Tuesday, August 3, 2010
Fetal Demise
The first case was that of a 32 y/o AA mom, G2P1, at 15wks GA. Informing mom of a likely demise on US was handled tactfully, with another provider consulted and a second opinion offered. The mom in this case was upset, but not shocked--she was in office that day because she was worried about her baby--"something isn't right".
I saw her again with the provider offering a second look--confirming still no fetal movement/cardiac activity, no signs of life. The second provider offered options. Both parents were present. It took them some time to digest the information given regarding the 3 options--watchful waiting, induction, or D&E. The provider gave them a lot to think about, then advised them they had time to talk it over before deciding. They left the room with the information they needed to consider and verbalized what they needed to do to complete the process. Both were calm, all questions they had at the time answered.
The next couple illustrated what an induction would be like. This involved a 35 y/o G3P2 at about 28 wks. They were admitted to L&D at around 0800. A plan was in place--mom was to be induced using 600 mg cytotec and infant delivered. Mom did not want any pain meds delivered as she wanted to be lucid and not "drugged up". Her statement was that this was the only time she was going to have with her baby girl, and she "wanted to make the most of it."
She actually delivered around 5 hours later. We had been worried that little one was presenting breech and that this was going to be a difficult passage. Luckily it worked out well. Little one was was tiny and fragile--650 some grams. Dad had a much harder time of it than mom afterwards. It was interesting to observe the family dynamics. Both sons, 2 1/2, and 4 were introduced to baby "J". The older one was more cognizent of what was going on but thought his sister was asleep. The littlest one responded to the emotion in the room and was cranky. Grandma was weeping, while grandpa was quieter and tried to help manage the older children. Mom in fact seemed to be at the most peace.
Also interesting was provider interaction. The nurse was very hands-on, very actively involved, where the nurse midwife had so many calls on her time that she was unable to be there much for the pt. There was a grief counselor involved, and her interaction was fairly close after the fact. It seemed as if the hospital processes were intrusive, though necessary, and made it difficult for the different professionals involved to utilize their training to the fullest. In fact the parents were contacted by mistake by the lab the next day regarding a genetic test that had been ordered. This upset the parents no end--and was a simple error due to processing the sample that had already been collected.
So what I learned--developing rapport is key. Each of the providers had a different style. Some more empathetic, some more direct--each effective in these cases. Managing the relationship helped the pt/family deal with the decisions to be made and manage their emotional reaction to the content of the information they were given.
I also learned managing my own reactions was more difficult than I expected. I did get a bit teary-eyed. I did get a lump in my throat. When I was talking to the mom while she was holding her infant I did have to work at it a little bit. Dad was a bit easier, but mostly that was because I kept expecting him to pass out and I was ready to help keep him from falling and hurting himself.
The managing my inner self bit has been a theme this semester at least--keeping an open mind, giving pts the opening without leaping to conclusions... People don't always react the way you'd expect.
Monday, August 2, 2010
Torn between Molluscum contagiosum and Gardasil vs. HPV
I was going to talk here about the 18yo female who had her Gardasil 3-shot series, before she had any sexual activity (per her report), and still ended up with an ASCUS PAP with HPV-having to discuss with her how there are over 100 HPV strains and the Gardasil only protects against 4 types and she still needed to use condoms or abstinence to decrease possible transmission of other HPV types.
The papules are about 2 - 5 millimeters wide. There is usually no inflammation and subsequently no redness unless you have been digging or scratching at the lesions. The skin lesion commonly has a central core or plug of white, cheesy or waxy material. In adults, the lesions are commonly seen on the genitals, abdomen, and inner thigh.
Molluscum contagiosum is a harmless virus but it may persist for months or occasionally for a couple of years. It frequently induces a type of dermatitis in the affected areas, which are dry, pink and itchy. Molluscum contagiosum may rarely leave tiny pit-like scars.
