Composition of a multi-micronutrient supplement to be used in pilot programmes among pregnant women in developing countries.

MINIMALLY INVASIVE SURGERY IN PREGNANCY

Five years ago, on her first pregnancy, I diagnosed  Mrs. J., with a 7×7 cm ovarian cyst. On her 4th month, an exploratory laparotomy was contemplated for the removal of the ovarian cyst. Her abdomen was cut open, way bigger than the usual, to be able to expose the pregnant uterus and at the same time, manipulation of the ovarian mass located behind the uterus. With this much bigger incision, the uterus with the delicate fetus inside was held forward by an assistant while I worked behind to remove the tumor. The scar stretched as the pregnancy grew to term. The pregnancy progressed without any problems and she delivered by spontaneous vaginal delivery to a healthy baby boy, who, 5 years later manifested with exceptional IQ. The surgery, however left the mother with a midline scar running up to her umbilicus, and going around it as shown in Fig 1.

Five years later, Mrs. J. refers an acquaintance, also pregnant for the first time at 16 weeks, with a 7×7 cm. ovarian cyst.  By this time, the technology of minimally invasive therapy through laparoscopy had come of age. I convinced the patient that laparoscopic removal was the best to do in this case. Three 1-cm incisions were made on the abdomen above the level of the umbilicus, the mass was visualized, excised and later evacuated by slightly enlarging the right hole where the instruments were being inserted. It was almost like removing a tennis ball through a keyhole.

Intraoperatively and postoperatively, the patient received no tocolytic medications to prevent premature labor.  She never manifested with premature contractions post-op. The baby was monitored until the patient was discharged the following day in good condition. The patient  and her whole family were extremely amazed and grateful for her small incisions and remarkable post-op recovery.

What is Minimally Invasive Surgery or Laparoscopy?

In non-pregnant women, laparoscopic removal of ovarian cysts involves making a 1-cm incision in the umbilicus, inserting a tube telescopic rod attached to a video camera and a fiberoptic  light source. Carbon dioxide gas is then used to blow up the abdomen much llke a balloon to lift the abdominal wall from the intestines and create a working space. This gas is natural to the human body and is later absorbed and eventually removed by the respiratory system. Two other incisions are made on the left and right side of the lower abdomen to insert ports under camera guidance. This is where the instruments like graspers, scissors, etc are inserted into the abdominal cavity. Then, through a tv monitor to which the camera image of the abdominal cavity is seen, the surgery is accomplished with the instruments as a remote extension of the surgeon’s hands.

In pregnancy, the incision is made midway between the umbilicus and the lower tip of the breastbone to provide clearance to the uterus to insure that the pregnancy will not be injured upon entry of the ports and instruments.

WHAT ARE THE ADVANTAGES?

  1. Dramatically smaller scar, therefore, less post-operative pain and less need for pain medications.1
  2. Less hemorrhage thus reducing the chances of blood transfusion
  3. Less chances for wound infection due to reduced exposure of internal organs to possible external contaminants and due to a smaller skin area traumatized and exposed to skin bacteria.
  4. Less chances of  incisional hernias
  5. Increased chances of early mobilization because of minimal pain. The patient can usually go home the following day or even on the same day.
  6. Early mobilization also reduces the chances of thromboembolic complications post-operatively
    1. (formation of a clot (thrombus) in a blood vessel that breaks loose and is carried by the blood stream to plug another vessel either in the lungs (pulmonary embolism), brain (stroke), gastrointestinal tract, kidneys, or leg))
  7. Conventional surgery for ovarian cysts in pregnancy recommends waiting for the proper window of time to perform an open surgical exploration during the second trimester of pregnancy. This was because there was a reported 12% abortion rate associated with early exploration in the first trimester and up to 40% increased risk for premature labor if surgery is done in the 3rd trimester. In contrast, research has shown that laparoscopic surgery in pregnancy may be done any time in the 1st, 2nd or early 3rd trimester without increased risk from the usual operative risks.3,1,4 Since there is less or no manipulation of the uterus, which contains inside the developing baby. This leads to less uterine irritability which leads to less chances of abortion or premature labor.8
  8. Due to decreased need for narcotic pain medications post-operatively,  there is less chance of depressing the heart rate and placental perfusion and metabolism of the fetus.
  9. Due to decreased need for narcotic pain medications post-operatively,  there is less chance of depressing the heart rate and placental perfusion and metabolism of the fetus
  10. Unlike conventional surgery where the pregnant patient is placed in a supine position, the gravid uterus places pressure on the inferior vena cava resulting in decreased venous return to the heart. This decrease in venous return results in the drop in blood pressure of the mother, reduced output of the heart by 10% to 30% and decreased flow of blood to the placenta during surgery5,6,7. In performing laparoscopic surgery, the patient may easily be kept in a left lateral recumbent position. This will shift the uterus to the left of the vena cava, thus, improving venous return and cardiac output5.6, 14.
  11. The patient can go back to work sooner.9,10,11
  12. No growth or developmental delay was found in eleven children followed up till 8 years after lap surgery on the mother12.

