ArticlePerspectives in health information managemen2018
The Development of a Minimum Data Set for an Infertility Registry.
Article in Perspectives in health information managemen, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
12 citing papers in PubMed.
- Development of a minimum data set for a pediatric and neonatal Medication Administration Clinical Decision Support System (MACDSS), mapped to FHIR: a mixed-methods research synthesis.BMC medical informatics and decision making · 2026Article
- Primary Immunodeficiency Registry System: The Minimum Data Set Designing Phase-A Systematic Review and Quantitative Delphi Study.Health science reports · 2025Article
- Developing a minimum data set for the musculoskeletal physical therapy registry.Journal of education and health promotion · 2025Article
- Physical therapy registries worldwide: A systematic review.Health science reports · 2024Review
- Developing a minimum data set required to create a registry system for patients with vitiligo.Heliyon · 2022Article
- Internal validation and comparison of predictive models to determine success rate of infertility treatments: a retrospective study of 2485 cycles.Scientific reports · 2022Article
- A study to design minimum data set of COVID-19 registry system.BMC infectious diseases · 2021Article
- Developing the Minimum Dataset for the New Mexico Decedent Image Database.Applied clinical informatics · 2021Article
- Minimum Data Set for a Poisoning Registry: A Systematic Review.Iranian journal of pharmaceutical research : IJPR · 2021Review
- International Comparison of Thalassemia Registries: Challenges and Opportunities.Acta informatica medica : AIM : journal of the Society for Medical Informatics of Bosnia & Herzegovina : casopis Drustva za medicinsku informatiku BiH · 2019Article
- Development of a minimum data set for cardiac electrophysiology study ablation.Journal of education and health promotion · 2019Article
- The minimum data set for goiter disorder in Iran.Digital healthArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Effective decision making in the healthcare setting is highly dependent on access to reliable and robust data and information. A minimum data set is a standard assessment instrument that is used during the data collection process to ensure that decision makers have access to a consistent set of information. The objective of the current study was to develop a minimum data set for infertility patients that can be employed as the basis for an infertility registry in Iran. A systematic review resulted in the identification of 2,501 articles and 17 patient forms from infertility centers that were relevant to the study objectives. Of these, 10 articles met all the inclusion and exclusion criteria, and 232 data elements were subsequently extracted from these papers. The data elements were classified by three experts and validated via two rounds of a Delphi technique. The accessibility of the data elements was then evaluated during a focus group discussion. Finally, 146 data elements were selected as the minimum data set. The proposed minimum data set could provide the basis for standardization of infertility treatments. Synchronizing the various data sets that are currently in use will be necessary to allow sharing of data across infertility registries.
Indexed as
Identifiers
29618958PMC5869439What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.