Non-medicine treatment- the infection can be cleared without medicine if there are only a few lesions as there were in our 2 patients at the clinic (each had less than 10 total). First, the affected skin area was cleaned with an alcohol swab. Next, a sterile angiocath needle was used to cut across the head of the lesion, through the central dimple. The contents of the papule (the central cheesy core) was removed with another alcohol swab. This procedure was repeated for each lesion (and is therefore unreasonable for a larger infections). With this method, the lesions would heal in two to three days. There was minimal pain with each molluscum core removed.
Lesions may resolve spontaneously without any treatment and without scarring within 6 to 12 months but may take as long as 4 years to completely disappear. Other treatment options include use of caustic chemicals (podophyllin, trichloroacetic acid, silver nitrate), lasers, and/or cryotherapy (liquid nitrogen). These options require a trained health care provider, may require local anesthesia, and can result in pain, irritation, and scarring. If every lesion is not removed, the condition may recur. Infected persons should return for reexamination one month after treatment so any new lesions can be removed. Sex partners should be examined for signs of infection as well.
Molluscum Contagiosum at a Glance
• Very common, contagious, benign skin disorder
• Caused by poxvirus
• Often seen in otherwise healthy people
• Commonly affects children and sexually active adults
• Typically on the trunk arms, and legs
• Looks like scattered, small, smooth tan or pink bumps
• Easily curable in most cases
• Sometimes clears on its own without treatment
• May require multiple treatments and ongoing maintenance therapy
• Often treated with freezing with liquid nitrogen
Prevented by good skin hygiene
http://lagunaskincenter.com/molluscum.aspx
Sunday, August 1, 2010
There is a reason this is forbidden
greg
Thursday, July 29, 2010
"He just gets pushy"
We can all appreciate the depth and breadth of inquiry during an initial OB visit...which, should be answered as best as possible by the WOMAN....well, during the interview with this particular visit, L.Z. for some reason, allowed her boyfriend/father of baby of 6 months to answer most of the questions because, as he put it, " [she] was taking too long to answer the simple questions."
He was so blatantly verbally aggressive in the exam room, that I feared how he might behave towards her when not in public or if there was actually a "real" dispute between the them. So when he volunteered his excuse from the room to allow her physical exam to be conducted, I brought it down...tactfully and professionally as possible my concerns about her safety, the safety of her unborn baby as the pregnancy ensues and the overall safety and welfare of her and the baby after delivery. Though she became teary eyed, she insisted that he had never been physically, emotionally, sexually, or otherwise abused by him nor felt threatened for her life or safety. She simply stated, "He just gets pushy." I expressed to her, again, my concerns for her during the pregnancy and discussed the recency of their relationship and pregnancy state and potential for the verbal aggression to escalate to physical violence. I provided her with multiple numbers for support and counseling that we hand wrote on a sticky pad so as not to raise alarm to her boyfriend if he saw pamphlets or handouts specifically addressing the concerns. We thoroughly documented the encounter and instructed her to schedule a visit, ALONE, within the next week and if she didn't mind, to keep the provided informed if she was seeking counseling or assistance she sought so as to ensure her optimal safety throughout the pregnancy. We did not contact her command as there was no evidence of physical abuse on exam and she vehemently denied being abused. Her boyfriend was not AD and thus this would otherwise be purely domestic requiring involvement of local law enforcement if things escalated. Moral of the story, never be afraid to ask, never be afraid to offer, never ignore your gut instinct that something is wrong. She expressed sincere gratitude for recognizing his behavior as she admitted feeling "stressed" by it...ding, ding, ding!!! and that she would follow through with scheduling her follow-up.
Waterbirthing
More research needs to be completed but up until now preliminary evidence supports shortening of the first stage of labor, better pain control (decreased analgesia), decreased interventions by healthcare providers, provides a gentler transition for infant to extra uterine life, and empowers mom to be more in control of the birthing process
Some concerns are related to infection control; exposure to blood, feces, and meconium, increased staffing required to safely monitor patients and equity for non-waterbirthing moms, Airway safety/aspiration risks. Finally stategies related to training, protocols, and CPG's.
This is an old and ongoing debate as this is not new, yet I found interesting the facility did not have prior to the actual installation of unit.