WHAT ARE THE RISKS COMPARED TO OPEN SURGERY?

  1. All laparoscopic surgeries are done with a double set-up. This means that should there be a complications arising in the course of laparoscopic surgery preventing the surgeon from proceeding, the surgeon may convert to an open surgery.  
  2. The most significant risks are from insertion of the initial trocar since this is usually a blind procedure. There may be blood vessel or bowel injury particularly if the patient has had a previous surgery. Blood vessel injury can result in hemorrhage that may require blood transfusion. Bowel injuries, especially if unrecognized, can lead to delayed peritonitis. 8
  3. Since carbon dioxide is insufflated into the abdominal cavity to raise the abdominal wall enough to see the abdominal organs. Upward displacement of the diaphragm with air in the abdominal cavity or pneumoperitoneum in a pregnant patient can cause a decreased lung volume and functional capacity, which may possibly impair the delivery of oxygen to the tissues and to the fetus.
  4. Very rarely, patients have sustained electrical burns unseen by surgeons who are working with  electrocautery machines, the electrodes of which leak current into surrounding tissue. The resulting injuries can result in perforated organs and can also lead to peritonitis.
  5. Patients may experience shoulder pain afterwards which can result from a pocket of CO2  gas rising in the abdomen.  This can end up pushing against the diaphragm, putting pressure on the phrenic nerve which can produce a sensation of pain extending to the shoulders and can make breathing very uncomfortable. Luckily, this phenomenon is transient and will disappear once the CO2  is absorbed by the tissues and eliminated through respiration. 13

Advanced technology has made minimally invasive surgery a preferred mode of intervention particularly for removal of benign ovarian cysts. In pregnancy, it becomes even a superior procedure compared to open surgery because of the reduced discomfort for the mother post-operatively the minimal to absence of manipulation of the uterus plus the tinier scars that are left with the patient as a reminder of her surgery during pregnancy.

 

