Immune Thrombocytopenic Purpura in Pregnancy- A Prospective Observational Study in a Tertiary Care Centre

T. Parveen, F. Begum, N. Akhter, Nigar Sultana, K. Nahar
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Abstract

Objectives: Immune thrombocytopenic purpura (ITP) in pregnancy necessitates management of two patients, the mother and the newborn. Complications like maternal bleeding, fetal and neonatal thrombocytopenia demands appropriate and timely therapy. This prospective observational study was designed to explore and summarize the current approach to the investigation, diagnosis, management and outcome of ITP in pregnancy. Materials and Methods: Women with ITP admitted in the Fetomaternal Medicine Department of Bangabandhu Sheikh Mujib Medical University (BSMMU) from 2009 -2017, were included in the study. Total number of high risk pregnancy during that period were 7704 among them 20 cases were pregnancy with Immune Thrombocytopenic Purpura (ITP). Patients were managed under joint supervision of the fetomaternal medicine specialist and the hematologist. Prednisolone was considered as a first line drug in management protocol. Platelet transfusion was considered if there were symptoms or count <20X109/L at any stage of pregnancy or <50 X109 / L in late pregnancy without symptoms. Platelet count of newborn was performed at birth and repeated on day four and count<150X109/L was considered as neonatal thrombocytopenia. Results: Frequency of ITP among high risk patients was found 2.5/1000 live birth, most were preexisting (75%). Almost all cases (95%) were treated with prednisolone. Commonest clinical presentations were gum bleeding (70 %) and purpuric rashes (60%). Though during pregnancy, severe thrombocytopenia (<50 X109/L) was found in 7 patients (35%) but none was at the time of delivery, as drugs and/or platelet transfusion was considered to make delivery process safe. Platelet transfusion needed in 77.7% cases in a range of 1-75 units. Primary PPH noted in 3 cases (17%), increased bleeding during surgery in 5 patients (33%) and one patient needed ICU support. Neonatal thrombocytopenia noted in 5 cases (28%). Though 2 of the neonates needed NICU admission but none needed platelet transfusion and all the babies were discharged healthy. Conclusion: This study documents that pregnancy with ITP need close monitoring, require agents to raise the platelet count and repeated platelet transfusion to maintain reasonable safe platelet count. There are chances of PPH, capillary oozing during surgery. However good outcome is possible for most women, fetus and neonates with appropriate and timely therapy. Bangladesh J Obstet Gynaecol, 2019; Vol. 34(1): 15-21
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妊娠期免疫性血小板减少性紫癜——三级护理中心的前瞻性观察研究
目的:妊娠期免疫性血小板减少性紫癜(ITP)需要对母亲和新生儿两例患者进行治疗。并发症如产妇出血,胎儿和新生儿血小板减少症需要适当和及时的治疗。本前瞻性观察性研究旨在探讨和总结妊娠期ITP的调查、诊断、治疗和预后的现有方法。材料与方法:本研究纳入2009 -2017年Bangabandhu Sheikh Mujib医科大学(BSMMU)妇产科收治的ITP妇女。高危妊娠7704例,其中伴免疫性血小板减少性紫癜(ITP)妊娠20例。患者在妇产科专科医生和血液科医生的联合监督下进行管理。强的松龙被认为是治疗方案的一线药物。妊娠任一阶段有症状或血小板计数<20X109/L或妊娠晚期无症状血小板计数< 50x109 /L,可考虑输注血小板。新生儿出生时进行血小板计数,第4天重复计数,血小板计数<150 × 109/L为新生儿血小板减少症。结果:高危患者ITP发生率为2.5/1000例活产,多数为已存在(75%)。几乎所有病例(95%)都用强的松龙治疗。最常见的临床表现是牙龈出血(70%)和紫癜性皮疹(60%)。虽然在怀孕期间,7例(35%)患者发现严重的血小板减少(<50 X109/L),但在分娩时没有发生,因为药物和/或血小板输注被认为是安全的分娩过程。在1-75单位范围内,77.7%的病例需要输血小板。3例(17%)出现原发性PPH, 5例(33%)术中出血增加,1例需要ICU支持。新生儿血小板减少5例(28%)。2例新生儿需入新生儿重症监护病房,无一例需输血小板,出院时均健康。结论:本研究提示ITP妊娠需要密切监测,需要药物提高血小板计数,反复输血小板以维持合理安全的血小板计数。手术中有可能出现PPH,毛细血管渗出。然而,通过适当和及时的治疗,对大多数妇女、胎儿和新生儿来说,良好的结果是可能的。孟加拉国妇产科杂志,2019;Vol. 34(1): 15-21
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来源期刊
Bangladesh Journal of Obstetrics and Gynecology
Bangladesh Journal of Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
0.20
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发文量
16
期刊介绍: Bangladesh Journals OnLine (BanglaJOL) is a service to provide access to Bangladesh published research, and increase worldwide knowledge of indigenous scholarship
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