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一项关于两种针对性干预措施以提高成年血友病患者依从性的可行性研究。

A feasibility study on two tailored interventions to improve adherence in adults with haemophilia.

作者信息

Hoefnagels J W, Fischer K, Bos R A T, Driessens M H E, Meijer S L A, Schutgens R E G, Schrijvers L H

机构信息

Division Internal Medicine and Dermatology, Van Creveldkliniek, University Medical Center Utrecht, PO Box 85500, 3508, GA, Utrecht, The Netherlands.

Netherlands Haemophilia Patient Society (NVHP), Nijkerk, The Netherlands.

出版信息

Pilot Feasibility Stud. 2020 Dec 1;6(1):189. doi: 10.1186/s40814-020-00723-w.

Abstract

INTRODUCTION

Haemophilia is a congenital bleeding disorder mainly affecting males. To prevent bleeding, patients need to perform regular intravenous injections (prophylaxis) throughout life. Non-adherence often occurs. Problems with acceptance or self-management appear to be the main reasons for non-adherence in haemophilia. The aim of this study was to test the feasibility and effects of two interventions focussed on acceptance (face-to-face) and self-management (online).

METHODS

Patients with severe haemophilia and acceptance or self-management problems were eligible. The face-to-face group intervention was based on Acceptance and Commitment Therapy (ACT) (8 sessions/6 months, target N = 8 participants). The online intervention was based on a successful online programme in rheumatoid arthritis (5-8 modules/2 months, target N = 8). Both interventions were designed according to the MRC framework in collaboration with the patient society and experts. We compared adherence (VERITAS-Pro, optimum 0), quality of life (SF-36, optimum 100) and illness perception (BIPQ, optimum 0) before start (T0) and after 2 months (T2). Feasibility criteria were as follows: completion of training by > 50% of participants and ability to collect at least 80% of outcome parameters.

RESULTS

The face-to-face intervention was feasible (89% enrolment and recruitment, 100% retention). One hundred percent of the outcome parameters was collected. Results were promising: although adherence (VERITAS-Pro) was stable (from 64 to 62 points), quality of life (SF-36) showed a clinically relevant improvement (> 5 points) in five of eight domains. Illness perception (BIPQ) showed a clinically relevant increase from 47 to 39 points. Patient evaluation was positive. The online intervention, however, was infeasible: enrolment was only 20% (6/30). Only three patients signed informed consent (recruitment 10%), and none completed more than one module (retention 0%). Consequently, the online intervention was terminated.

CONCLUSION

The face-to-face acceptance intervention was considered feasible with promising results. Unfortunately, the online intervention was infeasible and therefore terminated. These findings suggest that adapting effective interventions to other settings does not guarantee success, despite the use of established methodology and patient participation. Population differences (only male participants, congenital disease) could be an explanation for failure of the online intervention in haemophilia despite success in rheumatoid arthritis.

TRIAL REGISTRATION

NL55883.041.16.

摘要

引言

血友病是一种主要影响男性的先天性出血性疾病。为预防出血,患者一生都需要定期进行静脉注射(预防治疗)。患者常常不坚持治疗。接受度或自我管理方面的问题似乎是血友病患者不坚持治疗的主要原因。本研究的目的是测试两种干预措施的可行性和效果,这两种干预措施分别侧重于接受度(面对面)和自我管理(在线)。

方法

患有重度血友病且存在接受度或自我管理问题的患者符合条件。面对面小组干预基于接受与承诺疗法(ACT)(8次 sessions/6个月,目标N = 8名参与者)。在线干预基于类风湿关节炎一项成功的在线项目(5 - 8个模块/2个月,目标N = 8)。两种干预措施均根据医学研究委员会(MRC)框架与患者协会和专家合作设计。我们比较了开始前(T0)和2个月后(T2)的依从性(VERITAS - Pro,最佳值0)、生活质量(SF - 36,最佳值100)和疾病认知(BIPQ,最佳值0)。可行性标准如下:超过50%的参与者完成培训,且能够收集至少80%的结局参数。

结果

面对面干预是可行的(89%的入组和招募率,100%的保留率)。收集到了100%的结局参数。结果很有希望:尽管依从性(VERITAS - Pro)稳定(从64分降至62分),但生活质量(SF - 36)在八个领域中的五个领域显示出临床相关改善(>5分)。疾病认知(BIPQ)从47分降至39分,显示出临床相关下降。患者评价为积极。然而,在线干预不可行:入组率仅为20%(6/30)。只有三名患者签署了知情同意书(招募率10%),且无人完成超过一个模块(保留率0%)。因此,在线干预终止。

结论

面对面接受度干预被认为是可行的,结果很有希望。不幸的是,在线干预不可行,因此终止。这些发现表明,尽管使用了既定方法和患者参与,但将有效干预措施应用于其他环境并不能保证成功。人群差异(仅男性参与者,先天性疾病)可能是在线干预在血友病中失败的原因,尽管在类风湿关节炎中取得了成功。

试验注册

NL55883.041.16

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aff3/7708110/63a695c89475/40814_2020_723_Fig1_HTML.jpg

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