  1. Curet, M.J., et al., Laparoscopy during pregnancy. Arch Surg, 1996. 131(5): p. 546-50; discussion 550-1.
  2. Curet, M.J., Special problems in laparoscopic surgery. Previous abdominal surgery, obesity, and pregnancy. Surg Clin North Am, 2000. 80(4): p. 1093-110.
  3. Reedy, M.B., B. Kallen, and T.J. Kuehl, Laparoscopy during pregnancy: a study of five fetal outcome parameters with use of the Swedish Health Registry. Am J Obstet Gynecol, 1997. 177(3): p. 673-9.
  4. Oelsner, G., et al., Pregnancy outcome after laparoscopy or laparotomy in pregnancy. J Am Assoc Gynecol Laparosc, 2003. 10(2): p. 200-4.
  5. Elkayam U, G.N., Cardiovascular physiology of pregnancy. Cardiac Problems in Pregnancy: Diagnosis and Management of Maternal and Fetal Disease, ed. G.N. U
  6. Clark, S.L., et al., Position change and central hemodynamic profile during normal third-trimester pregnancy and post partum. Am J Obstet Gynecol, 1991. 164(3): p. 883-7.
  7. Gordon, M.C., Maternal Physiology in Pregnancy, in Obstetrics: Normal and Problem Pregnancies, S.G. Gabbe, J.R. Niebyl, J.L. Simpson, Editor. 2002, Churchill Livingstone: Philadelphia. p. 63-91
  8. Janie Fuller, DDS, (CAPT, USPHS), Walter Scott, Ph.D. (CAPT, USPHS), Binita Ashar, M.D., Julia Corrado, M.D. FDA, CDRH, Laparoscopic Trocar Injuries: A report from a U.S. Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) Systematic Technology Assessment of Medical Products (STAMP) Committee,  Finalized: November 7, 2003
  9. Andreoli, M., et al., Laparoscopic surgery during pregnancy. J Am Assoc Gynecol Laparosc, 1999. 6(2): p. 229-33.
  10. Shay, D.C., K. Bhavani-Shankar, and S. Datta, Laparoscopic surgery during pregnancy. Anesthesiol Clin North America, 2001. 19(1): p. 57-67.
  11. Oelsner, G., et al., Pregnancy outcome after laparoscopy or laparotomy in pregnancy. J Am Assoc Gynecol Laparosc, 2003. 10(2): p. 200-4.
    Elkayam. 1982, New York: Alan R Liss. 5..
  12. Rizzo, A.G., Laparoscopic surgery in pregnancy: long-term follow-up. J Laparoendosc Adv Surg Tech A, 2003. 13(1): p. 11-5.
  13. Abdominal pain after laparoscopy: the value of a gas drain. Br J Obstet Gynaecol. 1987 Mar;94(3):267-9
  14. 65. Clark, S.L., et al., Position change and central hemodynamic profile during normal third-trimester pregnancy and post partum. Am J Obstet Gynecol, 1991. 164(3): p. 883-7.
    66. Gordon, M.C., Maternal Physiology in Pregnancy, in Obstetrics: Normal and Problem Pregnancies, S.G. Gabbe, J.R. Niebyl, J.L. Simpson, Editor. 2002, Churchill Livingstone: Philadelphia. p. 63-91.
  15. Reedy, M.B., et al., Laparoscopy during pregnancy. A survey of laparoendoscopic surgeons. J Reprod Med, 1997. 42(1): p. 33-8.

 

The key element in laparoscopic surgery is the use of a laparoscope. There are two types: 1)a telescopic rod lens system, that is usually connected to a video camera (single chip or three chip) or a digital laparoscope where the charge-coupled device is placed at the end of the laparoscope, eliminating the rod lens system.[1] Also attached is a fiber optic cable system connected to a ‘cold’ light source (halogen or xenon), to illuminate the operative field, inserted through a 5 mm or 10 mm cannula or trocar to view the operative field. The abdomen is usually insufflated with carbon dioxide gas to create a working and viewing space. The abdomen is essentially blown up like a balloon (insufflated), elevating the abdominal wall above the internal organs like a dome. The gas used is CO2, which is common to the human body and can be absorbed by tissue and removed by the respiratory system. It is also non-flammable, which is important because electrosurgical devices are commonly used in laparoscopic procedures.

5-10mm diameter instruments (graspers, scissors, clip applier) can be introduced by the surgeon into the abdomen through trocars (hollow tubes with a seal to keep the CO2 from leaking).

URINARY TRACT INFECTIONS IN PREGNANCY

REBECCA B. SINGSON, M.D, FPOGS

 

Urinary tract infections (UTI) are one of the most common infections that women consult their doctor for. When you are pregnant, you are particularly more susceptible to urinary tract infections, the incidence being as high as 8 percent (8%).  

WHY ARE UTI’s MORE COMMON IN PREGNANT WOMEN?

There are several reasons for this. From the 6th week  of gestation onwards and especially during weeks 22 to 24, the higher levels of the hormone progesterone  relaxes the muscles of your ureter, (the tube connecting the kidney to the bladder) causing it to stretch and dilate in 90% of the time, a condition known as hydronephrosis of pregnancy. Your growing uterus may also compress the ureters, making it difficult for urine to flow through them as quickly and freely as it normally does. Then later in pregnancy, the baby presses on your bladder, making it hard to empty it completely when you pee. The result of these changes makes it longer for urine to pass through your urinary tract, giving bacteria more time to multiply and attach to the lining of the bladder before being flushed out.1 It also does not help that up to 70 percent of pregnant women allow sugar to pass through the tubules of the kidney (glucose is normally sieved and saved). This encourages bacterial growth in the urine; add to that the effect of increased hormones passing out through the urine like progestins and estrogens which may lead to a decreased ability of the lower urinary tract to resist invading bacteria, and you have the ingredients increased susceptibility to infection during pregnancy.

