Tavakoli-Ardakani Maria, Kheshti Raziyeh, Maryam Mehrpooya
Department of Clinical Pharmacy, School of Pharmacy and Pharmaceutical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Clinical Pharmacy, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Int J Hematol. 2017 Dec;106(6):832-841. doi: 10.1007/s12185-017-2309-y. Epub 2017 Aug 16.
Previous studies have found a connection between psychiatric problems and post-hematopoietic stem-cell transplantation (HSCT) complications. We sought to evaluate the effect of sertraline on engraftment time, hospitalization period, mortality, and post-transplantation complications in HSCT recipients with depression and/or anxiety. We recruited adults aged 18-60, who were candidates for autologous or allogeneic HSCT with major depression and/or anxiety disorder. They were administered 50 mg of sertraline or placebo daily for the first week, and then 100 mg for the following seven weeks. We documented occurrence and severity of early post-HSCT complications, including infection, mucositis, nausea and vomiting, diarrhea, pain, renal toxicities and liver complications, acute graft-versus-host disease, and veno-occlusive disease, as well as time to engraftment, length of hospitalization and 6-month mortality. Overall, 56 patients participated in the study (sertraline group n = 30, placebo group n = 26). Of the complications, only mortality and readmission up to 6 months post-transplantation were significantly higher in the placebo group compared to sertraline group (P values = 0.040, 0.028, respectively). There were no significant differences for other complications between the groups. Mean engraftment time was significantly lower in the sertraline group (P value = 0.048). This study provides evidence that sertraline positively influences engraftment time, readmission, and mortality after HSCT.
先前的研究发现精神问题与造血干细胞移植(HSCT)后并发症之间存在关联。我们试图评估舍曲林对患有抑郁症和/或焦虑症的HSCT受者的植入时间、住院时间、死亡率及移植后并发症的影响。我们招募了18至60岁的成年人,他们是患有重度抑郁症和/或焦虑症的自体或异基因HSCT候选者。在第一周,他们每天服用50毫克舍曲林或安慰剂,接下来的七周每天服用100毫克。我们记录了HSCT后早期并发症的发生情况和严重程度,包括感染、粘膜炎、恶心和呕吐、腹泻、疼痛、肾毒性和肝脏并发症、急性移植物抗宿主病及静脉闭塞性疾病,以及植入时间、住院时长和6个月死亡率。总体而言,56名患者参与了该研究(舍曲林组n = 30,安慰剂组n = 26)。在并发症方面,与舍曲林组相比,安慰剂组仅移植后6个月内的死亡率和再次入院率显著更高(P值分别为0.040、0.028)。两组之间的其他并发症无显著差异。舍曲林组的平均植入时间显著更低(P值 = 0.048)。本研究提供了证据表明舍曲林对HSCT后的植入时间、再次入院率和死亡率有积极影响。