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Mass Screening

Clinical Research · NLM MeSH · updated 2026-10-29 · version 1

Citations verified against PubMedNot yet clinician-reviewed9 referencesApproximately 4 min read

Organized periodic procedures performed on large groups of people for the purpose of detecting disease.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 3 complete abstracts (793 words), 9 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

Organized periodic procedures performed on large groups of people for the purpose of detecting disease.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Mass Screenings; Screening, Mass; Screenings, Mass; Screening; Screenings.

Where it fits in the MeSH classification

Broader topics
Diagnostic Techniques and Procedures; Health Surveys; Diagnostic Services; Public Health Practice
Narrower topics
Anonymous Testing; Mass Chest X-Ray; Multiphasic Screening; Neonatal Screening; Pooled Testing; Vision Screening; Mandatory Testing; Substance Abuse Detection
See also
Sensitivity and Specificity

Research landscape

PubMed indexes 157,916 records tagged with the MeSH heading “Mass Screening” (counts retrieved 2026-10-29). 30,064 of them (19.0%) were published from 2020 onward, and the busiest period so far is 2010-2019 with 48,401 records.

Reviews account for 22,040 records (14.0%) and meta-analyses for 1,105. Randomized controlled trials number 4,187 (2.7%) as a share of all records on the topic.

PubMed records by publication periodthrough 1999: 39,556 records; 2000-2009: 39,895 records; 2010-2019: 48,401 records; 2020 onward: 30,064 records39,556through 199939,8952000-200948,4012010-201930,0642020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 199939,556
2000-200939,895
2010-201948,401
2020 onward30,064
Share of records by publication typeReviews: 14.0 percent; Meta-analyses: 0.7 percent; Randomized controlled trials: 2.7 percentReviews14.0% (22,040)Meta-analyses0.7% (1,105)Randomized controlled trials2.7% (4,187)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 157,916 PubMed records
TypeRecordsShare
Reviews22,04014.0%
Meta-analyses1,1050.7%
Randomized controlled trials4,1872.7%

Method: PubMed query "Mass Screening"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-29.

Reading the evidence in clinical research

Research methods determine how much a result can be trusted. Randomized trials guard against confounding, systematic reviews and meta-analyses combine many studies, and observational designs are valuable but can show only association. Reporting standards, trial registration and pre-specified outcomes reduce bias. When reading about a method, ask what problem it is designed to solve and which problems it does not solve.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Implementing a Risk-Stratified National Breast Screening Programme in the United Kingdom: A Model-Based Cost-effectiveness Analysis
Wright SJ, Hilton J, Rogers G, Gray E, Donten A, McWilliams L, et al.
2026Research article
Design not recorded in structured metadata
3cc by
PMID 42536349 · DOI · PMC13628088
Screen-Detected Coeliac Disease in a Nationally Representative Cohort: Health Indicators, Long-Term Outcomes and Mortality
Ahonen I, Kurppa K, Huhtala H, Kaukinen K, Kivelä L, Taavela J
2026Research article
Design not recorded in structured metadata
1cc by
PMID 42573482 · DOI · PMC13651919
Risk-Guided Screening for Atrial Fibrillation Using Electronic Health Records
Nadarajah R, Wu J, Wahab A, Reynolds C, Haris M, Joseph T, et al.
2026Research article
Design not recorded in structured metadata
1cc by
PMID 42517218 · DOI · PMC13506190

Implementing a Risk-Stratified National Breast Screening Programme in the United Kingdom: A Model-Based Cost-effectiveness Analysis [1]

Research article Wright SJ, Hilton J, Rogers G, Gray E, Donten A, McWilliams L, et al. · · 2026 · cited 3 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundRisk-stratified breast screening, in which women are offered different screening intervals based on their breast cancer risk, has been proposed as a way to improve the benefits of screening in the United Kingdom National Breast Screening Programme (UK-NBSP).
Closing excerpt
ImpactImplementation of risk-stratified breast screening in the UK national screening program has the potential to improve cancer detection at a reasonable additional resource use and cost.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (248 words)

BackgroundRisk-stratified breast screening, in which women are offered different screening intervals based on their breast cancer risk, has been proposed as a way to improve the benefits of screening in the United Kingdom National Breast Screening Programme (UK-NBSP). The aim of this study was to explore the cost-effectiveness of potential risk-stratified breast screening strategies in the UK-NBSP.MethodsAn existing validated discrete event simulation model (MANC-RISK-SCREEN) was used to evaluate the cost-effectiveness of 3 risk-stratified NBSPs (risk 1, risk 2, and risk 3) compared with the current UK-NBSP, 2-yearly screening, and no screening [lifetime horizon; health service perspective; costs (£; at 2024 prices)]. MANC-RISK-SCREEN was modified to account for bias in risk prediction and allocation to risk categories (risk misclassification). Uncertainty in the results due to model inputs was quantified using probabilistic sensitivity analysis and one-way sensitivity analyses.ResultsAt a cost-effectiveness threshold of £20,000 per quality-adjusted life year, 2-yearly screening was most likely to be cost-effective, followed by a risk-stratified approach whereby women at high risk (>8% 10-year risk) were screened annually and women at moderate risk (5%-8% 10-year risk) biannually. When risk misclassification was accounted for, the ranking of risk-stratified screening strategies improved relative to universal strategies.ConclusionsIf 2-yearly screening is infeasible due to resource constraints, implementing a risk-stratified approach in the existing NBSP in the United Kingdom would be a cost-effective use of healthcare resources.ImpactImplementation of risk-stratified breast screening in the UK national screening program has the potential to improve cancer detection at a reasonable additional resource use and cost.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42536349 · DOI · PMC13628088

