Antibody positve screen in an Rh- 29 y/o P1 - PowerPoint PPT Presentation

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Antibody positve screen in an Rh- 29 y/o P1

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Antibody positve screen in an Rh- 29 y/o P1 Scott Ikeda 9/23/08 Obstetrics Rotation Admission Data 29 y/o G6 P1041 _at_ 380 weeks by LMP (12/24/07) c/w 27 wk sono. – PowerPoint PPT presentation

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Title: Antibody positve screen in an Rh- 29 y/o P1


1
Antibody positve screen in an Rh- 29 y/o P1
  • Scott Ikeda
  • 9/23/08
  • Obstetrics Rotation

2
Admission Data
  • 29 y/o G6 P1041 _at_ 380 weeks by LMP (12/24/07) c/w
    27 wk sono. EDD 9/29/08. Pt c/o LOF at 11pm,
    clear, with ctrx q10 min, now q4 min. FM, -VB.

3
Admission Data Contd
  • PN Issues/Care
  • No prenatal visit records in EPF or ASObgyn,
    however labs and sonograms available. Pt did not
    bring records with her.
  • Rh negative s/p Rhogam 25 weeks
  • PN Labs
  • O- Ab-, GCT 132 --gt GTT 75/153/124/114 no record
    of pap, GC/Chlam all others wnl
  • Sono
  • 4 sonos btwn 272 weeks and 372 weeks, all c/w
    LMP, AFV wnl, no anatomic anomalies seen.
    However, fetus was noted to be gt97 for weight,
    last EFW at 372 weeks 3879g.

4
Admission Data Contd
  • POBHx
  • 2003 7.5lb F, NSVD, term, no complications
  • 2005 SAB
  • 2006 TOP with DC, SAB
  • 2007 TOP with DC
  • PGynHx
  • Menarche _at_ 14, irreg. avg 28d/1-2d no h/o f/c/p
    abnl pap in 2004, HPV ? LEEP 2005 no h/o STI
    except HPV.

5
Admission Data Contd
  • PMedHx
  • No asthma, HTN , DM
  • PSurgHx
  • None, except DC noted previously
  • Allergies
  • NKDA
  • Meds
  • None
  • SocHx
  • No tob/etoh/drugs, in college for Med. Asst.,
    works in sales, lives w/ mother and sister, FOB
    involved, unplanned preg
  • Fam Hx
  • Non-contributory

6
Phys Exam
  • BP 130/71, P73, R20, T98.4
  • FHR 130s baseline, mod var, -accels, -decels
  • Toco q2-3 min
  • SVE 5/90/-1
  • EFW 3900, vertex by sono
  • CV, Pulm, Abd exams wnl, trace LE edema b/l

7
Assessment Plan
  • 29 y/o P1 at 380 weeks, here for SROM at 11pm.
  • Admit to LD, collect routine labs
  • FEN/GI NPO except ice, IVF at 125cc/hr D5LR
  • Fetal status overall reassuring, EFW 3900,
    vertex. Continue EFM.
  • Labor Active labor, adequate pelvis. Expectant
    mgmt, anticipate NSVD.
  • GBS Negative. No tx indicated.
  • O-, Ab- may need Rhogam post partum pending
    fetal assessment.
  • Pain requesting epidural, anesthesia aware

8
LD Course
  • 5am - 6-7/90/-1, due to lack of progress, IUPC
    placed to measure adequacy of ctrx
  • 615am - O-, Ab, ctrx indadequate, no change in
    SVE, reassessed as latent/early active labor,
    pitocin started, antibody ID sent
  • 845a - rim/0
  • 930a - FD/0, began pushing
  • 1041a- NSVD, male, 4285g midline episiotomy,
    McRoberts suprapubic pressure.
  • Antibody ID Anti-D due to Rhogam. Neonate B-,
    Direct Coombs -

9
Rh Alloimmunization
  • Nomenclature ABO blood type plus Rh(D), Rh(D)-
  • Rh, Rh- commonly used but technically incorrect
    due to other types of Rh Ab (C, c, E, e) and D
    antigen variants.
  • Rh(D)- epi
  • Caucasians 15, African Americans 8,
    Indo-Eurasians 2, Native Am Eskimo 1-2,
    Basques 30-35, Finnish 10-12.
  • 60 homozygous, remainder heterozygous

10
Pathogenesis
  • Rh(D)- maternal exposure to Rh(D) RBCs
  • Main cause Transplacental fetomaternal
    hemorrhage
  • Iatrogenic causes re-using needles, mismatched
    transfusions, stem cell transplants
  • Assoc w/ SAB, TOP, ectopic preg, invasive
    in-utero procedures, fetal death, abd trauma,
    maternal hemorrhage, AGA, delivery
  • Small amounts (lt1ml) fetal RBCs cross placenta in
    nearly all pregnancies.

11
Fetal Effects
  • Hemolytic disease of the newborn
  • Maternal anti-Rh Ab crosses the placenta and
    binds to fetal RBCs
  • RBCs targeted for destruction in spleen
  • Anemia ? pallor, high output cardiac failure ?
    protein synthesis as liver shifts to RBC
    production ? edema jaundice, possible
    hepatosplenomegaly, possible neurological sx

12
Prevention
  • Blood type and antibody screen at first prenatal
    visit (USPSTF A recommendation)
  • Repeat screen at 24-28 wks gest unless FOB known
    Rh(D)- (USPSTF B recommendation)
  • Administer 300mcg Rh(D) immunoglobulin to
    unsensitized women at 24-28 wks gest
  • If Rh(D) (or weakly ) infant delivered, give
    another IG dose within 72 hours
  • Unless FOB known Rh(D)-, give IG after
    amniocentesis, SAB or TOP
  • Insufficient evidence for giving IG for other
    procedures (USPSTF). However, ACOG recommends for
    CV sampling, fetal blood sampling (A), and
    consider IG admin for threatened abortion,
    2nd/3rd trimester antenatal bleeding, external
    cephalic version, abdominal trauma (C).

13
For the Alloimmunized Patient
  • See flowchart
  • Indication for high-risk OB, or MFM specialist
    referral

14
Sources
  • American College of Obstetricians and
    Gynecologists (ACOG). Prevention of Rh D
    alloimmunization. Washington (DC) American
    College of Obstetricians and Gynecologists
    (ACOG) 1999 May. 8 p. (ACOG practice bulletin
    no. 4).
  • Hemolytic disease of the newborn.
    dynaweb.ebscohost.com.
  • Moise Jr., Kenneth. Pathogenesis and prenatal
    diagnosis of Rhesus (Rh) alloimmunization.
    www.uptodate.com.
  • U.S. Preventive Services Task Force (USPSTF).
    Screening for Rh(D) incompatibility
    recommendation statement. Rockville (MD) Agency
    for Healthcare Research and Quality (AHRQ) 2004
    Feb. 4 p.
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