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首页> 外文期刊>Journal of Patient-Reported Outcomes >Patients’ satisfaction with long-acting injectable somatostatin analog therapy for neuroendocrine tumors
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Patients’ satisfaction with long-acting injectable somatostatin analog therapy for neuroendocrine tumors

机译:患者对神经内分泌肿瘤的长效注射生长抑制素模拟疗法的满意度

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BackgroundLong-acting somatostatin analogs (LA SSAs) are approved and recommended for the treatment of patients with advanced neuroendocrine tumors (NETs). Given the long duration of therapy and differences in administration routes, it is important to understand patients’ experiences with receiving LA SSA injections.MethodsWe conducted a serial survey, informed by qualitative interviews with eight patients treated with LA SSAs and two nurses who administer LA SSA injections, among patients undergoing LA SSA treatment over a 28-day period (administered at baseline and 14?days and 28?days after injection). Eligible patients, recruited by the Carcinoid Cancer Foundation, self-reported having received an LA SSA injection for physician-diagnosed NET within the 5?days before the survey.Results202 patients completed the survey at baseline (82 receiving lanreotide and 120 receiving octreotide), 148 at day 14, and 124 at day 28. Patients reported consistently high satisfaction levels with their most recent LA SSA injection (91.1% at baseline, 85.1% at day 14, and 85.5% at day 28); 68.8% reported that their injection experience differed based on the nursing staff administering the injection.ConclusionsSatisfaction with LA SSA injections is high among patients in this population, and specific experiences with LA SSA injections varied based on the nursing staff administering the injection. Evaluations of patients’ experiences and satisfaction with treatment are increasingly important as patients take more active roles in decision-making for their treatment pathways.
机译:Backgroundlong作用生长抑素类似物(La SSA)被批准,并推荐用于治疗先进神经内分泌肿瘤(网)的患者。鉴于持续时间的治疗和行政路线的差异,了解患者与接受La SSA注射的患者的经验。近奇度调查进行了序列调查,通过定性访谈与八名患者治疗La SSA和管理La SSA的两名护士进行了通知在28天(在基线给药和14天和28天)进行La SSA治疗的患者中注射液中的注射剂。符合条件患者,由类癌癌症基础募集,自我报告的是在调查前5?日内接受了La SSA注射的ISA注射液,在调查前的时间内进行了诊断的网。患者在基线完成了调查(82升接受兰德雷德和120种接受octreotide接受八氧化物), 148天在第14天,第124天,第28天。患者报告始终如一的高度满意程度,最近的La SSA注射(91.1%在基线91.1%,第14天的85.1%和85.5%); 68.8%据报道,它们的注射经验基于给予注射的护理人员不同。与La SSA注射的联合疗法在该人群中的患者高,以及La SSA注射的特定经验根据管理注射的护理人员而变化。随着患者对其治疗途径的决策中更积极的作用,对治疗的评估越来越重要。

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