9 Fertility, pregnancy and the management of myeloproliferative disorders

MD Martin Griesshammer (Head, Laboratory of Research on Haemostasis), MD Lothar Bergmann (Professor of Haematology), MD, FRCPath Tom Pearson (Professor of Haematology)
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引用次数: 49

Abstract

The management of pregnant patients with chronic myeloproliferative disorders (MPD) is a difficult problem. Patients with essential thrombocythaemia (ET), and, less frequently, those with chronic myeloid leukaemia (CML) or polycythaemia vera (PV), present at a childbearing age. Pregnancy itself does not appear to affect adversely the natural course and prognosis of the MPD. However, fertility might be reduced, and an adverse outcome of pregnancy due to thrombotic or bleeding complications is a matter of concern. In ET, first-trimester abortion is the most frequent complication but increased perinatal mortality and premature delivery are also observed. Placental infarction due to thrombosis seems to be the most consistent event. Maternal thrombotic or haemorrhagic complications are rare but are more common than seen in normal pregnancy. The outcome of pregnancy seems to be positively influenced by aspirin, at least in some cases. The value of cytoreduction and/or heparin prophylaxis has not been established but may have a role in selected cases. In CML, the potential adverse effects of hyperleukocytosis, and sometimes thrombocytosis, generally make myelosuppressive treatment essential. In PV, the number of reported pregnancies is low. Maintaining the PCV below 0.45 is of the utmost importance relating to the outcome of pregnancy. Although cytoreductive drugs should generally be avoided, if possible, until at least after the first trimester of pregnancy, interferon-α seems to be the drug of choice when myelosuppression is indicated.

In summary, the available information about pregnancy occurring during the course of an MPD indicates that successful management of pregnancy is possible. However, optimal management of these patients is poorly defined and agreed protocols are not available. In view of these problems, it is timely to consider the establishment of a national or European registry to monitor prospectively the management offered to pregnant women found to have an MPD.

生育、妊娠和骨髓增生性疾病的管理
慢性骨髓增生性疾病(MPD)孕妇的管理是一个难题。育龄期原发性血小板血症(ET)患者,以及较少见的慢性髓性白血病(CML)或真性红细胞血症(PV)患者。妊娠本身似乎不会对MPD的自然病程和预后产生不利影响。然而,生育能力可能会降低,并且由于血栓或出血并发症导致的妊娠不良后果是一个值得关注的问题。在ET中,妊娠早期流产是最常见的并发症,但也观察到围产期死亡率和早产的增加。由血栓形成引起的胎盘梗死似乎是最一致的事件。母体血栓形成或出血性并发症是罕见的,但比正常妊娠更常见。至少在某些情况下,阿司匹林对妊娠结局似乎有积极影响。细胞减少和/或肝素预防的价值尚未确定,但可能在选定的病例中起作用。在CML中,白细胞增多和血小板增多的潜在不良反应通常使骨髓抑制治疗必不可少。在PV,报告的怀孕数量很低。将PCV维持在0.45以下对妊娠结局至关重要。虽然细胞减少药物通常应该避免,如果可能的话,至少在怀孕的前三个月之后,干扰素-α似乎是首选的药物,当骨髓抑制是指。总之,关于MPD期间发生的妊娠的现有信息表明,成功的妊娠管理是可能的。然而,对这些患者的最佳管理没有明确的定义,也没有一致同意的方案。鉴于这些问题,考虑建立一个国家或欧洲的登记处,以前瞻性地监测对发现患有MPD的孕妇提供的管理是及时的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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