There are actually 3 clinical presentations of UTI in pregnancy: asymptomatic bacteriuria, acute cystitis and acute pyelonephritis

ASYMPTOMATIC BACTERIURIA

As much as 10% of pregnant women can actually have urinary tract infection without showing signs and symptoms.4.5 That is why it is recommended that on the 1st prenatal check-up, your doctor should subject you to a routine urine culture or urine gram stain since a urinalysis by itself may not reveal an infection. A finding of >100,000 cfu/ml with one or more organisms in two consecutive mid-stream urine specimens or one catheterized urine specimen clinches the diagnosis. 

It is important to recognize and treat asymptomatic bacteriuria during pregnancy because not doing so can have disastrous results for you. It can lead to the development of symptomatic cystitis in approximately 30 percent of the time and can lead to the development of pyelonephritis (the infection ascending to your kidneys) in up to 50 percent.4 Asymptomatic bacteriuria is associated with an increased risk of intrauterine growth retardation and low-birth-weight infants.

Treatment should be initiated once asymptomatic bacteruria is detected. The choice of antibiotic should address the most common infecting organisms and at the same time be also be safe for you and your baby. Historically, ampicillin has been the drug of choice, for UTI in pregnancy but due to increasing resistance, this drug is no longer recommended.8 Nitrofurantoin (Macrodantin) is a good choice because it is highly concentrated in the urine. Alternatively, cephalosporins such as cephalexin and cefuroxime are well tolerated and are effective in treating the important organisms. Fosfomycin (Monurol) is a new antibiotic that is taken as a single dose. Sulfonamides can be taken during the first and second trimesters but, during the third trimester, the use of sulfonamides carries a risk that your baby may develop kernicterus (brain damage from excessive jaundice), especially if your baby is premature. There are other common antibiotics that you should be extremely wary about taking while you are pregnant (e.g., fluoroquinolones and tetracyclines) because of possible toxic effects on your baby. A seven- to 10-day course of antibiotic treatment is usually sufficient to eradicate the infecting organism(s). Some authorities have advocated shorter courses of treatment–even single-day therapy. Fosfomycin is effective when taken as a single, 3-g sachet.

After completing treatment, you are required to have a repeat culture to check if bacteriuria has been successfully eradicated.

ACUTE CYSTITIS

Acute cystitis is distinguished from asymptomatic bacteriuria if you are experiencing other symptoms such as painful urination (dysuria), frequent urination (urgency), and even blood in the urine (called hematuria), without any fever or evidence of systemic illness. Up to 30 percent of patients with untreated asymptomatic bacteriuria later develop symptomatic cystitis.6  It is also vital to treat acute cystitis while you are pregnant to prevent ascent of the infection to the kidneys.

The following antibiotics are recommended for acute cystitis in pregnancy:

  • Cephalexin  250 mg two or four times daily
  • Erythromycin  250 to 500 mg four times daily
  • Nitrofurantoin  50 to 100 mg four times daily
  • Amoxicillin-clavulanic acid  250 mg four times daily
  • Fosfomycin (Monurol)  One 3-g sachet
  • Trimethoprim-sulfamethoxazole160/180 mg twice daily (to be avoided during the 1st and 3rd trimester of pregnancy)11.12.13
  • Treatment is recommended for 7-10 days because shorter treatment regimens have resulted in recurrence of infection.

ACUTE PYELONEPHRITIS

Acute pyelonephritis can occur in 2% of pregnant women and is diagnosed when the presence of bacteriuria is accompanied by fever, chills, nausea, vomiting and flank pain. Symptoms of lower tract infection (i.e., frequency and dysuria) may or may not be present. It is a serious systemic illness that can progress to maternal sepsis, preterm labor and premature delivery. Up to 23 percent of these women have a recurrence of infection during the same pregnancy.10

Early, aggressive treatment is important in preventing complications from pyelonephritis. Hospitalization, although often indicated, is not always necessary. However, hospitalization is indicated for patients who are exhibiting signs of sepsis, who are vomiting and unable to stay hydrated, and who are having contractions. However, if you are able to take oral antibiotics and there are no signs and symptoms of sepsis, you may be treated as an out-patient. Treatment duration is 14 days. 6

WHAT HAPPENS IF MY UTI REMAINS UNTREATED DURING PREGNANCY?

