Management of anti-M antibody during pregnancy: a case report

被引:0
作者
Leibovitch, Emily R. [1 ,3 ]
Carlisle, Robert T. [2 ]
机构
[1] Univ Hawaii, John A Burns Sch Med, Honolulu, HI USA
[2] Univ Hawaii Manoa, John A Burns Sch Med, Dept Family Med, Honolulu, HI USA
[3] Univ Hawaii, John A Burns Sch Med, 651 Ilalo St, Honolulu, HI 96813 USA
关键词
antibodies; case reports; erythroblastosis; hydrops fetalis; pregnancy; prenatal care; ALLOIMMUNIZATION; ANEMIA;
D O I
10.1093/fampra/cmad067
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Anti-M antibodies are relatively common and naturally occurring. When anti-M antibodies cross the placenta, they may cause hemolytic disease of the fetus and newborn (HDFN). Anti-M antibodies account for less than 15 cases of HDFN reported in the published English literature. HDFN can lead to foetal anaemia, hydrops fetalis, hypoxia, heart failure, and even death. Objective To review the general guidelines and propose a less intensive management approach of anti-M antibody during pregnancy through the context of a case report. Methods We report a 25-year-old healthy pregnant G3P1011 woman presenting for antepartum care. At the time of delivery for the patient's second pregnancy, she was found to have a positive anti-M blood screen, though she birthed a healthy-term infant. For her current pregnancy, the initial and repeat testings for anti-M were positive. Results Since multiple samples from this patient were of low levels extensive maternal and foetal monitoring were deemed unnecessary in reflection of further reading and research. The patient had a spontaneous vaginal delivery of her third pregnancy at 38 weeks without complications. Conclusion Anti-RBC antibodies, including anti-M, are frequently identified in blood type and screening for pregnant patients. Guidelines call for intensive surveillance during pregnancy; however, knowledge of the specific antibody can help to provide more nuanced and less intensive care. As primary care physicians, being familiar with the guideline and the ability to counsel patients on anticipated care during pregnancy can help with family planning, compliance with testing, and patient anxiety and decrease intensive use of services that may not affect outcomes.
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共 14 条
[1]   Management of Alloimmunization During Pregnancy [J].
Holmgren, Calla ;
Porter, T. Flint .
OBSTETRICS AND GYNECOLOGY, 2018, 131 (03) :E82-E90
[2]  
Arora Satyam, 2015, Asian J Transfus Sci, V9, P98, DOI 10.4103/0973-6247.150968
[3]   Anti-M isoimmunization: Management and outcome at The Ohio State University from 1969 to 1995 [J].
DeYoungOwens, A ;
Kennedy, M ;
Rose, RL ;
Boyle, J ;
OShaughnessy, R .
OBSTETRICS AND GYNECOLOGY, 1997, 90 (06) :962-966
[4]   A single-center, retrospective analysis of 17 cases of hemolytic disease of the fetus and newborn caused by anti-M antibodies [J].
He, Yanjing ;
Gao, Wa ;
Li, Yang ;
Xu, Chang ;
Wang, Qiushi .
TRANSFUSION, 2023, 63 (03) :494-506
[5]   Risk of maternal alloimmunization in Southern Pakistan - A study in a cohort of 1000 pregnant women [J].
Karim, Farheen ;
Moiz, Bushra ;
Kamran, Nausheen .
TRANSFUSION AND APHERESIS SCIENCE, 2015, 52 (01) :99-102
[6]   Effect of screening for red cell antibodies, other than anti-D, to detect hemolytic disease of the fetus and newborn: a population study in the Netherlands [J].
Koelewijn, J. M. ;
Vrijkotte, T. G. M. ;
van der Schoot, C. E. ;
Bonsel, G. J. ;
de Haas, M. .
TRANSFUSION, 2008, 48 (05) :941-952
[7]   NEW CASES OF IRREGULAR BLOOD-GROUP ANTIBODIES OTHER THAN ANTI-D IN PREGNANCY - FREQUENCY AND CLINICAL-SIGNIFICANCE [J].
KORNSTAD, L .
ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 1983, 62 (05) :431-436
[8]   Distribution of maternal red cell antibodies and the risk of severe alloimmune haemolytic disease of the foetus in a Chinese population: a cohort study on prenatal management [J].
Li, Si ;
He, Zhiming ;
Luo, Yanmin ;
Ji, Yanli ;
Luo, Guangping ;
Fang, Qun ;
Gao, Yu .
BMC PREGNANCY AND CHILDBIRTH, 2020, 20 (01)
[9]   Fetal anemia due to non-Rhesus-D red-cell alloimmunization [J].
Moise, Kenneth J. .
SEMINARS IN FETAL & NEONATAL MEDICINE, 2008, 13 (04) :207-214
[10]  
Stetson B, 2017, AJP REP, V7, pE205, DOI 10.1055/s-0037-1607028