通过强化循证、逐级培训模式提高加纳卫生工作者的能力,改善淋巴丝虫病 MMDP 服务的可及性:一项评估研究

C. Ahorlu, S. Atinbire, K. M. Sedzro, Bright Alomatu, Dziedzom K. de Souza, Kofi Asamenyi-Mensah, Joseph Opare, Paul Saunderson, Stefanie Weiland
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引用次数: 0

摘要

加纳在降低淋巴丝虫病的传播率方面取得了重大进展。然而,在提供发病率管理和残疾预防(MMDP)服务方面进展甚微,而这是证明消灭这种具有公共卫生重要性的疾病的关键要求之一。本研究旨在比较干预前和干预后,以确定加纳卫生工作者能力加强梯级培训模式的可行性和有效性,使用世卫组织推荐的最低干预一揽子计划来改善获得MMDP服务的机会。本研究采用准实验设计来评估加纳上西部地区淋巴丝虫病(LF)患者循证培训的影响。所有在数据收集时可用的淋巴水肿患者在训练前后都参加了研究。调查对象基线时平均年龄为54.67岁(SD±16.89岁),评估时平均年龄为54.70岁(SD±15.80岁)。调查对象中女性居多,基线时76.30%,评估时80.50%。大多数受访者未完成小学教育(基线时为83.82%,评估时为85.40%)。我们发现LF患者的生活质量有所改善,即报告生活质量高的受访者比例从基线时的2.9%增加到评估时的20.12% (p < 0.001)。73.17%的应答者在评估时报告了“卫生/患肢清洗和干燥”的淋巴水肿管理做法,而基线时只有32.95%的应答者报告了这一做法(p < 0.001)。采用“冷水/冷敷冷却患肢”的急性发作管理技术的受访者在评估时为70.15%,而基线时为23.70% (p < 0.001)。研究证实,社区成员在基线和评估时,与lf相关的认知基本保持不变。与基线相比,lf相关发病率管理(MMDP)项目的实施使评估患者的发病率管理实践有了显著改善。我们的研究结果还表明,自我护理可以改善患者的生活质量。这证明有必要投资于流行社区的发病率管理干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improving access to lymphatic filariasis MMDP services through an enhanced evidence-based, cascaded training model for health worker capacity strengthening in Ghana: an evaluation study
Ghana has made significant progress in reducing the transmission rate of lymphatic filariasis. However, very little progress has been made in the provision of morbidity management and disability prevention (MMDP) services, which is one of the key requirements for certification of elimination as a disease of public health importance. This study was designed to compare pre-post- intervention to determine the feasibility and effectiveness of a cascade training model for health worker capacity strengthening in Ghana, using the WHO recommended minimum intervention package to improve access to MMDP services.This study used a quasi-experimental design to assess the impact of evidence-based training of patients with lymphatic filariasis (LF) in the Upper West region of Ghana. All lymphedema patients who were available at the time of data collection participated in the study before and after the training.The mean age of respondents was 54.67 years (SD ± 16.89 years) at baseline and 54.70 years (SD ± 15.80 years) at evaluation. The majority (i.e., 76.30% at baseline and 80.50% at evaluation) of the respondents were female. Most of the respondents had not completed primary school (83.82% at baseline and 85.40% at evaluation). We found an improvement in the quality of life among LF patients, that is, the proportion of respondents who reported having a high quality of life increased from 2.9% at baseline to 20.12% at evaluation (p < 0.001). The lymphedema management practice of “hygiene/washing and drying of affected limb” was reported by 73.17% of respondents at evaluation compared with only 32.95% of respondents at baseline (p < 0.001). The acute attack management technique of “cooling the affected limb in cool water/cold compress” was reported by 70.15% of respondents at evaluation compared with 23.70% of respondents at baseline (p < 0.001).The research confirmed that LF-related perceptions remained generally the same at baseline and evaluation among community members. The implementation of the LF-related morbidity management (MMDP) project has led to a significant improvement in the morbidity management practices among patients at evaluation compared with baseline. Our findings also showed that self-care led to an improvement in patients’ quality of life. This justifies the need for investment in morbidity management interventions in endemic communities.
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