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中华产科急救电子杂志 ›› 2016, Vol. 05 ›› Issue (02) : 97 -101. doi: 10.3877/cma.j.issn.2095-3259.2016.02.007

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妊娠合并溶血性贫血的诊断及治疗
黄婷婷1, 刘淮1,()   
  1. 1. 330006 南昌市,江西省妇幼保健院妇产科
  • 收稿日期:2016-02-09 出版日期:2016-05-18
  • 通信作者: 刘淮

Diagnosis and treatment of hemolytic anemia in pregnancy

Tingting Huang1, Huai Liu1()   

  • Received:2016-02-09 Published:2016-05-18
  • Corresponding author: Huai Liu
引用本文:

黄婷婷, 刘淮. 妊娠合并溶血性贫血的诊断及治疗[J]. 中华产科急救电子杂志, 2016, 05(02): 97-101.

Tingting Huang, Huai Liu. Diagnosis and treatment of hemolytic anemia in pregnancy[J]. Chinese Journal of Obstetric Emergency(Electronic Edition), 2016, 05(02): 97-101.

溶血性贫血是常见的遗传性疾病。随着医疗水平的提高,越来越多的妊娠合并溶血性贫血患者被发现。故如何高效地诊断并治疗此类患者,减少母婴并发症的发生是临床医生需要关注的重要问题。

Hemolytic anemia is the common genetic disease. With the improvement of medical treatment, more and more gravidas with hemolytic anemia are found. Therefore, clinician should pay attentions to how to effectively diagnose and treat the hemolytic anemia in pregnancy, which is in order to reduce the maternal and neonatal complications.

[1]
梁梅英,徐雪. 妊娠合并血液系统疾病孕期保健及诊治中应关注的问题[J/CD]. 中华产科急救电子杂志,2015, 4(1): 1-4.
[2]
Hanprasertpong T, Kor-anantakul O, Leetanaporn R, et al. Pregnancy outcomes amongst thalassemia traits[J]. Arch Gynecol Obstet, 2013, 288(5): 1051-1054.
[3]
Charoenboon C, Jatavan P, Traisrisilp K, et al. Pregnancy outcomes among women with beta-thalassemia trait[J]. Arch Gynecol Obstet, 2016, 293(4): 771-774.
[4]
Kolokairinou EM. The experience of beta-thalassaemiaand its prevention in Cyprus[J]. Med Law, 2008, 27(4): 825-841.
[5]
潘石蕾,黄郁馨. 妊娠合并地中海贫血[J/CD]. 中华产科急救电子杂志,2015, 4(1): 28-31.
[6]
王乐乐,刘慧姝. 妊娠合并地中海贫血[J]. 中国实用妇科与产科杂志,2015, 31(12): 1090-1095.
[7]
Ip HW, So CC. Diagnosis and prevention of thalassemia[J]. Crit Rev Clin Lab Sci, 2013, 50(6): 125-141.
[8]
Lam KW, Jiang P, Liao GJ, et al. Noninvasive prenataldiagnosis of monogenic diseases by targetedmassively parallel sequencing of maternal plasma:application to-β-thalassemia[J]. Clin Chem, 2012, 58(10): 1467-1475.
[9]
Diamantidis MD, Neokleous N, Agapidou A, et al. Iron chelation therapy of transfusion-dependent β-thalassemia during pregnancy in the era of novel drugs: is deferasirox toxic[J]. Int J Hematol, 2016, 103(5): 537-544.
[10]
Hannah Cohen, Hatrick O′Brien. Disorders of thrombosis and hemostasis in pregnancy[M]. 2nd ed. London: Springer International Publishing, 2015: 343-363.
[11]
Origa R, Piga A, Quarta G, et al. Pregnancy and beta-thalassemia thalassemia: an Italian multicenter experience[J]. Haematol, 2010, 95(3): 376-381.
[12]
Naik RP, Lanzkron S. Baby on board: what you need to know about pregnancy in the hemoglobinopathies[J]. Hematol Am Soc Hematol Educ Program, 2012, 2012: 208-214.
[13]
von Seidlein L, Auburn S, Espino F, et al.Review of key knowledge gaps in glucose-6-phosphate dehydrogenase deficiency detection with regard to the safe clinical deployment of 8-aminoquinoline treatment regimens: a workshop report[J]. Malar J, 2013, 12: 112.
[14]
胡玉婷,陈松长,罗玉琴,等. 罕见G6PD缺乏症合并21-三体综合征的分子遗传学研究[J]. 中国优生与遗传杂志,2014, 22(7): 9-11.
[15]
Joseph Rodgers, Hans-Peter Kohler. The biodemography of human reproduction and fertility[M]. New York: Springer US, 2003: 201-208.
[16]
Tsuzuki S, Akahira-Azuma M, Kaneshige M, et al. A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger[J]. Springerplus, 2013, 2: 434.
[17]
Christopher PC, Alfred PK, Ronald JS. Pediatric surgery[M]. Switzerland: Springer International Publishing, 2014: 293-297.
[18]
Allran CF, Weiss CA, Park AE. Urgent laparoscopic splenectomy in a morbidly obese pregnant woman: case report and literature review[J]. J Laparoendosc Adv Surg Tech A, 2002, 6(12): 446-447.
[19]
Hannah Cohen, Hatrick O′Brien. Disorders of thrombosis and hemostasis in pregnancy[M]. 2nd ed. London: Springer International Publishing, 2015: 327-342.
[20]
Fieni S, Bonfanti L, Gramellini D, et al. Clinical management of paroxysmal nocturnal hemoglobinuria in pregnancy: a case report and updated review[J]. Obstet Gynecol Surv, 2006, 61(9): 593-601.
[21]
Parker C, Omine M, Richards S, et al. Diagnosis and management of paroxysmal nocturnal hemoglobinuria[J]. Blood, 2005, 106(12): 3699-3709.
[22]
Allen TK, George RB, Olufolabi AJ, et al. The management of cesarean delivery in a parturient with paroxysmal nocturnal hemoglobinuria complicated by severe preeclampsia[J]. Can J Anaesth, 2007, 54(8):646-651.
[23]
Miyasaka N, Miura O, Kawaguchi T, et al. Pregnancy outcomes of patients with paroxysmal nocturnal hemoglobinuria treated with eculizumab: a Japanese experience and updated review[J]. Int J Hematol, 2016, 103(6): 703-712.
[24]
Jaime-Pérez JC, Rodríguez-Martínez M, Gómez-de-León A, et al. Current approaches for the treatment of autoimmune hemolytic anemia[J]. Arch Immunol Ther Exp (Warsz), 2013, 61(5): 385-395.
[25]
Genty I, Michel M, Hermine O, et al. Characteristics of autoimmune hemolytic anemia in adults: retrospective analysis of 83 cases[J]. Rev Med Interne, 2002, 23(11): 901-909.
[26]
Peter Valent, Klaus Lechner. Diagnosis and treatment of autoimmune haemolytic anaemias in adults: a clinical review[J]. Wien Klin Wochenschr, 2008, 120(5-6): 136-151.
[27]
Zanella A, Barcellini W. Treatment of autoimmune hemolytic anemias[J]. Haematologica, 2014, 99(10): 1547-1554.
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