Screen-Detected Coeliac Disease in a Nationally Representative Cohort: Health Indicators, Long-Term Outcomes and Mortality [2]

Research article Ahonen I, Kurppa K, Huhtala H, Kaukinen K, Kivelä L, Taavela J · · 2026 · cited 1 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundPopulation-based screening for coeliac disease could reduce underdiagnosis, but benefits and harms remain debated.
Closing excerpt
The results suggest a favourable benefit-harm balance for population-based screening.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (188 words)

BackgroundPopulation-based screening for coeliac disease could reduce underdiagnosis, but benefits and harms remain debated.AimWe studied health outcomes in screen-detected coeliac disease patients at diagnosis and following a long-term gluten-free diet.MethodsData were collected from Health 2000 and 2011 studies representing the Finnish population. Coeliac disease was screened in 6339 individuals by transglutaminase and endomysial antibodies, with dual seropositivity as the diagnostic criterion, histologically validated in this cohort. Survey-weighted analyses enabled population-level results. The follow-up cohort comprised those participating in both time points. Mortality was assessed between 2000 and 2017.ResultsAt screening, 92 (1.5%) undiagnosed coeliac disease patients and 6216 non-coeliac controls were identified. Patients were less often smokers (11% vs. 22%, p = 0.014), more often had a history of pre-eclampsia (13% vs. 5%, p = 0.037) and anaemia (14% vs. 6%, p = 0.012), and lower ferritin (29 vs. 68 ng/mL, p ConclusionsNationally screened adults with undiagnosed coeliac disease showed iron deficiency and anaemia. Long-term dietary treatment did not adversely affect quality of life or cardiometabolic health and may prevent complications. Furthermore, mortality was comparable to the general population. The results suggest a favourable benefit-harm balance for population-based screening.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42573482 · DOI · PMC13651919

Risk-Guided Screening for Atrial Fibrillation Using Electronic Health Records [3]

Research article Nadarajah R, Wu J, Wahab A, Reynolds C, Haris M, Joseph T, et al. · · 2026 · cited 1 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
BackgroundScreening for atrial fibrillation (AF) on the basis of AF risk may be more effective.
Closing excerpt
0, identifies a high-risk subpopulation for AF diagnosis among patients at elevated risk of stroke and could enable scalable, EHR-driven, risk-guided AF screening.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (357 words)

BackgroundScreening for atrial fibrillation (AF) on the basis of AF risk may be more effective. We aimed to develop, externally validate, and prospectively test a machine learning prediction model using electronic health records (EHRs) to guide AF screening.MethodsWe developed and validated a random forest prediction model for new AF within 6 months, using age, sex, and 10 comorbidities (Future Innovations in Novel Detection of Atrial Fibrillation [FIND-AF] 2.0) in EHRs in the United Kingdom (n=2 081 139), Japan (n=7 795 244), Israel (n=2 166 795), Canada (n=627 919), and China (n=149 145). We conducted a prospective study where participants ≥30 years old without AF and with a CHA2DS2-VASc score ≥2 in men and ≥3 in women, stratified by FIND-AF 2.0 into high and low risk, undertook 4 ECG recordings per day for 3 weeks using a handheld ECG recorder, with a primary outcome of newly diagnosed AF. We estimated stroke risk associated with nonanticoagulated AF in patients with high FIND-AF 2.0 risk in the FinACAF (Finnish Anticoagulation in Atrial Fibrillation) registry of patients with AF (n=229 565).ResultsFIND-AF 2.0 was applicable to all EHRs and showed good to excellent prediction performance (United Kingdom: area under the receiver operating characteristic curve [AUROC], 0.819 [95% CI, 0.809-0.829]; Israel: AUROC, 0.835 [95% CI, 0.828-0.842]; Japan: AUROC, 0.751 [95% CI, 0.745-0.757]; Canada: AUROC, 0.747 [95% CI, 0.741-0.753]; China: AUROC, 0.753 [95% CI, 0.725-0.771]), with AUROC>0.7 in men and women in all cohorts, and improved performance compared with CHA2DS2-VASc and C2HEST (coronary artery disease or chronic obstructive pulmonary disease [1 point each]; hypertension [1 point]; elderly [age ≥75 years, 2 points]; systolic HF [2 points]; thyroid disease [hyperthyroidism, 1 point]). Of 1923 participants from 15 sites in the prospective study (mean age, 70.2 [SD 9.4] years), with a mean of 74.8 (SD, 19.4) ECG recordings, AF was diagnosed in 5 of 902 (0.6%) with low FIND-AF 2.0 risk and 46 of 1021 (4.5%) with high FIND-AF 2.0 risk (odds ratio, 8.46 [95% CI, 3.35-21.40], PConclusionsThe EHR-based machine learning model, FIND-AF 2.0, identifies a high-risk subpopulation for AF diagnosis among patients at elevated risk of stroke and could enable scalable, EHR-driven, risk-guided AF screening.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42517218 · DOI · PMC13506190