Check out www.waterbirthing .org , jump in the water is fine!
Centering
Centering is copyrighted program and the individual institution is required to pay for the privilege of incorporating Centering as a program offered by their clinic. Facilitators must participate in a 2 day work shop prior to leading a centering group.
In addition to the group interaction, and education each woman is assessed by the OB provider, and appropriate checks in cluding fundal height, fetal heart tones are performed at each class, with additional assessments cervical checks, and ultra sounds perfomed indiiually as required and or necessary.
The program incorporates self evaluations from participants who provide feedback. MACH is not currently conducting additional surveys or research to evaluate the programs effectiveness as compared to traditional prenatal care or to other prenatal classes.
The class of seven women which I observed seemed to be very effective in that all of the participants appeared to share information and advice openly but not so much as to be overbearing. The facilitator, a CNM, presented appropriate educational materials encouraged comments from the participants about what was being discussed, while allowing and encouraging participants to be fully involved in the class. Private time for assessment was provided in a way which was discrete and which did not detract from the overall flow and development of the day’s class.
Overall I found that I was impressed by the process and the individual participants seemed to be well satisfied. The advantage of this program for military personnel is that it excellent forum for discussion and sharing of pregnancy related issues along with personal support for women who are often remote to their natural family support systems
Tuesday, July 27, 2010
An expert opinion doesn't replace human kindness
When the pt returned, her values had improved accordingly and the more detailed ultrasound showed a viable fetus around 6wks. I shudder to think of what harm we could have caused by just following the expert, some life situations require us to pause and take a breath not forgetting to impart some human kindness.
Monday, July 26, 2010
What is that???
A 32 y/o G2P2L2 white female, 4 weeks postpartum s/p uncomplicated SVD with epidural presented to the acute care clinic with chief complaint of “blood clot inside labia”. States she noticed a dark red lesion inside her labia that morning. Denied pain, but c/o itching. Denied drainage from lesion, dysuria, hematuria, urinary difficulties, or vaginal discharge. Denied shaving, intercourse, or other trauma. Currently breastfeeding. On inspection and palpation, there was a 1cm x 1cm round, swollen, red, inflamed protrusion in the between the labia minora, covering the urethra and extending to the inferior border of the clitoris. The mass was firm, immobile, and nontender with palpation.
This image above is similar to what I saw.
I wasn’t exactly sure what the lesion was, but the provider immediately recognized it and diagnosed her with urethral prolapse. Urethral prolapse is not a common condition and is often misdiagnosed. Most cases occur in pre-menarchal and post-menopausal women and is thought to be caused as a result of trauma or lack of estrogen causing laxity of the pelvic floor. Our patient probably had multiple factors that contributed to her development of urethral prolapse. Trauma s/p foley catheterization and vaginal delivery and lack of estrogen induced by breastfeeding in the post partal period probably all played a part. Because the condition is uncommon, there is not a clear consensus about treatment, but options include manually replacing the prolapse, estrogen creams, kegels, physical therapy, and surgery. As our patient had a mild prolapse without signs of urinary obstruction, we opted for less aggressive treatment and prescribed estrogen cream and recommended kegels. So if you happen to see a post partum patient with an odd vulvar lesion, keep urethral prolapse in your differentials.
Saturday, July 24, 2010
I'm in the Brig!
Friday, July 23, 2010
I thought this was women's health!
36 yo AA G2P2A0 WWE
Interesting Issue_Delgado
34yo G1P0 presents for NOB visit. She is originally from Thailand and does not speak English very well. Her husband is due to deploy to Afghanistan in November. When he leaves she will have no support system within the United States. During this visit we had to handle the psychosocial problems and family health concerns. You could tell the patient and spouse were very distraught on what the future may hold. This was her first pregnancy and she would have the child in a foreign country without her husband and she already had problems communicating her concerns. The couple believes that the best course of action was to have the patient stay in Thailand with her family once he had left for his deployment; however, they mentioned that Tricare was giving them a hard time because “she had to stay within the region he was assigned or they wouldn’t pay for medical expenses”. The couple wanted to ask our opinion on how to handle the situation. We told them that we could not tell them what to do; however, if she was to move in November she would be leaving around 28 wks gestation. So, a majority of her OB management would still be able to be performed at Bethesda.
