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Infections

Infectious Diseases · NLM MeSH · updated 2026-10-29 · version 1

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

Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases.

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 (852 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

Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases.

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: Infection; Infection and Infestation; Infestation and Infection; Infections and Infestations; Infestations and Infections.

Where it fits in the MeSH classification

Narrower topics
Aneurysm, Infected; Arthritis, Infectious; Asymptomatic Infections; Bacterial Infections and Mycoses; Bone Diseases, Infectious; Breakthrough Infections; Cardiovascular Infections; Catheter-Related Infections; Central Nervous System Infections; Coinfection; Communicable Diseases; Community-Acquired Infections; Cross Infection; Eye Infections
See also
Anti-Infective Agents

Research landscape

PubMed indexes 3,396,820 records tagged with the MeSH heading “Infections” (counts retrieved 2026-10-29). 810,860 of them (23.9%) were published from 2020 onward, and the busiest period so far is through 1999 with 1,248,290 records.

Reviews account for 378,919 records (11.2%) and meta-analyses for 26,597. Randomized controlled trials number 65,106 (1.9%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.

PubMed records by publication periodthrough 1999: 1,248,290 records; 2000-2009: 563,494 records; 2010-2019: 774,176 records; 2020 onward: 810,860 records1,248,290through 1999563,4942000-2009774,1762010-2019810,8602020 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 19991,248,290
2000-2009563,494
2010-2019774,176
2020 onward810,860
Share of records by publication typeReviews: 11.2 percent; Meta-analyses: 0.8 percent; Randomized controlled trials: 1.9 percentReviews11.2% (378,919)Meta-analyses0.8% (26,597)Randomized controlled trials1.9% (65,106)
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 3,396,820 PubMed records
TypeRecordsShare
Reviews378,91911.2%
Meta-analyses26,5970.8%
Randomized controlled trials65,1061.9%

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

Reading the evidence in infectious diseases

Infectious disease evidence combines microbiology, epidemiology and clinical trials. Laboratory studies identify pathogens and how they cause harm; surveillance and outbreak investigations describe who is affected and how infection spreads; trials establish whether treatments and vaccines work. Results depend on place and time, because pathogens evolve and resistance patterns and population immunity change. Check when and where the data were collected, how cases were defined and how up to date the evidence is.

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
Temporal trends in incidence, clinical characteristics and outcomes of pyogenic vertebral osteomyelitis in Southern Denmark from 2009 to 2022: a retrospective population-based cohort study
Lindvig SO, Kehrer M, Petersen I, Hess S, Theilgaard ZP, Rosenvinge FS, et al.
2026Research article
Design not recorded in structured metadata
0cc by
PMID 42902785 · DOI · PMC13689801
Global mpox outbreak dynamics during and after the 2024-2026 public health emergency
Elvis Akem T
2026Research article
Design not recorded in structured metadata
0cc by
PMID 42905633 · DOI · PMC13686470
Applying normalized p-control charts for early detection of local COVID-19 outbreaks
Foox Y, Yamin D, Chalutz-BenGal H, Ben-Gal I
2026Research article
Design not recorded in structured metadata
0cc by
PMID 42900655 · DOI · PMC13682654

Temporal trends in incidence, clinical characteristics and outcomes of pyogenic vertebral osteomyelitis in Southern Denmark from 2009 to 2022: a retrospective population-based cohort study [1]

Research article Lindvig SO, Kehrer M, Petersen I, Hess S, Theilgaard ZP, Rosenvinge FS, et al. · · 2026

Abstract reading summary — source excerpts
Opening excerpt
ObjectivesPyogenic vertebral osteomyelitis (PVO) is a severe infection with increasing incidence.
Closing excerpt
Mortality remained high and increased over time.
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 (249 words)

