Baalmann Ann-Kristin, Blome Christine, Stoletzki Nina, Donhauser Theresa, Apfelbacher Christian, Piontek Katharina
Institute of Social Medicine and Health Systems Research, Faculty of Medicine, Otto von Guericke University, Magdeburg, Germany.
Institute for Health Services Research in Dermatology and Nursing (IVDP), University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.
BMJ Open. 2024 Dec 20;14(12):e084202. doi: 10.1136/bmjopen-2024-084202.
Post-COVID-19 condition (PCC), also referred to as Long COVID, has become an emerging public health issue requiring adequate prevention, treatment and management strategies. Evaluating these strategies from the patients' perspective using patient-reported outcome measures (PROMs) is critical. In this systematic review, we aimed to critically appraise and summarise the quality of existing PROMs for PCC, and to identify PROMs that can be recommended for use in future research.
Systematic review using the COnsensus-based Standards for the selection of health Measurement INstruments (COSMIN) methodology.
PubMed and Web of Science were searched on 16 January 2023 and again on 23 July 2024.
We included studies reporting on the development and/or validation of any disease-specific PROMs for PCC.
Two independent reviewers screened the results for eligibility. The methodological quality of each included study was assessed using the COSMIN Risk of Bias Checklist. We further evaluated the quality of measurement properties per PROM and study according to the criteria for good measurement properties as outlined in the COSMIN manual, and graded the evidence of the synthesised results. Based on the overall evidence, we derived recommendations for the use of the identified instruments.
We identified 23 studies reporting on 11 PROMs measuring functional status (COVID-19 Yorkshire Rehabilitation Scale, C19-YRS; Modified COVID-19 Yorkshire Rehabilitation Scale, C19-YRSm; Functional Impairment Checklist, FIC; Post-COVID-19 Functional Status Scale, PCFS), symptom burden and impact (Long COVID Symptom and Severity Score, LC-SSS; Long COVID Symptom Tool, LCST; Long COVID Impact Tool, LCIT; Symptom Burden Questionnaire Long COVID, SBQ-LC), quality of life (Post-acute COVID-19 Quality of Life instrument, PAC-19QoL) and stigma (Long COVID Stigma Scale, LCSS; Post-COVID-19 Condition Stigma Questionnaire, PCCSQ). Sample sizes of the included studies ranged from 29 to 1969 participants. Overall, 95 single studies on measurement properties were evaluated. Among the identified instruments, the Long Covid Stigma Scale (LCSS) showed sufficient content validity and internal consistency and can be recommended for use according to COSMIN criteria. Our assessment of measurement properties revealed significant evidence gaps for all PROMs, indicating the need for further validation studies to make an adequate decision on the recommendation for their use. Content validity is a major shortcoming of all included instruments.
The LCSS measuring stigma can be recommended for use in future research. For the assessment of PCC symptoms and impact, no instrument with sufficient measurement properties is currently available. Further validation of all identified PROMs is indicated, in particular comprehensive assessments of content validity involving experts and patients.
CRD42023391238.
新冠后状况(PCC),也被称为长新冠,已成为一个新出现的公共卫生问题,需要有适当的预防、治疗和管理策略。使用患者报告结局指标(PROMs)从患者角度评估这些策略至关重要。在这项系统评价中,我们旨在严格评估和总结现有用于PCC的PROMs的质量,并识别可推荐用于未来研究的PROMs。
采用基于共识的健康测量工具选择标准(COSMIN)方法进行系统评价。
于2023年1月16日以及2024年7月23日对PubMed和科学网进行检索。
我们纳入了报告任何针对PCC的特定疾病PROMs的开发和/或验证的研究。
两名独立的评审员筛选结果以确定其是否符合纳入标准。使用COSMIN偏倚风险清单评估每项纳入研究的方法学质量。我们还根据COSMIN手册中概述的良好测量属性标准,进一步评估每个PROM和研究的测量属性质量,并对综合结果的证据进行分级。基于总体证据,我们得出了关于所识别工具使用的建议。
我们识别出23项报告11种PROMs的研究,这些PROMs用于测量功能状态(新冠约克郡康复量表,C19 - YRS;改良新冠约克郡康复量表,C19 - YRSm;功能障碍清单,FIC;新冠后功能状态量表,PCFS)、症状负担及影响(长新冠症状与严重程度评分,LC - SSS;长新冠症状工具,LCST;长新冠影响工具,LCIT;症状负担问卷 - 长新冠,SBQ - LC)、生活质量(急性新冠后生活质量工具,PAC - 19QoL)和耻辱感(长新冠耻辱感量表,LCSS;新冠后状况耻辱感问卷,PCCSQ)。纳入研究的样本量从29名至1969名参与者不等。总体而言,共评估了95项关于测量属性的单项研究。在所识别的工具中,长新冠耻辱感量表(LCSS)显示出足够的内容效度和内部一致性,可根据COSMIN标准推荐使用。我们对测量属性的评估显示,所有PROMs都存在显著的证据缺口,这表明需要进一步的验证研究,以便就其使用建议做出充分的决策。内容效度是所有纳入工具的一个主要缺点。
可推荐长新冠耻辱感量表(LCSS)用于未来研究。对于PCC症状和影响的评估,目前尚无具有足够测量属性的工具。表明需要对所有识别出的PROMs进行进一步验证,特别是涉及专家和患者的内容效度综合评估。
PROSPERO注册号:CRD42023391238。