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Design and statistical analysis reporting among interrupted time series studies in drug utilization research: a cross-sectional survey.
Zhang, Yuanjin; Ren, Yan; Huang, Yunxiang; Yao, Minghong; Jia, Yulong; Wang, Yuning; Mei, Fan; Zou, Kang; Tan, Jing; Sun, Xin.
Afiliação
  • Zhang Y; Chinese Evidence-Based Medicine Center, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, 610041, Sichuan, China.
  • Ren Y; NMPA Key Laboratory for Real World Data Research and Evaluation in Hainan, Chengdu, China.
  • Huang Y; Sichuan Center of Technology Innovation for Real World Data, Chengdu, China.
  • Yao M; Hainan Healthcare Security Administration Key Laboratory for Real World Data Research, Chengdu, China.
  • Jia Y; Chinese Evidence-Based Medicine Center, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, 610041, Sichuan, China.
  • Wang Y; NMPA Key Laboratory for Real World Data Research and Evaluation in Hainan, Chengdu, China.
  • Mei F; Sichuan Center of Technology Innovation for Real World Data, Chengdu, China.
  • Zou K; Hainan Healthcare Security Administration Key Laboratory for Real World Data Research, Chengdu, China.
  • Tan J; Chinese Evidence-Based Medicine Center, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, 610041, Sichuan, China.
  • Sun X; NMPA Key Laboratory for Real World Data Research and Evaluation in Hainan, Chengdu, China.
BMC Med Res Methodol ; 24(1): 62, 2024 Mar 09.
Article em En | MEDLINE | ID: mdl-38461257
ABSTRACT

INTRODUCTION:

Interrupted time series (ITS) design is a commonly used method for evaluating large-scale interventions in clinical practice or public health. However, improperly using this method can lead to biased results.

OBJECTIVE:

To investigate design and statistical analysis characteristics of drug utilization studies using ITS design, and give recommendations for improvements.

METHODS:

A literature search was conducted based on PubMed from January 2021 to December 2021. We included original articles that used ITS design to investigate drug utilization without restriction on study population or outcome types. A structured, pilot-tested questionnaire was developed to extract information regarding study characteristics and details about design and statistical analysis.

RESULTS:

We included 153 eligible studies. Among those, 28.1% (43/153) clearly explained the rationale for using the ITS design and 13.7% (21/153) clarified the rationale of using the specified ITS model structure. One hundred and forty-nine studies used aggregated data to do ITS analysis, and 20.8% (31/149) clarified the rationale for the number of time points. The consideration of autocorrelation, non-stationary and seasonality was often lacking among those studies, and only 14 studies mentioned all of three methodological issues. Missing data was mentioned in 31 studies. Only 39.22% (60/153) reported the regression models, while 15 studies gave the incorrect interpretation of level change due to time parameterization. Time-varying participant characteristics were considered in 24 studies. In 97 studies containing hierarchical data, 23 studies clarified the heterogeneity among clusters and used statistical methods to address this issue.

CONCLUSION:

The quality of design and statistical analyses in ITS studies for drug utilization remains unsatisfactory. Three emerging methodological issues warranted particular attention, including incorrect interpretation of level change due to time parameterization, time-varying participant characteristics and hierarchical data analysis. We offered specific recommendations about the design, analysis and reporting of the ITS study.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Saúde Pública Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Saúde Pública Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article