ObjectivesPyogenic vertebral osteomyelitis (PVO) is a severe infection with increasing incidence. We aimed to describe long-term population-based temporal trends in incidence, clinical presentation, diagnostic approaches, microbiology, and outcomes.Materials and methodsWe conducted a retrospective population-based cohort study including 1,017 adults with multidisciplinary team-verified PVO diagnosed at a tertiary infectious diseases referral centre in the Region of Southern Denmark between 2009 and 2022. Incidence rates (IRs) per 100,000 person-years (PY) were calculated using regional population data and compared across three calendar periods (2009-2013, 2014-2018, 2019-2022). Temporal changes in clinical characteristics, microbiology, diagnostic strategies, and outcomes were assessed.ResultsIn total, 1,017 patients were included. The crude IR increased from 4.7 per 100,000 PY in 2009-2013 to 11.0 in 2019-2022, with the largest increase among patients aged ≥70 years. Mean age and comorbidity burden rose over time. Pain was common, fever was often absent, and neurological deficits occurred in 33.5% (n = 341). Postsurgical infection was the most frequent primary focus, and concomitant endocarditis occurred in 8.3% (n = 84). A microbiological diagnosis was established in 64.8% (n = 635) of cases, most commonly Staphylococcus aureus. Use of Fluorine-18 Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography ([18F]FDG-PET/CT) increased over time. Median hospital stay remained 33 days. One-year mortality increased from 9.5% to 18.2%, while relapse declined, resulting in a stable composite risk of death or relapse (20.7%).ConclusionsThe incidence of PVO increased markedly from 2009 to 2022, predominantly in older patients with comorbidities. Despite improved diagnostics, microbiologically-negative cases remain frequent. Mortality remained high and increased over time.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42902785 · DOI · PMC13689801

Global mpox outbreak dynamics during and after the 2024-2026 public health emergency [2]

Research article Elvis Akem T · · 2026

Abstract reading summary — source excerpts
Opening excerpt
The second WHO Public Health Emergency of International Concern (PHEIC) for mpox was declared on 14 August 2024 after clade Ib monkeypox virus emerged in the Democratic Republic of the Congo (DRC) and spread rapidly across Africa and internationally.
Closing excerpt
The post-emergency period requires sustained surveillance, maintained diagnostic capacity, targeted response in persistent transmission settings, and equitable access to vaccines and countermeasures.
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 (304 words)

The second WHO Public Health Emergency of International Concern (PHEIC) for mpox was declared on 14 August 2024 after clade Ib monkeypox virus emerged in the Democratic Republic of the Congo (DRC) and spread rapidly across Africa and internationally. The PHEIC ended on 5 September 2025, and the Africa CDC Public Health Emergency of Continental Security was lifted on 22 January 2026. This study characterised global and Africa-specific mpox epidemiology across the full second PHEIC cycle and immediate post-emergency period, from January 2024 to February 2026. A retrospective surveillance analysis was conducted using the WHO Global Mpox Trends dashboard exported data, supplemented by WHO situation reports S32-S64 and international and national surveillance reports. Analyses included negative binomial segmented regression, travel-linked pathway analysis, exploratory analysis of documented secondary transmission after travel-linked detection, and descriptive statistics. Models used reported case counts with log population offsets; reported case-rate ratios therefore reflect reported case rates rather than true infection incidence. Between January 2024 and February 2026, 82,738 confirmed cases and 306 deaths were reported to WHO globally (case fatality ratio 0.37%). The PHEIC period accounted for 74.0% of cases, peaking at 7,405 cases in May 2025. In total, 163 clade-specific importation or travel-linked detection events were documented across 41 countries within the primary analytic cutoff; documented secondary transmission occurred in 25 (15.3%) events across 16 countries. Within DRC, 200 health zones recorded 144,035 total reported cases and 2,047 deaths (case fatality ratio 1.42%); these aggregate suspected/clinically compatible and confirmed cases. The top 20 health zones accounted for 45.4% of national burden. Reported transmission declined after the May 2025 peak but persisted beyond PHEIC termination. Emergency termination marked an administrative transition, not the end of mpox transmission. The post-emergency period requires sustained surveillance, maintained diagnostic capacity, targeted response in persistent transmission settings, and equitable access to vaccines and countermeasures.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42905633 · DOI · PMC13686470

Applying normalized p-control charts for early detection of local COVID-19 outbreaks [3]

Research article Foox Y, Yamin D, Chalutz-BenGal H, Ben-Gal I · · 2026

Abstract reading summary — source excerpts
Opening excerpt
The COVID-19 pandemic underscored the urgent need for early detection of local outbreaks to enable better resource allocation and effective mitigation.
Closing excerpt
In the post-vaccination era, when targeted responses are key to controlling localized spread while avoiding widespread restrictions, health data analytics offer a valuable tool for informed decision-making.
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 (299 words)