Thursday, July 22, 2010
Can anyone say TBI???
Friday, July 16, 2010
Sometimes you don't want to know the answer
Rash during pregnancy
31y/o Caucasian female ADAF G1P0 30.5 weeks. Was seen by WHNP for ROB. Patient had rash on abdomen/back diagnosis tinea and pt given fungal topical and dermatology referral. Patient had no improvement with fungal cream and lesions progressed to vesicles when derm provider assessed her. When patient presented to dermatology her rash had also spread to soles of feet, feet, arms, hands and all sections of her chest, abdomen and back. Patient was started on topical steroid by derm provider and lesion biopsies obtained. Differential diagnosis included Pemphigoid gestationis (he was pretty sure this would be confirmed by biopsies as patient was classic presentation per his reference text). I saw patient with OB MD. Preliminary biopsy results were available and they were not consistent with diagnosis of pemphigoid gestationis; “had eosinophilic characteristics”. Patient diagnosis dermatitis; current biopsies to be sent to AFIP for second opinion, Vistaril 100mg po q6h for sleep and continue topical steroid for lesions. Topical steroid seemed to be working—size of lesions was decreasing and fewer vesicular lesions observed. She had previously tried OTC Benadryl but it did not provide pain relief or help her sleep. Patient to start NSTs twice a week. OB provider to consult with dermatology to ensure biopsies were correctly collected (couldn’t be placed in formalin for this diagnosis). Patient was still having a hard time sleeping and even walking because of the lesions on her feet or those rubbing on her uniform. She was the last patient I saw during my rotation and I do not know her definitive diagnosis.
Pemphigoid gestationis (Medscape, 2010)
Pemphigoid gestationis (PG) is a rare autoimmune bullous dermatosis of pregnancy. The disease was originally named herpes gestationis on the basis of the morphological herpetiform feature of the blisters, but this term is a misnomer because pemphigoid gestationis is not related to or associated with any active or prior herpes virus infection.
Pemphigoid gestationisis a pregnancy-associated autoimmune disease. Most patients develop antibodies against 2 hemidesmosomal proteins, BP180 (BPAG2, collagen XVII) and less frequently BP230. Historically known as herpes gestationis factor, these circulating antibodies belong to the heat-stable immunoglobulin G1 subclass. The binding of immunoglobulin G to the basement membrane triggers an immune response, leading to the formation of subepidermal vesicles and blisters. The trigger for the development of autoantibodies in persons with pemphigoid gestationis remains elusive. Cross-reactivity between placental tissue and skin has been proposed to play a role. Pemphigoid gestationis has a strong association with HLA-DR3 (61-80%) and HLA-DR4 (52%), or both (43-50%), and virtually all patients with a history of pemphigoid gestationis have demonstrable anti-HLA antibodies. The placenta is known to be the main source of disparate (paternal) antibodies and can thus present an immunologic target during gestation.
In the United States, pemphigoid gestationis has an estimated prevalence of 1 case in 50,000-60,000 pregnancies.
International
Findings from European studies suggest that pemphigoid gestationis has an overall incidence of 0.5 cases per million people per year. In 1999, Jenkins et al2 described the largest cohort of 87 patients in the United Kingdom with a total of 278 pregnancies, of which 142 were complicated by pemphigoid gestationis.
No increase in fetal or maternal mortality has been demonstrated. A greater prevalence of premature and small-for-gestational-age (SGA) babies is associated with pemphigoid gestationis. Of infants, 5-10% born to affected mothers may present with transient cutaneous involvement that resolves as maternal autoantibodies are cleared. Patients with pemphigoid gestationis have a higher relative prevalence of other autoimmune diseases, including Hashimoto thyroiditis, Graves disease, and pernicious anemia, which are also associated with HLA-DR3 and DR-4 haplotypes
Pemphigoid gestationis is less common among blacks than whites, which might reflect its association with specific HLA haplotypes.
