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首页> 外文期刊>Transplantation Proceedings >Conversion from mycophenolate mofetil to enteric-coated mycophenolate sodium in renal transplant recipients with gastrointestinal tract disorders.
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Conversion from mycophenolate mofetil to enteric-coated mycophenolate sodium in renal transplant recipients with gastrointestinal tract disorders.

机译:在患有胃肠道疾病的肾移植接受者中,从霉酚酸酯转化为肠溶性霉酚酸钠。

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OBJECTIVE: The objective of this prospective study was to evaluate the effect of conversion from mycophenolate mofetil (MMF) to enteric-coated mycophenolate sodium (EC-MPS) in renal transplant recipients with gastrointestinal tract (GI) reverse effects using patient-reported outcomes instrument. METHODS: A multicenter, open-label, prospective study was undertaken in renal transplant recipients treated with MMF. In patients experiencing GI tract symptoms, treatment was changed to equimolar EC-MPS (myfortic). At baseline and visit 2 (4-6 weeks after baseline), patients completed the Gastrointestinal Symptom Rating Scale (GSRS) and Gastrointestinal Quality of Life Index (GIQLI), and physicians completed the Overall Treatment Effect (OTE) scale at visit 2. A difference of 0.5 or greater in the OTE score is indicative of clinical relevance. RESULTS: Of 154 patients screened, 118 fulfilled the inclusion or exclusion criteria. Eighty-five men and 33 women with a mean age of 41.6 years participated in this study. Median time since transplantation was 12 months. Mean (SD) dose of MMF reported at baseline was 1209.4 (422.89) mg/d. More than 50% of patients reported MMF-associated nausea, dyspepsia, and abdominal pain. After conversion to an equimolar dose of EC-MPS, patients showed improvement in GI symptoms. This benefit was predominantly observed in patients with moderate to severe symptoms at baseline. On the GSRS, patients reported a significant (P < .05) reduction in symptom burden across all parameters (reflux, 36%; diarrhea, 38%; indigestion, 36%; constipation, 28%; and abdominal pain, 40%). On the GIQLI also, significant (P < .05) improvement was reported (symptoms, 18%; emotional status, 22%; physical functioning, 21%, and use of medical treatment, 18%). On the OTE scale, 84.7% of patients reported improvement in GI symptoms. CONCLUSION: In patients with moderate to severe GI symptoms, changing treatment from MMF to EC-MPS significantly reduces GI-related symptom burden and improves GI-specific quality of life.
机译:目的:这项前瞻性研究的目的是评估使用患者报告的结局仪器,从霉酚酸酯(MMF)转化为肠溶性霉酚酸钠(EC-MPS)对胃肠道(GI)不良反应的肾移植患者的影响。方法:对接受MMF治疗的肾移植接受者进行了一项多中心,开放性,前瞻性研究。对于出现胃肠道症状的患者,治疗方法改为等摩尔EC-MPS(霉菌性)。在基线和第2次就诊(基线后4-6周)时,患者完成了胃肠道症状评定量表(GSRS)和胃肠道生活质量指数(GIQLI),医生在第2次就诊时完成了总体治疗效果(OTE)量表。 OTE得分的差值大于或等于0.5表示临床相关。结果:在筛选的154例患者中,有118例符合纳入或排除标准。八十五名男性和三十三名女性,平均年龄为41.6岁,参加了这项研究。自移植以来的中位时间为12个月。基线时报告的MMF平均(SD)剂量为1209.4(422.89)mg / d。超过50%的患者报告有MMF相关的恶心,消化不良和腹痛。转换为等摩尔剂量的EC-MPS后,患者的胃肠道症状有所改善。主要在基线时出现中度至重度症状的患者中观察到这种益处。在GSRS上,患者报告所有参数的症状负担均显着降低(P <.05)(反流36%;腹泻38%;消化不良36%;便秘28%;腹痛40%)。在GIQLI上,也有显着(P <.05)改善(症状为18%;情绪状态为22%;身体机能为21%,药物治疗为18%)。在OTE量表上,有84.7%的患者报告了GI症状的改善。结论:对于中度至重度胃肠道症状的患者,将治疗从MMF改为EC-MPS可以显着减少与胃肠道相关的症状负担,并改善特定于胃肠道的生活质量。

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