f undamentals of o bstetrics
play

F UNDAMENTALS OF O BSTETRICS Christine Pecci, MD Associate Clinical - PowerPoint PPT Presentation

F UNDAMENTALS OF O BSTETRICS Christine Pecci, MD Associate Clinical Professor UCSF Department of Family and Community Medicine March 2017 No disclosures O BJECTIVES Describe the group prenatal care model Review criteria for


  1. F UNDAMENTALS OF O BSTETRICS Christine Pecci, MD Associate Clinical Professor UCSF Department of Family and Community Medicine March 2017

  2.  No disclosures

  3. O BJECTIVES  Describe the group prenatal care model  Review criteria for ultrasound vs LMP dating  Review management of women at risk for preterm delivery  Describe guidelines for diagnosis, treatment and management of preeclampsia, gestational diabetes and thyroid disease in pregnancy  List infections in pregnancy and how to manage or prevent these from occurring

  4. P RENATAL CARE MODELS : DO WE KNOW WHAT ’ S BEST ?  Traditional care-ACOG  Q 4 wk visits until 28 weeks  Q 2 wk visits until 36 weeks  Q 1 wk visits until delivery  Traditional care- ICSI  8-11 visits total  6-8 wks, 10-12 wks, 16-18 wks, 22 wks, 28 wks, 32 wks, 36 wks, 38-41 wks  Group Prenatal Care  Group of 5-12 patients x 2 hours q 2-4 wks

  5. G ROUP OR TRADITIONAL PRENATAL CARE ?  Similar rates of PTD, NICU admission and breastfeeding initiation rates  African American women with significantly lower PTD rate* but not among Latina  Decreased rate of LBW overall**  No harm in doing group care and likely benefit in certain groups Carter et al OB GYN Sept 2016

  6.  Tanya is a 23 yo G1P0 who presents for early pregnancy care. EGA 10 1/7 wks by a sure LMP  She had a visit to ED for nausea and vomiting  Given 1 liter NS  Electrolytes were normal  TSH 0.1

  7. N AUSEA AND VOMITING IN PREGNANCY  Nausea in 50-80%  Vomiting/retching 50%  Hyperemesis gravidarum 0.3-3%  Persistent vomiting  Weight loss  Ketonuria  Usually electrolyte, thyroid, liver abnormalities  Lower rate of miscarriage ACOG Practice Bulletin April 2015

  8. T REATMENT OF N / V IN PREGNANCY  Multivitamin x 3 months before conception  Ginger may decrease nausea  Acupuncture/acupressure- no difference in RCTs  First line treatment pyridoxine +/- doxylamine  Metoclopromide, ondansetron second line  Limited safety data, but overall risk low  Oral corticosteroids used as last resort– avoid 1 st trimester ACOG Practice Bulletin April 2015

  9. N ORMAL T HYROID FUNCTION AND PREGNANCY  Hcg stimulates TSH receptor, increasing thyroid production and decreasing TSH  Total thyroid hormone levels increase due to elevated thyroid-binding globulin (TBG)  Free T4 unchanged ( direct assays ok but many labs use automated assays which can be inaccurate )  TSH is a reliable indicator of maternal thyroid status (American Thyroid Association)  First trimester 0.1-2.5 mIU/L  Second trimester 0.2-3.0 mIU/L  Third trimester 0.3-3.0 mIU/L

  10. H YPERTHYROIDISM IN PREGNANCY  Avoid meds in 1 st trimester  If medication needed, use PTU  risk of liver failure  Risk face and neck cysts  Consider changing methimazole after 16 wks (aplasia cutis) other congenital malformations  Smallest possible dose as medications cross placenta and can be more potent for fetal thyroid  Target: at or just above upper range of normal  Moniter TSH/T4 every 4 wks if on medication

  11. H YPOTHYROIDISM  Case control trials showed hypothyroidism associated with low IQ in the fetus  RCTs do NOT confirm that treatment of subclinical hypothyroidism improves neurocognitive outcomes  Both initiated Rx after first trimester  Universal screening for thyroid disease in pregnancy is not indicated*  Increased pregnancy loss with elevated TSH, especially if TPO ab elevated  Effectiveness of Rx not yet proven  Maybe need to screen 4-7 wks? *ACOG, Endocrine Society, American Association of Clinical Endocrinologists

  12. R ECOMMENDATIONS  Treat if TSH >10  TSH>2.5 check TPO Ab status  ?treat if TPO Ab+ and TSH >2.5  Don’t treat if TPO neg and TSH > upper nl <10  If treating  Target lower half of preg specific range or <2.5  Measure q4 wks in pregnancy then at least once near 30 wks American Thyroid Association 2017

  13. S UPPLEMENTATION AND PREGNANCY  50-85% need increase in thyroid replacement  Preconception treat to <2.5  Should increase dose by 25-30% ASAP post conception (can give two extra pills/wk)  Postpartum following delivery go back to pre- pregnancy dose and recheck in 6 wks  If Rx started in pregnancy with nl TSH reasonable to stop and recheck in 6 wks

  14. LMP VS . US DATING  Tanya also had an US done in the ED  Crown-rump length = 9 2/7 weeks  LMP 10 1/7 wks  6 days different than EDD based on LMP  Should you change her dating based on 1 st trimester US?

