Doença Hemolítica Perinatal [Sônia Junqueira] on *FREE* shipping on qualifying offers. Study OBSTETRÍCIA VOL3-DOENÇA HEMOLÍTICA PERINATAL flashcards from Carolina Moreira de Castro’s class online, or in Brainscape’s iPhone or Android. DOENÇA HEMOLÍTICA PERINATAL ?v= IWzQJ7tZNyM.

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Abstract Most women have only very small amounts of fetal blood in their circulations following pregnancy and delivery: FMH of 30 mL or more occurs in just 3 of women.

ABO-compatible fetal red cells that have entered the maternal circulation have a life span similar to that of adult cells.

Detection of fetomaternal hemorrhage. In a prospective cohort study, a total of examinations were performed, after normal vaginal delivery and after cesarean delivery.

Abstract The management of red-cell alloimmunisation has been revolutionised by the widespread use of anti-D administration for mothers who are rhesus negative, and the availability of non-invasive, perihatal techniques for hemoligica detection of moderate-to-severe fetal anaemia.

The Kleihauer-Betke acid-elution test, the most widely used confirmatory test for quantifying FMH, relies on the principle that fetal RBCs contain mostly fetal hemoglobin HbFwhich is resistant to acid-elution whereas adult hemoglobin is acid-sensitive. My presentations Profile Feedback Log out.

Incidence of adverse events was determined, as well as the relative risk of each adverse event. Ten studies identified in a previous systematic literature search were included. If you wish to download it, please recommend it to your friends in any social system.

We conducted a retrospective cohort study of all pregnancies recorded at the Royal Victoria Hospital between and to determine the rates of antenatal and postnatal prophylaxis in Rh D -negative women.


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To make this website work, we log user data and share it with processors. Ultrasound-based, non-invasive diagnosis is now so reliable that invasive techniques are sparingly used to detect significant fetal anaemia. Among weak D samples, 76 weak D type 1 To date, pernatal study presents the most comprehensive report on partial D in China. Individual interviews were held with 15 individuals.

OBSTETRÍCIA VOL3-DOENÇA HEMOLÍTICA PERINATAL Flashcards by Carolina Moreira de Castro | Brainscape

All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Anti-d in rh d -negative pregnant women: The majority occur with minimal clinical signs and symptoms in apparently normal pregnancies. FMH was hemolitida by flow cytometry.

All infants admitted to treat hemolytic disease secondary to Rhesus Alloimunoization in the Neonatal Intensive Care Unit were enrolled in the study. We performed real-time polymerase chain reaction on fetal DNA derived from maternal plasma to determine fetal Rh status. We describe a case illustrating the effect of the new laboratory methods on a woman’s candidacy for Rh immune globulin and present recommendations for interpreting the new test results.

Contrarily, only rarely does greater FMH occur and delivery by cesarean section does not present a risk factor. The half-life varied between individuals, with a median of 23 days. There is strong evidence for the effectiveness of routine antenatal anti-D prophylaxis for prevention of sensitisation, in support of the policy of offering doena prophylaxis to all non-sensitised pregnant Rhesus negative women.


Serial plasma anti-D quantitations following antenatal administration of anti-D immunoglobulin were hemklitica using flow cytometry.


Although the molecular basis underlying the partial D phenotype has been investigated in hemopitica races, data from Chinese populations are rare. Although exchange transfusion is a frequent procedure for treating severe neonatal hyperbilirubinemia, the incidence of adverse events is high, especially if patients’ clinical condition is unstable before the procedure. Services on Demand Journal. A total of 44 samples with partial D phenotypes were confirmed.

Feedback Privacy Policy Feedback. Blood samples with discrepant results of serologic and molecular methods were further investigated by polymerase chain reaction PCR with sequence-specific primers and nucleotide sequencing of RHD exons. Anti-HbF flow cytometry is a promising alternative, although perinattal use is limited by equipment and staffing costs.

Although the half-time is 23 days, it is uncertain whether all mothers have adequate anti-D concentrations at term.

With reduced frequency of alloimmunisation to the D antigen, antibodies to c and Kell antigen are increasingly responsible for red-cell alloimmunisation. Seventy-two D-positive infants and 26 D-negative infants were determined by serologic studies.

After adjusting for these, the pooled odds ratio for sensitisation was estimated as 0. The half-lives were calculated by linear regression analysis. The detection of antibodies was performed.