The IMPACT Survey: the humanistic impact of osteogenesis imperfecta in adults

被引:0
|
作者
van Welzenis, Taco [1 ]
Westerheim, Ingunn [1 ]
Hart, Tracy [2 ]
Wekre, Lena Lande [3 ]
Semler, Oliver [4 ,5 ]
Rauch, Frank [6 ]
Dewavrin, Laetitia [7 ]
Dadzie, Ruby [7 ]
Prince, Samantha [7 ]
Raggio, Cathleen [8 ]
机构
[1] Osteogenesis Imperfecta Federat Europe, Heffen, Belgium
[2] Osteogenesis Imperfecta Fdn, Gaithersburg, MD USA
[3] Sunnaas Rehabil Hosp, TRS Natl Resource Ctr Rare Disorders, Nesodden, Norway
[4] Univ Cologne, Fac Med, Cologne, Germany
[5] Univ Cologne, Univ Hosp Cologne, Dept Pediat, Cologne, Germany
[6] McGill Univ, Montreal, PQ, Canada
[7] Wickenstones Ltd, Oxford, Oxon, England
[8] Hosp Special Surg, New York, NY USA
关键词
Osteogenesis imperfecta; Patient-reported outcomes; Survey; Burden of disease; Fractures; Humanistic burden; Quality of life; Health worries; Pain; Fatigue; Self-reported disease severity; QUALITY-OF-LIFE; PHYSICAL-DISABILITIES; PEOPLE; HEALTH; PAIN; LONELINESS; SATISFACTION; MANAGEMENT; FRACTURES; STOICISM;
D O I
10.1186/s12889-024-20555-0
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
BackgroundThe IMPACT Survey explored the humanistic, clinical, and economic burden of osteogenesis imperfecta (OI) on individuals with OI, their families, caregivers, and wider society. Two previous publications report research methodology, initial insights of the survey, and cost of illness of OI. Here, we present data on the impact of OI on the quality of life (QoL) of adults with OI and explore potential drivers of this impact.MethodsThe IMPACT Survey was an international mixed methods online survey in eight languages (fielded July-September 2021), aimed at adults (aged >= 18 years) or adolescents (aged 12-17 years) with OI, caregivers (with or without OI) of individuals with OI, and other close relatives. Survey domains included demographics, socioeconomic factors, clinical characteristics, treatment patterns, QoL, and health economics. We conducted a descriptive analysis of the QoL data, as well as exploratory regression analyses to identify drivers of impact of OI on QoL (independent associations between patient characteristics and the impact on QoL).Results1,440 adults with OI participated in the survey. The proportion who reported an impact of OI on their QoL across individual areas in the physical, socioeconomic, and mental well-being domains ranged between 49 and 84%. For instance, 84% of adults reported an impact of OI on the types of leisure activities they could do and 74% on the type of job they could do. More severe self-reported OI and higher fracture frequency were consistently identified as drivers of OI's impact on QoL. The proportion of adults who reported worrying about different aspects of their lives due to their OI, such as mobility loss, future fractures, and ageing, ranged between 31 and 97%.ConclusionIMPACT provides insights into the humanistic burden of OI on adults, revealing that OI has a substantial impact on the QoL of adults. OI severity and fracture frequency were consistently identified as drivers of impact on QoL across all domains. Understanding these drivers may aid in identifying areas for targeted interventions, such as fracture prevention.
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页数:13
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