  15. D ATING Gestational Age Discrepancy for re-dating w US date < 9 weeks > 5 days (CRL) 9 weeks to < 14 weeks > 7 days (CRL) 14 weeks to < 16 weeks > 7 days (BPD, HC, AC, FL) 16 weeks to < 22 weeks > 10 days 22 weeks to < 28 weeks > 14 days 28 weeks and beyond > 21 days Single uniform standard based on expert opinion (ACOG, AIUM, SMFM) EDD=280 days after first day LMP Half of women accurately remember LMP 40% adjustment in 1 st trimester; 10% adjustment 2 nd trimester Use earliest US ACOG Committee Opinion Oct 2014

  16. W ILL MY BABY BE NORMAL ?  She has been reading about a new test for making sure the baby is normal. She wants to know if you can order this test. Will having a normal test guarantee that this baby will be okay?

  17. Characteristics of screening tests:T21 Dashe, Jodi MD Obstet Gyn 2016

  18. Options for screening First Trimester Second Trimester hcg + PAPP-A hcg + AFP + estradiol + inhibin 11-14 wks 15-22 wks Can be combined w NT Anatomy scan AFP in 2nd trimester for NTD Includes AFP • 1 st trimester screening gives the patient early results • 2nd trimester screening good for late entry to care • DON’T do both independently • CAN do combined (7 serum markers + NT)

  19. C OMBINED 1 ST AND 2 ND TRIMESTER SCREENING  Sequential testing Stepwise  high risk offered diagnostic testing after 1 st trimester  Others get results after second trimester Contingent  highest risk offered diagnostic testing after 1 st tri  lowest risk reassured- no further testing  Others get results after 2 nd trimester  Integrated testing

  20. C ELL - FREE DNA  Circulating DNA fragments placental in origin from apoptotic trophoblasts  Can be done anytime after 9-10 wks gestation  Available in 7-10 days  Best for trisomy 21 and 18 but also screens for trisomy 13 and sex chromosome aneuploidies  Gender  Can be used as primary or secondary screening AJOG June 2016 SMFM Consult Series

  21. Dashe, Jodi MD Obstet Gyn 2016

  22. I’ M SO NERVOUS …  Tanya is worried specifically about preeclampsia because her sister had it and needed to be induced a few weeks before her due date.  “Is there anything that you can give me so that I don’t get this disease too?”

  23. P REECLAMPSIA : Y OU WILL SEE IT !  Incidence 2-8%  Has increased by 25% in last two decades  More likely in patients with hypertension  Unrecognized has serious health consequences for mom and baby  Risk factor for future CV and metabolic disease Task Force for Hypertension in Pregnancy, 2013

  24. I NITIATE ASA 12-28 WKS FOR HIGH RISK  History of pre-eclampsia, esp if adverse outcome  Multi-fetal gestation  Chronic hypertension  Diabetes type 1 or 2  Renal disease  Autoimmune disease (SLE, APS)  Patient with history of preeclampsia <34 wks  Prevalence 40%  NNT 1:20 Practice Advisory on Low-Dose Aspirin and Prevention of Preeclampsia: Updated Recommendations July 11 , 2016

  25. C ATEGORIES  Preeclampsia-eclampsia  With or without severe features  Chronic hypertension  Gestational hypertension- hypertension without proteinuria after 20 week  Chronic hypertension with superimposed preeclampsia Task Force for Hypertension in Pregnancy, 2013

  26. P ROTEINURIA  >300 mg in 24 hrs  Spot urine:creatinine ratio > 0.3  Dipstick 1+  Proteinuria is classically part of the syndrome  But NOT required to make diagnosis of preeclampsia

  27. D IAGNOSIS  Elevated BP  >140/90 on two occasions 4 hours apart  Proteinuria or “severe features”  >160/110  Plts <100K  LFTs twice normal  Persistent RUQ pain or epigastric pain  Creatinine >1.1 or double  Pulmonary edema  New onset cerebral or visual disturbance

  28. W HEN TO DELIVER ?  Chronic hypertension  Deliver after 38 0/7 wks  Gestational hypertension:  Deliver at 37 0/7 weeks  weekly dip for proteinuria + BP check (can be at home)  NST q week

  29. W HEN TO DELIVER ?  Preeclampsia without severe features:  Deliver at 37 0/7 weeks  2x week BP, once a week labs  2x week NST  Preeclampsia with severe features  Deliver at 34 0/7 weeks  Monitor in hospital  Severe uncontrolled htn, eclampsia, pulm edema, abruption, DIC, NRFHR, IUFD  Immediate delivery after initial stabilization

  30. I NTRAPARTUM I NTERVENTIONS  Mg with severe preeclampsia only  Anti hypertensive meds only for > 160/110  Administer steroids prior to delivery

  31. P OSTPARTUM FOLLOW - UP  Check BP 72 hours post delivery and 7-10 days postpartum  Treat for >150/100 on two occasions 4-6 hrs apart  Preconception- glycemic control, weight loss  ALL patients should receive education on warning signs

Download Presentation
Download Policy: The content available on the website is offered to you 'AS IS' for your personal information and use only. It cannot be commercialized, licensed, or distributed on other websites without prior consent from the author. To download a presentation, simply click this link. If you encounter any difficulties during the download process, it's possible that the publisher has removed the file from their server.

Recommend


More recommend