This condition only affects females.
Pemphigoid gestationis occurs in women of childbearing age.
Pemphigoid gestationis typically manifests during late pregnancy, with an abrupt onset of extremely pruritic urticarial papules and blisters on the abdomen and trunk. Unrelenting pruritus often interferes with daily activities. Lesions may appear any time during pregnancy, but they most commonly develop during the second and third trimesters.Symptoms may abate at the end of pregnancy; however, dramatic flares can occur at or immediately after delivery. Pemphigoid gestationis usually resolves spontaneously within weeks to months after delivery and possibly quicker with breastfeeding. The persistence of disease activity for years postpartum has been reported. Pemphigoid gestationis may recur with the resumption of menses, use of oral contraception, and subsequent pregnancies. The 1999 cohort study by Jenkins et al2 showed no association between change in partner and development of pemphigoid gestationis in subsequent pregnancies.
The initial clinical manifestations are erythematous urticarial patches and plaques, which are typically periumbilical. These lesions progress to tense vesicles and blisters. Some patients may present with urticarial plaques and may never develop blisters (see the images below). These hive-like plaques differ from true urticaria because of their relatively fixed nature. The rash spreads peripherally, often sparing the face, palms, and soles. Mucosal lesions occur in less than 20% of cases. Patients may have secondary infections at blister sites.
Differential Diagnoses
Bullous Pemphigoid
Cicatricial Pemphigoid
Linear IgA Dermatosis
Pruritic Urticarial Papules and Plaques of Pregnancy
Urticaria, Acute
Other Problems to Be Considered
Allergic contact dermatitis
Dermatitis herpetiformis
Drug-induced bullous disorders
Erythema multiforme
Papular dermatitis of pregnancy
Prurigo gestationis of Besnier
Pruritic folliculitis of pregnancy
Routine laboratory studies are not helpful in diagnosing pemphigoid gestationis. The results with most hematologic studies are within normal limits, although peripheral eosinophilia is not uncommon and may correlate with disease severity. Laboratory values that may be elevated include immunoglobulin levels, erythrocyte sedimentation rates, acute phase reactant levels, and antithyroid antibodies.
The criteria for the diagnosis of pemphigoid gestationis include an appropriate clinical presentation, histologic findings of a subepidermal blistering process (as described below), and direct immunofluorescence (DIF) results that show a linear band of C3 deposition with or without immunoglobulin G (present in 20-25% of patients) along the basement membrane. The DIF test is the key assay to differentiate pemphigoid gestationis (positive DIF findings) from pruritic urticarial papules and plaques of pregnancy (negative DIF findings). However, a similar pattern of DIF results is observed in patients with pemphigoid gestationis, BP, and epidermolysis bullosa acquisita (EBA). DIF should be performed using samples from noninvolved perilesional skin.
http://emedicine.medscape.com/article/1063499-overview (for pictures and more detail)
Thursday, July 15, 2010
Contraception Issues
Another case was a 24 year old G1P1 female who came in because she was interested in starting new contraception. She reported that she had tried an oral contraceptive in the past with good results and she had only come off to have her child. During the interview, the patient revealed that she has very heavy menstrual cycles every month and the oral contraceptives never seemed to help that much. After talking with the patient, I thought that she would benefit from the Mirena IUD. So, I started discussing the risks and benefits with her and she was on board until I mentioned that the Mirena could help decrease her menstrual flow and in time may even stop her period. She then commented that it is "not natural" for a woman to not have a period and that she would rather have heavy cycles than not have a period. No amount of education from us could change her mind, so we prescribed the oral contraceptives. It was just interesting to see these two patients with such strong viewpoints on contraception.
Tuesday, June 15, 2010
Interesting case - HELLP?
