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泛非肺动脉高压队列(PAPUCO)研究的原理与设计:在非洲实施一项关于肺动脉高压的当代注册研究。

Rationale and design of the Pan African Pulmonary hypertension Cohort (PAPUCO) study: implementing a contemporary registry on pulmonary hypertension in Africa.

作者信息

Thienemann Friedrich, Dzudie Anastase, Mocumbi Ana O, Blauwet Lori, Sani Mahmoud U, Karaye Kamilu M, Ogah Okechukwu S, Mbanze Irina, Mbakwem Amam, Udo Patience, Tibazarwa Kemi, Ibrahim Ahmed S, Burton Rosie, Damasceno Albertino, Stewart Simon, Sliwa Karen

机构信息

Clinical Infectious Diseases Research Initiative, Institute of Infectious Diseases and Molecular Medicine, Faculty of Health Science, University of Cape Town, Cape Town, South Africa.

Integerafrica Research & Development, Cape Town, South Africa.

出版信息

BMJ Open. 2014 Oct 14;4(10):e005950. doi: 10.1136/bmjopen-2014-005950.

Abstract

INTRODUCTION

Pulmonary hypertension (PH) is a devastating, progressive disease with increasingly debilitating symptoms and usually shortened overall life expectancy due to a narrowing of the pulmonary vasculature and consecutive right heart failure. Little is known about PH in Africa, but limited reports suggest that PH is more prevalent in Africa compared with developed countries due to the high prevalence of risk factors in the region.

METHODS AND ANALYSIS

A multinational multicentre registry-type cohort study was established and tailored to resource-constraint settings to describe disease presentation, disease severity and aetiologies of PH, comorbidities, diagnostic and therapeutic management, and the natural course of PH in Africa. PH will be diagnosed by specialist cardiologists using echocardiography (right ventricular systolic pressure >35 mm Hg, absence of pulmonary stenosis and acute right heart failure), usually accompanied by shortness of breath, fatigue, peripheral oedema and other cardiovascular symptoms, ECG and chest X-ray changes in keeping with PH as per guidelines (European Society of Cardiology and European Respiratory Society (ESC/ERS) guidelines). Additional investigations such as a CT scan, a ventilation/perfusion scan or right heart catheterisation will be performed at the discretion of the treating physician. Functional tests include a 6 min walk test and the Karnofsky Performance Score. The WHO classification system for PH will be applied to describe the different aetiologies of PH. Several substudies have been implemented within the registry to investigate specific types of PH and their outcome at up to 24 months. Data will be analysed by an independent institution following a data analyse plan.

ETHICS AND DISSEMINATION

All local ethics committees of the participating centres approved the protocol. The data will be disseminated through peer-reviewed journals at national and international conferences and public events at local care providers.

摘要

引言

肺动脉高压(PH)是一种具有毁灭性的进行性疾病,症状日益使人衰弱,由于肺血管变窄及随之而来的右心衰竭,总体预期寿命通常缩短。在非洲,人们对PH了解甚少,但有限的报告表明,由于该地区危险因素的高患病率,与发达国家相比,PH在非洲更为普遍。

方法与分析

建立了一项多国多中心登记型队列研究,并针对资源受限环境进行了调整,以描述非洲PH的疾病表现、疾病严重程度、病因、合并症、诊断和治疗管理以及自然病程。PH将由专科心脏病专家使用超声心动图(右心室收缩压>35 mmHg,无肺动脉狭窄和急性右心衰竭)进行诊断,通常伴有呼吸急促、疲劳、外周水肿和其他心血管症状,心电图和胸部X线变化符合指南(欧洲心脏病学会和欧洲呼吸学会(ESC/ERS)指南)中PH的表现。治疗医生可酌情进行其他检查,如CT扫描、通气/灌注扫描或右心导管检查。功能测试包括6分钟步行试验和卡诺夫斯基功能状态评分。将应用WHO的PH分类系统来描述PH的不同病因。在该登记研究中已开展了多项子研究,以调查特定类型的PH及其长达24个月的预后。数据将由一个独立机构按照数据分析计划进行分析。

伦理与传播

参与中心的所有当地伦理委员会均批准了该方案。数据将通过同行评审期刊、在国家和国际会议上以及在当地医疗服务提供者举办的公共活动中进行传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d352/4202005/5fc12555d2d0/bmjopen2014005950f01.jpg

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