Not treating a UTI during gestation can have devastating maternal and neonatal complications for you. Aside from the possibility asymptomatic bacteriuria developing to cystitis which may progress to pyelonephritis, it may also lead to intrauterine growth retardation and low birth weight infants. 4.7  A study by Schieve and associates shows that the presence of UTI was associated with premature labor (labor onset before 37 weeks of gestation), hypertensive disorders of pregnancy (such as pregnancy-induced hypertension and preeclampsia), anemia (hematocrit level less than 30 percent) and amnionitis 14 While this does not prove a cause and effect relationship, randomized trials have demonstrated that antibiotic treatment decreases the incidence of preterm birth and low-birth-weight infants.15  In addition, acute pyelonephritis has been associated with anemia.16

Disastrous outcomes for your baby aside from the risk of low-birth weight may be sepsis and pneumonia (specifically, group B streptococcus infection).17,18 UTI also increases the risk of prematurity (less than 37 weeks of gestation at delivery) and preterm, low-birth-weight infants (weight less than 2,500 g and less than 37 weeks of gestation at delivery)14.

WHAT CAN I DO TO AVOID UTI?

Majority of UTIs are caused by the bacteria, E. coli, which comes from the anus, contaminating and ascending up to your bladder to cause infection. The following tips will help you therefore prevent UTIs:

  1. After a bowel movement, wash and wipe yourself in a front to back direction to prevent bacteria from the stools from contaminating the urethra. Use your forefinger and middlefinger for the vaginal area and the ring and pinky fingers for the anal area to avoid contamination.
  2. Wash with lactic acid based vaginal wash (not soap since it is the wrong ph for the vaginal) before intercourse and urinate immediately after intercourse to prevent the organism from ascending through the ureter to the bladder.
  3. Never douche during pregnancy. Not only does it mechanically remove your protective bacteria, it can be potentially fatal since it  can cause air embolism. 4. Avoid feminine sprays or powders and soaps that can irritate your urethra and genitals and make them a better breeding ground for bacteria. And don’t use douches during pregnancy.
  4. Never ignore your urge to pee. Keep the urine in the bladder encourages bacterial multiplication and increases the chances of the bacteria adhering to the lining of the bladder causing infection.
  5. Drink plenty of water, at least eight 8-ounce glasses a day to keep urine dilute.
  6. Drink cranberry juice. Studies show that cranberry juice can reduce bacteria levels and discourage new bacteria from taking hold in the urinary tract. (Drinking cranberry juice won’t cure an existing infection, though, so if you’re having symptoms, you still need to see your doctor immediately to get a prescription for antibiotics.) 19-20

Recommended doses range from 90 to 480 milliliters (3 to 16 ounces) of cranberry cocktail twice daily, or 15 to 30 milliliters of unsweetened 100% cranberry juice daily. 300 milliliters per day (10 ounces) of commercially available cranberry cocktail (Ocean Spray®) has been used in well-designed research.

Other forms of cranberry used include capsules, concentrate and tinctures. Between one and six 300 to 400 milligram capsules of hard gelatin concentrated cranberry juice extract, twice daily by mouth, given with water 1 hour before meals or 2 hours after meals has been used. One and a half ounces of frozen juice concentrate.21

UTIs during pregnancy are a common cause of serious maternal and perinatal morbidity. However,  with appropriate screening and treatment, you can limit its morbidity and avoid the dreaded complications.