Abnormal Labs:
Lactate dehydrogenase 245 (108-212)
Serum uric acid 6.2 (2.3-5.6)
Bilirubin 0.1 (0.2-1.0)
RBC 3.07 (4.0-5.2)
Hgb 9.1 (12-16)
Hct 27.8 (35-46)
Platelets normal at 379
LFTs WNL
Plan:
BP checks x 5days in clinic or at CVS/Walgreen’s; come to clinic if over 160/110
Atarax for itch
Hydrocortisone cream for rash
Adalac CC for elevated BP
I found this case interesting because my first thought was HELLP; however, the labs did not support this diagnosis, although the enlarged liver and RUQ pain can be symptoms of HELLP. I was surprised to see the normal LFTs. The HTN could indicate pre-eclampsia. My preceptor stated that the edema is not unusual post partum because of all the IV fluids administered during labor (3-4 liters). As far as the rash goes, I don’t think it was related to the other symptoms. There are many causes for elevated lactate dehydrogenase including hemolytic anemia, infectious mononucleosis, and liver disease but I couldn’t find anything to indicate that this elevation could be a result of having given birth 8 days ago. Obviously, my preceptor was more comfortable than me in treating this woman conservatively. The enlarged liver still bothers me.
Monday, June 14, 2010
INTERESTING ISSUE-Susan Frisbie-13 June 2010
Twenty-nine year old, G3P3003, Caucasian female presents for six week postpartum appointment. The interesting piece is she is a surrogate mother for a civilian couple. The gametes were fertilized outside the womb, in vitro. She came alone to the postpartum appointment because her husband is deployed. However, he did come for the delivery. Do you wonder what her depression scale score was? It was a three and she was in good spirits. She chose to breastfeed the baby while in the hospital and I thought it was a little odd. The baby left the hospital with the adopted parents. The patient receives almost daily texts with photos of the baby. This is her first time being a surrogate mother and she states she would do it again. She and her husband are happy and have two children of their own. Thoughts that come to my mind….. Tricare will not pay for in vitro but I bet the prenatal care is covered. So is it legal for an active duty member to be a surrogate? If the DoD is aware of the intent for surrogacy will Tricare cover the cost of prenatal care and the delivery? Also found it interesting that Tricare will not cover surrogacy as an infertility option.
Amniocentesis or Not???
One day I had the opportunity to spend the morning with a Genetics Counselor. We had a 42-year old patient present to the clinic with her spouse. She has had 8 miscarriages in the past (with 3 being in the 2nd trimester). She is now 18 weeks pregnant again and been told that her quad screen came back positive for Trisomy 18. So now we have a few issues here. The woman is AMA and she now has a positive Quad Screen and she also has a family history of miscarriages to include her sister and mother. The Genetics counselor explained to her that the reasons for all the miscarriages were more likely due to genetics/chromosomal abnormalities. The patient had a ROB prior to arriving to her appointment with the genetics counselor and was never told of her Quad Screen results until her appt with us. The patient denied any reason to believe what the genetic counselor was saying to be true. The Genetics Counselor recommended the patient receive an US as well as Amniocentesis. The counselor told the patient and her husband that the benefits of her going through with it. She also talked to the patient about the risks, which included miscarriage. The patient, concerned, began to speak about going through with it, when the spouse interrupted and stated that he definitely did not want any counseling to be done. He mentioned that they have gone through a lot with these past 8 miscarriages and have even sought treatment with the infertility clinic in Virginia and also having a cervical cerclage to ensure that she could maintain the pregnancy in case that was the issue for all her miscarriages. Both parents agreed not to do any further testing to include refusal of an Ultrasound. The patient stated that she believed that her God would provide for them a healthy baby boy and that she did not need to be followed up. I felt as if the genetic counselor could have been a little more sympathetic as well as informative to the patient. The patient was scared upon entry to the office and had no idea why she was even referred to the Genetic Counselors Office. So there was a lack of communication on some providers part. Then she enters this office and “boom” all of this information is thrown at her. If I were in the patients shoes, I would be extremely overwhelmed and would find it hard to maintain my composure. Here I am ecstatic about finally having a baby. Convinced that I am having this happy baby boy only to find out that I might be having a baby with Trisomy 18… Sad…..:o(