停止还是不停止:对机械通气的儿童骨髓和干细胞移植患者应给予多少支持?

Paul L Martin
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引用次数: 17

摘要

迄今为止,每一篇报道儿科SCT患者重症监护支持结果的出版物都必须谨慎阅读,因为它们都是单一机构的回顾性报告。然而,这些研究人员得出的一些结论似乎具有临床相关性。首先,需要重症监护支持的SCT患者的生存机会并不一定很渺茫。最近报道的存活率在15%到36%之间,当非icu患者的总体移植后存活率可能只有50%时,这是合理的。其次,不同中心的不良风险因素不同,可能是由于患者群体、供体来源和移植准备方案的广泛差异。第三,MSOF是一个持续的生存不利风险因素。从本文提供的数据中可以得出的另一个结论是,在PICU护理的第二周没有显着客观改善的患者不太可能存活。应向患者、患者家属和患者医生建议限制或撤销维持生命的医疗支持。虽然对于这些临床情况没有100%可靠的预测模型,但根据作者的经验,大多数家庭和医生认为在没有临床改善的情况下,超过2周的重症监护支持是徒劳的。很明显,我们需要前瞻性的、多机构的研究,包括干预措施的治疗效果,如高频振荡通气、持续静脉静脉血液透析、早期使用无创通气(即无创正压通气)、使用生物制剂减少炎症、新型抗真菌药物的影响,以及允许性高碳酸血症时的肺保护性通气。在这些潜在的治疗方法中,作者目前只知道一项涉及持续静脉静脉血液透析的多机构研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
To stop or not to stop: how much support should be provided to mechanically ventilated pediatric bone marrow and stem cell transplant patients?

Every publication to date reporting the outcome of intensive care support for pediatric SCT patients must be viewed with caution because all are single-institution, retrospective reports. Nevertheless, some of the conclusions made by these investigators appear to be clinically relevant. First, an SCT patient who requires intensive care support does not automatically have a dismal chance of survival. Survival rates in recent reports range from 15% to 36%, which is reasonable when the overall post-transplant survival rate for non-ICU patients may be only 50%. Second, adverse risk factors differ from center to center, likely due to the wide variation in patient populations, donor source, and transplant preparation regimens. Third, MSOF is a consistent adverse risk factor for survival. An additional conclusion that can be drawn from the data presented in this article is that patients who do not show significant, objective improvement by the second week of PICU care are unlikely to survive. The limitation or withdrawal of life-sustaining medical support should be recommended to the patient, the patient's family, and the patient's doctors. Although there are no predictive models that are 100% reliable for these clinical situations, in the author's experience, most families and physicians view critical care support beyond 2 weeks, in the absence of clinical improvement, as futile care. It is clear that better data are needed in the form of prospective, multi-institutional studies that include the therapeutic efficacy of interventions such as high-frequency oscillatory ventilation, continuous venovenous hemodialysis, early use of noninvasive ventilation (ie, noninvasive positive pressure ventilation), the use of biologic agents to decrease inflammation, the impact of new antifungal medications, and lung-protective ventilation with permissive hypercapnia. Of these potential therapies, the author is aware of only one multi-institutional study involving continuous venovenous hemodialysis at this time.

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