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Accuracy of Patient Health Questionnaire-9 (PHQ-9) for screening to detect major depression: individual participant data meta-analysis [4]
    Levis B, Benedetti A, Thombs BD, DEPRESsion Screening Data (DEPRESSD) Collaboration · BMJ · 2019 · cited 1,349 times (Europe PMC)
  • Research article The benefits and harms of breast cancer screening: an independent review [5]
    Independent UK Panel on Breast Cancer Screening · Lancet · 2012 · cited 990 times (Europe PMC)
  • Research article A re-examination of Montreal Cognitive Assessment (MoCA) cutoff scores [6]
    Carson N, Leach L, Murphy KJ · Int J Geriatr Psychiatry · 2018 · cited 696 times (Europe PMC)
  • Research article Detecting cervical precancer and reaching underscreened women by using HPV testing on self samples: updated meta-analyses [7]
    Arbyn M, Smith SB, Temin S, Sultana F, Castle P, Collaboration on Self-Sampling and HPV Testing · BMJ · 2018 · cited 650 times (Europe PMC)
  • Research article Cognitive Tests to Detect Dementia: A Systematic Review and Meta-analysis [8]
    Tsoi KK, Chan JY, Hirai HW, Wong SY, Kwok TC · JAMA Intern Med · 2015 · cited 620 times (Europe PMC)
  • Research article Prostate cancer screening with prostate-specific antigen (PSA) test: a systematic review and meta-analysis [9]
    Ilic D, Djulbegovic M, Jung JH, Hwang EC, Zhou Q, Cleves A, et al. · BMJ · 2018 · cited 445 times (Europe PMC)

References

  1. Wright SJ, Hilton J, Rogers G, Gray E, Donten A, McWilliams L, et al.. Implementing a Risk-Stratified National Breast Screening Programme in the United Kingdom: A Model-Based Cost-effectiveness Analysis. . 2026. PMID 42536349 · DOI · PMC13628088
  2. Ahonen I, Kurppa K, Huhtala H, Kaukinen K, Kivelä L, Taavela J. Screen-Detected Coeliac Disease in a Nationally Representative Cohort: Health Indicators, Long-Term Outcomes and Mortality. . 2026. PMID 42573482 · DOI · PMC13651919
  3. Nadarajah R, Wu J, Wahab A, Reynolds C, Haris M, Joseph T, et al.. Risk-Guided Screening for Atrial Fibrillation Using Electronic Health Records. . 2026. PMID 42517218 · DOI · PMC13506190
  4. Levis B, Benedetti A, Thombs BD, DEPRESsion Screening Data (DEPRESSD) Collaboration. Accuracy of Patient Health Questionnaire-9 (PHQ-9) for screening to detect major depression: individual participant data meta-analysis. BMJ. 2019. PMID 30967483 · DOI · PMC6454318
  5. Independent UK Panel on Breast Cancer Screening. The benefits and harms of breast cancer screening: an independent review. Lancet. 2012. PMID 23117178 · DOI
  6. Carson N, Leach L, Murphy KJ. A re-examination of Montreal Cognitive Assessment (MoCA) cutoff scores. Int J Geriatr Psychiatry. 2018. PMID 28731508 · DOI
  7. Arbyn M, Smith SB, Temin S, Sultana F, Castle P, Collaboration on Self-Sampling and HPV Testing. Detecting cervical precancer and reaching underscreened women by using HPV testing on self samples: updated meta-analyses. BMJ. 2018. PMID 30518635 · DOI · PMC6278587
  8. Tsoi KK, Chan JY, Hirai HW, Wong SY, Kwok TC. Cognitive Tests to Detect Dementia: A Systematic Review and Meta-analysis. JAMA Intern Med. 2015. PMID 26052687 · DOI
  9. Ilic D, Djulbegovic M, Jung JH, Hwang EC, Zhou Q, Cleves A, et al.. Prostate cancer screening with prostate-specific antigen (PSA) test: a systematic review and meta-analysis. BMJ. 2018. PMID 30185521 · DOI · PMC6283370

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-29.

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At a glance

157,916
PubMed records on this heading
19%
published since 2020
22,040
review articles
4,187
randomized trials
9
verified references below

Counts come from PubMed on 2026-10-29; they show how much has been written, not how strong the evidence is.

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