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三级医疗中心血红蛋白病患者的妊娠结局

Outcome of Pregnancy with Hemoglobinopathy in a Tertiary Care Center.

作者信息

Chauhan Anahita, Prasad Madhva

机构信息

Department of Gynecology and Obstetrics, Seth GS Medical College and KEM Hospital, Acharya Donde Marg, Parel, Mumbai, Maharashtra 400012 India.

出版信息

J Obstet Gynaecol India. 2018 Oct;68(5):394-399. doi: 10.1007/s13224-017-1073-5. Epub 2017 Nov 11.

DOI:10.1007/s13224-017-1073-5
PMID:30224845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6133791/
Abstract

PURPOSE

The objective was to observe the characteristics among pregnant patients with a diagnosed hemoglobinopathy and to study the obstetric and medical morbidity patterns during the antenatal and the perinatal periods in this group of patients.

METHODS

A prospective observational study was conducted in a tertiary care center.

RESULTS

Sixty patients were studied in 11 months. Primigravidae (43.3%) formed the highest percentage of patients. β Thalassemia trait was the most common hemoglobinopathy, seen in 81.66% of study subjects. The hemoglobin value ranged from 5.7 to 13.0, with an average of 9.2 g/dl. Thyroid problems were the most common associated medical disorder. Though IUGR and placenta previa were common, there were no major obstetric problems. There were 57 live births and 1 fresh stillbirth. Two patients had spontaneous abortion for which uterine curettage was done. LSCS was the most common obstetric outcome. Patients with sickle-cell disease required more blood transfusion than those with beta-thalassemia trait. There were 2 maternal mortalities, and both the patients were the diagnosed cases of sickle-cell disease.

CONCLUSIONS

While the perinatal outcomes among women with sickle-cell disease are poor, the outcomes in pregnant patients with beta-thalassemia trait were not a cause of major concern.

摘要

目的

观察确诊为血红蛋白病的孕妇的特征,并研究该组患者在产前和围产期的产科及内科发病模式。

方法

在一家三级医疗中心进行了一项前瞻性观察研究。

结果

在11个月内对60例患者进行了研究。初产妇(43.3%)占患者比例最高。β地中海贫血特征是最常见的血红蛋白病,在81.66%的研究对象中可见。血红蛋白值范围为5.7至13.0,平均为9.2g/dl。甲状腺问题是最常见的相关内科疾病。虽然胎儿生长受限和前置胎盘很常见,但没有重大产科问题。有57例活产和1例新鲜死产。2例患者发生自然流产并进行了刮宫术。剖宫产是最常见的产科结局。镰状细胞病患者比β地中海贫血特征患者需要更多输血。有2例孕产妇死亡,且这两名患者均为镰状细胞病确诊病例。

结论

虽然镰状细胞病女性的围产期结局较差,但β地中海贫血特征的孕妇结局并非主要担忧原因。

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Ann Hematol. 2017 Jun;96(6):1015-1021. doi: 10.1007/s00277-017-2979-9. Epub 2017 Mar 20.
2
Sickle cell disease and pregnancy outcomes: a study of the community-based hospital in a tribal block of Gujarat, India.镰状细胞病与妊娠结局:印度古吉拉特邦一个部落地区社区医院的研究
J Health Popul Nutr. 2017 Jan 21;36(1):3. doi: 10.1186/s41043-017-0079-z.
3
Prevalence of thalassemia and hemoglobinopathy in eastern India: A 10-year high-performance liquid chromatography study of 119,336 cases.印度东部地中海贫血和血红蛋白病的患病率:一项对119336例病例进行的为期10年的高效液相色谱研究。
Asian J Transfus Sci. 2016 Jan-Jun;10(1):105-10. doi: 10.4103/0973-6247.175424.
4
Pregnancy outcomes among women with beta-thalassemia trait.β地中海贫血特征女性的妊娠结局。
Arch Gynecol Obstet. 2016 Apr;293(4):771-4. doi: 10.1007/s00404-015-3908-6. Epub 2015 Oct 17.
5
Pregnancy outcomes among women with hemoglobin E trait.血红蛋白E性状女性的妊娠结局。
J Matern Fetal Neonatal Med. 2016;29(7):1146-8. doi: 10.3109/14767058.2015.1038515. Epub 2015 Apr 29.
6
[The pregnancy outcome in patients WITH β-thalassemia minor].[轻度β地中海贫血患者的妊娠结局]
Akush Ginekol (Sofiia). 2014;53 Suppl 1:20-4.
7
Pregnancy in beta-thalassemia intermedia: 20-year experience of a Greek thalassemia center.中间型β地中海贫血患者的妊娠:希腊地中海贫血中心20年经验
Eur J Haematol. 2014 Dec;93(6):492-9. doi: 10.1111/ejh.12387. Epub 2014 Jun 26.
8
Carrier Screening for β Thalassemia in Pregnant Indian Women: Experience at a Single Center in Madhya Pradesh.印度孕妇β地中海贫血的携带者筛查:中央邦一个单一中心的经验
Indian J Hematol Blood Transfus. 2013 Jun;29(2):71-4. doi: 10.1007/s12288-012-0165-8. Epub 2012 Jun 22.
9
Perinatal outcome in sickle cell anemia: a prospective study from India.镰状细胞贫血的围产期结局:一项来自印度的前瞻性研究。
Hemoglobin. 2013;37(6):507-15. doi: 10.3109/03630269.2013.828301. Epub 2013 Aug 19.
10
Pregnancy outcomes amongst thalassemia traits.地中海贫血症患者的妊娠结局。
Arch Gynecol Obstet. 2013 Nov;288(5):1051-4. doi: 10.1007/s00404-013-2886-9. Epub 2013 May 17.