  1. Patterson TF, Andriole VT. Bacteriuria in pregnancy. Infect Dis Clin North Am 1987;1:807-22.
  2. Mikhail MS, Anyaegbunam A. Lower urinary tract dysfunction in pregnancy: a review. Obstet Gynecol Surv 1995;50:675-83.
  3. Lucas MJ, Cunningham FG. Urinary infection in pregnancy. Clin Obstet Gynecol 1993;36:855-68.
  4. Kass EH. Pregnancy, pyelonephritis and prematurity. Clin Obstet Gynecol 4970;13:239-54.
  5. Gratacos E, Torres PJ, Vila J, Alonso PL, Cararach V. Screening and treatment of asymptomatic bacteriuria in pregnancy prevent pyelonephritis. J Infect Dis 1994;169:1390-2.
  6. The Philippine Clinical Practice Guideline on the Diagnosis and Management of Urinary Tract Infections: A Quick Reference Guide for Clinicians. Report of the Task Force on Urinary Tract Infections 1998. http://www.psmid.org.ph/vol31/vol31num1topic5.pdf
  7. Harris RE, Thomas VL, Shelokov A. Asymptomatic bacteriuria in pregnancy: antibody-coated bacteria, renal function, and intrauterine growth retardation. Am J Obstet Gynecol 1976;126:20-5.
  8. Peddie BA, Bailey RR, Wells JE. Resistance of urinary tract isolates of Escherichia coli to cotrimoxazole, sulphonamide, trimethoprim and ampicillin: an 11-year survey. N Z Med J 1987;100:341-2.
  9. Antimicrobial therapy for obstetric patients. ACOG educational bulletin no. 245. Washington, D.C.: American College of Obstetricians and Gynecologists, March 1998;245:8-10.
  10. Gilstrap LC 3d, Cunningham FG, Whalley PJ. Acute pyelonephritis in pregnancy: an anterospective study. Obstet Gynecol 1981;57:409-13.
  11. Duff P. Antibiotic selection for infections in obstetric patients. Semin Perinatol 1993;17:367-78
  12. Krieger JN. Complications and treatment of urinary tract infections during pregnancy. Urol Clin North Am 1986;13:685-93
  13. http://www.aafp.org/afp/20060915/985.html
  14. Schieve LA, Handler A, Hershow R, Persky V, Davis F. Urinary tract infection during pregnancy: its association with maternal morbidity and perinatal outcome. Am J Public Health 1994;84:405-10.
  15. Romero R, Oyarzun E, Mazor M, Sirtori M, Hobbins JC, Bracken M. Meta-analysis of the relationship between asymptomatic bacteriuria and preterm delivery/low birth weight. Obstet Gynecol 1989;73:576-82.
  16. Gilstrap LC 3d, Leveno KJ, Cunningham FG, Whalley PJ, Roark ML. Renal infection and pregnancy outcome. Am J Obstet Gynecol 1981;141:709-16.
  17. Mead PJ, Harris RE. The incidence of group B beta hemolytic streptococcus in antepartum urinary tract infections. Obstet Gynecol 1978;51:412-4.
  18. Wood EG, Dillon HC Jr. A prospective study of group B streptococcal bacteriuria in pregnancy. Am J Obstet Gynecol 1981;140:515-20.
  19. Lee YL, Owens J, et al. Does cranberry juice have antibacterial active? JAMA. 2000;283(13):1691.
  20. Avorn J, Monane M, et al. Reduction of bacteriuria and pyuria after ingestion of cranberry juice. JAMA. 1994;271(10):751-754.
  21. http://www.mayoclinic.com/health/cranberry/NS_patient-cranberry

TEEN PREGNANCIES

By: REBECCA B. SINGSON, M.D, FPOGS

The sexual revolution has ushered in a period in which the average adolescent experiences tremendous pressures to have sexual experiences of all kind. Pinoy teens get a higher exposure to sex from the internet, magazines and tv shows, movies and other media than decades ago, yet without any corresponding increase in information on how to handle the input. So kids are pretty much left to other kids for opinions and value formation when it comes to sex. Sexual misinformation is therefore equally shared in the group.1 Parents at home and teachers in school feel equally inadequate or uneasy to discuss the topic of sex with youngsters. The problem mounts because the barkada has a more profound influence than parents do.2 and they exert pressure and expect the adolescent to conform to the rest of the them.1 In fact, female adolescents whose friends engage in sexual behavior were found to be more likely to do the same compared to those who do not associate with such peers.3 If the teen perceives her peers to look negatively at premarital sex, she was more likely to start sex at a later age.4

Statistics in the U.S. show that each year, almost 1 million teenage women–10% of all women aged 15-19 and 19% of those who have had sexual intercourse–become pregnant5 and ¼ of teenage mothers have a second child within 2 years of their first.6 In the Philippines, according to to the 2002 Young Adult Fertility and Sexuality Study by the University of the Philippines Population Institute (UPPI) and the Demographic Research and Development Foundation, twenty-six percent (26%) of our Filipino youth nationwide from ages 15 to 25 admitted to having a pre-marital sex experience. What’s worse is that 38% of our youth are already in a live-in arrangement.

