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坦桑尼亚罕见病:国家行动呼吁,以解决罕见病患者的政策和紧急需求。

Rare diseases in Tanzania: a National Call for Action to address policy and urgent needs of individuals with rare diseases.

机构信息

Department of Haematology and Blood Transfusion, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Tanzania Human Genetics Organization, Dar es Salaam, Tanzania.

出版信息

Orphanet J Rare Dis. 2022 Sep 5;17(1):343. doi: 10.1186/s13023-022-02498-0.

Abstract

A rare disease is generally defined as a condition which affects about 1 among 2000 people and currently, there are approximately 5000-8000 rare diseases (RDs) affecting over 400 million people world-wide. Although RDs may arise from different causes such as infections and environmental factors, about 80% are caused by genetic abnormalities. In Tanzania, there are no reports of the types of RDs, their incidence, distribution and numbers of individuals affected. In addition, there have been no strategies to map RDs in the country and develop a definition that fits the local context. Public awareness and understanding of RDs are very limited, and these lead to poor management and stigmatisation of patients. To address the ongoing problems, Tanzania joined other countries world-wide and global partners to commemorate the rare diseases day (RDD) for the first time in 2016 and subsequently every year. Unlike previous years where the RDD was organised by Ali Kimara Rare Diseases Foundation (AKRDF) with few partners, in 2020, a bigger event was co-hosted by Ali AKRDF and Tanzania Human Genetics Organization together with government representatives and other multiple partners. The organisers, government representatives and participants proposed a national "Call for Action" with the overall goal of improving the lives of patients/individuals with RDs. The call focuses and aims to address 17 strategic issues that are broadly categorised into four areas. These include generating demographic data of individuals with RDs; advocating for policies and guidelines for diagnosis, care, treatment and health financing; developing policies supporting public education, awareness and advocacy; and strengthening research, innovation and public-private partnerships. If adopted and implemented, the potential impacts of these recommendations will include improved access to adequate and high-quality health and education services, and policies and guidelines to address the current and future challenges facing individuals with RDs and their families.

摘要

罕见病通常定义为影响每 2000 人中约 1 人的疾病,目前全世界约有 5000-8000 种罕见病(RDs)影响着超过 4 亿人。尽管 RDs 可能由感染和环境因素等不同原因引起,但约 80%是由遗传异常引起的。在坦桑尼亚,没有关于 RDs 类型、发病率、分布和受影响人数的报告。此外,该国也没有制定 RDs 图谱的战略,也没有制定适合当地情况的定义。公众对 RDs 的认识和理解非常有限,这导致患者的管理不善和受到歧视。为了解决这些持续存在的问题,坦桑尼亚与其他国家和全球合作伙伴一起,于 2016 年首次纪念罕见疾病日(RDD),随后每年都举行。与前几年由 Ali Kimara 罕见疾病基金会(AKRDF)与少数合作伙伴组织的 RDD 不同,2020 年,Ali AKRDF 和坦桑尼亚人类遗传学组织与政府代表和其他多个合作伙伴共同主办了一次更大的活动。组织者、政府代表和参与者提出了一项全国性的“行动呼吁”,其总体目标是改善 RDs 患者/个体的生活。该呼吁侧重于并旨在解决四大类共 17 个战略问题。这些问题包括收集 RDs 患者的人口数据;倡导诊断、护理、治疗和卫生筹资政策和指南;制定支持公众教育、宣传和倡导的政策;加强研究、创新和公私合作伙伴关系。如果这些建议得到采纳和实施,其潜在影响将包括改善获得充足和高质量的卫生和教育服务的机会,以及制定政策和指南,以应对 RDs 患者及其家庭目前和未来面临的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f07f/9446714/0bd16d2c0908/13023_2022_2498_Fig1_HTML.jpg

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