Volume 10, Issue 1 (In Press 2022)                   J. Pediatr. Rev 2022, 10(1): 2-2 | Back to browse issues page


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Pahlevanynejad S, Danaei N, Kahouei M, Mirmohammadkhani M, Saffarieh E, Safdari R. Development and validation of the Iranian Neonatal Prematurity Minimum Data Set (IMSPIMDS): a systematic review, focus group discussion, and Delphi technique. J. Pediatr. Rev. 2022; 10 (1) :2-2
URL: http://jpr.mazums.ac.ir/article-1-413-en.html
1- Department of Health Information Management, School of Allied Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran.
2- Department of Pediatric, Semnan University of Medical Sciences, Semnan, Iran.
3- Department of Health Research Center, Semnan University of Medical Sciences, Semnan, Iran.
4- Department of Epidemiology and Biostatistics, Semnan University of Medical Sciences, Semnan, Iran.
5- Abnormal Uterine Bleeding Research Center, Semnan University of Medical Science, Semnan, Iran.
6- Department of Health Information Management, School of Allied Medical Sciences, Tehran University of Medical Sciences, Tehran, Iran. , rsafdari@tums.ac.ir
Abstract:   (724 Views)
Background: Information systems help to collect information about patients. The minimum data set (MDS) provides the basis for decision-making.
Objectives: This study was conducted to determine the comprehensive national MDS for prematurity information management system (IMSPIMDS) in Iran.
Methods: This research is a cross-sectional study with three steps including systematic review, focus group discussion, and Delphi technique. A systematic review was conducted in relevant databases. Then a focus group discussion was used to classify the extracted data elements by contributing specializing in various fields experts. Finally, MDSs were chosen through the decision Delphi technique in two rounds. Collected data were analyzed using IBM statistics SPSS 26.
Results: In total, 233 data elements were included in the Delphi survey. The data elements based on the experts’ opinions, were classified into two main categories including maternal and newborn. The final data elements categories were 107 and 126.
Conclusions: The existence of national MDS as the core of the premature newborn surveillance program is essential and leads to appropriate decisions. We developed and internally validated a minimum data set for prematurity researches. This study generated new knowledge to enable healthcare systems professionals to collect relevant and meaningful. The use of this standardized approach can help benchmark clinical practice and target improvements worldwide.
     
Type of Study: Systematic Review | Subject: Neonatology
Received: 2021/06/17 | Accepted: 2021/11/14 | Published: 2022/01/1

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