The 1998 National Demographic and Health Survey (NDHS) reveals that 3.6 million of our teenagers (that’s a whopping 5.2% of our population!) got pregnant. In 92% of these teens, the pregnancy was unplanned, and the majority 78% did not even use contraceptives the first time they had sex. Many of the youth are clueless that even on a single intercourse, they could wind up pregnant.

There are many reasons why teen pregnancies should be avoided. Here’s a low down on the facts:

Risk for Malnutrition
Teenage mothers tend to have poor eating habits and are less likely to take recommended daily multivitamins to maintain adequate nutrition during pregnancy. They are also more likely to smoke, drink, or take drugs during pregnancy, which can cause health problems for the baby.7

Risk for Inadequate Prenatal Care
Teenage mothers are less likely to seek regular prenatal care which is essential for monitoring the growth of the fetus; keeping the mother’s weight in check; and advising the mother on nutrition and how she should take care of herself to ensure a healthy pregnancy. According to the American Medical Association, babies born to women who do not have regular prenatal care are 4 times more likely to die before the age of 1 year.7

Risk for Abortion
Unplanned pregnancies lead to a higher rate of abortions. In the U.S, nearly 4 in 10 teen pregnancies (excluding those ending in miscarriages) are terminated by abortion. There were about 274,000 abortions among teens in 1996.8

In the Philippines, although abortion is illegal, it would shock you to know that we even have a higher abortion rate (25/1000 women) compared to the U.S. where abortion is legal (23/1000 women). For sure, there a lot more abortions that happen in our country that are not even reported. Backdoor abortions are resorted to with untrained “hilots” with questionable sterility procedures, increasing the possibility for tetanus poisoning and other complications.

Risk For Fetal Deaths
Statistics of the Department of Health (DOH) show that fetal deaths are more likely to happen to young mothers, and that babies born by them are likely to have low birth weight.

Risk For Acquiring Cervical Cancer
The Human Papillomavirus (HPV) is a sexually-transmitted, wart-forming virus that has been implicated in causing cancer of the cervix. This is the most common cancer in women secondary to breast cancer. Women who are at increased risk for acquiring this are those who engage in sex before 18, have a pregnancy at or younger than 18, or have had at least 5 sexual partners, or have had a partner with at least 5 sexual partners. If you start sex at an early age, you have a higher likelihood of going through several sexual partners before you settle down, thus increasing your exposure to acquiring the virus and acquiring cervical cancer. The men can get genital warts from this virus and can certainly pass it on to their partners, thus increasing her risk for cervical cancer. Is that something you would want to gift to your wife with on your honeymoon? There is a way to test women (HPV Digene test) but no test for the man so you can’t know if you have it. Using the condom does not confer protection against acquiring this virus since the condom cannot cover the testes where the warts can grow and proliferate.

Risk of For You to be More Disadvantaged
Mothers who do have a teen birth are more disadvantaged, on average, than are other teens.

  • Teenage pregnancies are associated with an increased rate of delinquent behaviors including alcohol and substance abuse.
  • To begin with, majority of them belong to the low income group. Teenage births are associated with lower annual income for the mother, 80% of whom eventually rely on welfare.
  • In the U. S. , 7 in 10 teen mothers complete high school, but they are less likely than women who delay childbearing to go on to college. They are more likely to drop out of school and only about one-third obtain a high school diploma.
  • With early termination of formal education there are also limited employment opportunities.9.10 However, they have the responsibility of having to fend for their children before they even before they ever planned to. In hiring, an employer may lean towards someone without a child versus someone who is already with one just because there are more chances of absences with the latter when her child becomes sick.
  • They face greater financial difficulties and marital conflict. With a lower capacity for earning and less emotional maturity, relationships are under more stress for breaking.
  • Young unmarried mothers also face social stigmas that can have harmful
    psychological and social impact.

