Re: Placenta cultures

From: art fougner, md (evsono@pipeline.com)
Sun Apr 9 09:28:18 2006


A related issue ...

Am J Obstet Gynecol. 2004 Dec;191(6):2010-5. Are histopathologic chorioamnionitis and funisitis associated with metabolic acidosis in the preterm fetus?

Holcroft CJ, Askin FB, Patra A, Allen MC, Blakemore KJ, Graham EM.

Department of Gynecology-Obstetrics, Division of Maternal-Fetal Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

OBJECTIVE: Perinatal infection increases the risk of neonatal neurologic injury. Our objective is to determine whether histologically confirmed chorioamnionitis and funisitis is associated with fetal metabolic acidosis. STUDY DESIGN: This is a retrospective cohort study of all infants 34 weeks or less born at a single tertiary hospital admitted to the neonatal intensive care unit (NICU) between April 1999 and September 2002. Maternal and neonatal records and placental pathology reports were reviewed. RESULTS: There were 392 infants at 23 to 34 weeks' gestational age admitted to the NICU during this period of whom 354 had placental pathology reported; 259 infants had umbilical cord gases available. These neonates were placed into 3 groups: group 1 (208 infants) had no signs of placental infection, group 2 (59 infants) had isolated chorioamnionitis, and group 3 (87 infants) had both chorioamnionitis and funisitis. The gestational age (30.2 +/- 2.8, 28.3 +/- 3.4, 27.8 +/- 2.8 weeks, P < .01) and birth weight (1358 +/- 520, 1242 +/- 547, 1103 +/- 381 g, P < .01) were significantly higher in group 1. There was an increase in neurologic morbidity in groups 2 and 3 (25.2%, 34.4%, 43.7%), which was not significant when corrected for gestational age. Groups 2 and 3 had a small but significant increase in umbilical arterial pH (7.25 +/- 0.10, 7.29 +/- 0.10, 7.30 +/- 0.08, P < .01) and base excess (-3.5 +/- 3.6, -2.2 +/- 3.6, -2.3 +/- 2.7 mmol/L, P = .02). When a single pathologist reviewed all placentas with any inflammation and staged them on the basis of the degree of the fetal inflammatory response, no relationship was found between the degree of fetal inflammation and umbilical arterial pH (stage 1, 7.27 +/- 0.09; stage 2, 7.30 +/- 0.09; stage 3, 7.30 +/- 0.08; P = .41) or base excess (stage 1, -2.82 +/- 3.47 mmol/L; stage 2, -1.95 +/- 3.17 mmol/L; stage 3, -2.23 +/- 3.07 mmol/L; P = .62). When stepwise multiple linear regression was performed, neither histologic chorioamnionitis nor histologic funisitis were associated with a change in umbilical cord pH or base excess. CONCLUSION: Intrauterine infection, as confirmed by histologic chorioamnionitis and funisitis, is not associated with fetal metabolic acidosis. Intrauterine infection may represent a nonhypoxic form of encephalopathy that produces neurologic morbidity by a mechanism independent of hypoxia-ischemia leading to metabolic acidosis.

IN other words, infection can cause significant morbidity in the absence of acidosis. Hence the need to not only think Cord Gases but also Infection when faced with a depressed newborn.

Art

At Sun, 9 Apr 2006, Grace Loehr wrote: >
>Robert Modugno:
>Just to be a devil's advocate. Why in the heck to we NEED to do
>cultures of the placenta. Don't we KNOW what organisms are involved in
>amniotic fluid infection? We usually give broad-spectrum antibiotic
>coverage. I don't see any reason to do it unless you are looking to
>document the more esoteric infections. Educate me!
>
>Please educate me as well. What organisms are usually responsible for
>placental infection? The mom is treated per symptoms before baby is
>born (hopefully), so of what use are the cultures? What do you all do
>with the lab results when you get them a few days later? Anything? Is
>there evidence based research for this practice? (I know, I know, you
>all are manly men of steel who don't need no stinkin' evidence. Just
>humor me, please.)
>
>Grace RN

--
art fougner, md
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