Risk for Your Baby to be More Disadvantaged
The children of teen moms also face negative health, cognitive, and behavioral outcomes.3 This may result from lack of maturity, and emotional quotient or simply from ignorance due to a lack of life’s experiences

  • Children born to teenage mothers are less likely to receive proper nutrition, health care, and cognitive and social stimulation. As a result, they may have an underdeveloped intellect and attain lower academic achievement.
  • Children born to teenage mothers are at greater risk for abuse and neglect.
  • Boys born to teenage mothers are 13% more likely to be incarcerated.
  • Girls born to teenage mothers are 22% more likely to become teenage mothers.

WHAT ARE THE DETERRENTS TO TEEN PREGNANCY?

  1. Keep them at home with an intact family set up. The social institutions surrounding the youth jointly form a web of influence that either shield or lay them open to the lure of sexual risk-taking. The family is one such social institution. An intact family with both parents raising the child was found to be correlated to less risk taking behavior by teens. Those who left home early or were raised by separated parents were noted to engage in sex early and other risk taking behaviors. Family supervision and a stable parental union are definitely associated with lesser chances of engaging in premarital sex.11
  2. Keep them in school. The other social institution that shields the youth from engaging in risk taking behavior is the school.
    Leave school at an early age are more likely than other women to have their first sexual experience outside of marriage. 12
  3. Keep talking to them. Increased parental communication consistently predicted a decrease in the likelihood of young Filipinos to engage in sexual risk-taking activities. 13 It has been found that the mother, in particular has a special role because monitoring by the mother as well as communication lines with her daughter were found to be associated with less frequent intercourse and fewer sexual partners.14
  4. Keep them morally and spiritually grounded. Over 80% of the 502 teens in the September poll told re-searchers that religion is important in their lives. Regardless of gender or race, survey results revealed that teens who attend religious services frequently are less likely to have permissive attitudes about sex. 15 Orienting them with the proper values early helps them imbibe it in their lives and keeps them from succumbing to peer pressure.

    Preventing teen pregnancies requires a concerted effort on the part of the parents, the school and government to insure the right information is transmitted to the children even during their pre-teen years and insuring that they are well-monitored and supported emotionally and psychologically. We can’t watch what our kids do all the time, but then again, we won’t have to if they are equipped to make better decisions for themselves.

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  2. Ujano-Batangan, Maria Theresa D. “The Context of Sexual Risks among Filipino Adolescents: A Review of Literature.” Philippine Population Review 2 (1): 1-21.
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  5. AGI, Teenage pregnancy: overall trends and state-by-state information, New York: AGI, 1999, Table 1; and Henshaw SK, U.S. Teenage pregnancy statistics with comparative statistics for women aged 20- 24, New York: AGI, 1999, p. 5.
  6. Kalmuss DS and Namerow PB, Subsequent childbearing among teenage mothers: the determinants of a closely spaced second birth, Family Planning Perspectives, 1994, 26(4): 149-153 & 159.
  7. http://www.womenshealthchannel.com/teenpregnancy/index.shtml
  8. AGI, Teenage pregnancy: overall trends and state-by-state information, New York: AGI, 1999, Table 1; and Henshaw SK, U.S. Teenage pregnancy statistics with comparative statistics for women aged 20- 24, New York: AGI, 1999, p. 5.
  9. Werner-Wilson, Ronald Jay 1998 “Gender Differences in Adolescent Sexual Attitudes: The Influence of Individual and Family Factors.” Adolescence 33 (131): 519-531.
  10. East-West Center 2002 The Future of Population in Asia. Honolulu, Hawaii: East-West Center.
  11. Cruz, Grace T., Elma P. Laguna and Corazon M. Raymundo
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  12. Choe, Minja Kim, Hui-Sheng Lin, Chai Podhista and Corazon M. Raymundo
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  15. http://www.basapa.com/virola-of-national-statistics-4800-babies-born-per-day-in-the-philippines/