The COVID-19 pandemic underscored the urgent need for early detection of local outbreaks to enable better resource allocation and effective mitigation. Outbreak identification largely depended on local infection rates, which were highly variable and influenced by daily testing volumes. Effective pandemic management requires accurate, adaptive methods that reflect the dynamic and localized nature of these rates, ensuring timely and appropriate interventions. This study seeks to improve the early detection and localization of COVID-19 outbreaks through Statistical Process Control (SPC) and health data analytics. We propose an adaptive outbreak-detection framework that combines a normalized p-control chart with an Amplitude-based labeler (ABL). For each area and day, the monitored statistic is a standardized positivity-rate score, computed from the observed daily positivity rate, the number of tests performed that day, and an area-specific baseline positivity estimate derived from recent historical observations. This calibration is followed by Phase II sequential monitoring using fixed three-sigma limits on the normalized scale and Western Electric decision rules. The framework accommodates varying daily sample sizes, captures regional interconnectedness, and supports parameter tuning using a temporally ordered train/test design. Accounting for daily testing fluctuations and spatial variability, it enhances the accuracy of local outbreak detection. Compared with the benchmark outbreak-detection methods considered in this study, the proposed framework was evaluated on its ability to predict outbreak onset within the following three days, achieving overall accuracy of 0.81 and averaged precision and recall of 0.83 and 0.79, respectively. Performance was further evaluated using the Fβ-measure, enabling a flexible trade-off between precision and recall depending on the relative cost of errors. SPC-based methods like ours can significantly improve early outbreak detection and localization. In the post-vaccination era, when targeted responses are key to controlling localized spread while avoiding widespread restrictions, health data analytics offer a valuable tool for informed decision-making.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 42900655 · DOI · PMC13682654

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 Burden and global distribution of antimicrobial resistance in non-bloodstream infections among adults with cirrhosis: A systematic review and proportional meta-analysis [4]
    Ozdemir C, Paul T, Egoh K, Wanford JJ, Dekker D, Shawcross DL, et al. · Int J Antimicrob Agents · 2026 · cited 2 times (Europe PMC)
  • Research article Hepatitis B Virus Reactivation Risk With IL-17, IL-23/IL-12, or JAK Inhibitors: A Systematic Review and Meta-Analysis [5]
    Alhalabi M, Alshiekh HA · Liver Int · 2026 · cited 1 times (Europe PMC)
  • Research article RSV prophylactics for pediatric populations: A product review and meta-analysis of real-world effectiveness [6]
    Oliva IO, Oliveira CR · Hum Vaccin Immunother · 2026 · cited 1 times (Europe PMC)
  • Research article The Association Between Human Papillomavirus and Prostate Cancer: A Systematic Review and Meta-Analysis [7]
    Botting-Provost S, Ng K, Laurie C, Noorani R, El-Zein M, Franco EL · Int J Cancer · 2026 · cited 1 times (Europe PMC)
  • Research article Transplacental transfer of anti-malarial antibodies: a systematic review [8]
    Belete AM, Camara A, Yazie TS, Amenga-Etego LN, Aniweh Y · Front Immunol · 2026 · cited 1 times (Europe PMC)
  • Research article Liver Cancer Risk and Incidence Attributable to Human Immunodeficiency Virus: A Meta-Analysis and Population-Attributable Modeling Study of Over 1.2 Million Individuals [9]
    Zhao J, Li K, Zhang Y, Chen Y, Xu L, Hu M, et al. · Int J Cancer · 2026 · cited 1 times (Europe PMC)

References

  1. Lindvig SO, Kehrer M, Petersen I, Hess S, Theilgaard ZP, Rosenvinge FS, et al.. Temporal trends in incidence, clinical characteristics and outcomes of pyogenic vertebral osteomyelitis in Southern Denmark from 2009 to 2022: a retrospective population-based cohort study. . 2026. PMID 42902785 · DOI · PMC13689801
  2. Elvis Akem T. Global mpox outbreak dynamics during and after the 2024-2026 public health emergency. . 2026. PMID 42905633 · DOI · PMC13686470
  3. Foox Y, Yamin D, Chalutz-BenGal H, Ben-Gal I. Applying normalized p-control charts for early detection of local COVID-19 outbreaks. . 2026. PMID 42900655 · DOI · PMC13682654
  4. Ozdemir C, Paul T, Egoh K, Wanford JJ, Dekker D, Shawcross DL, et al.. Burden and global distribution of antimicrobial resistance in non-bloodstream infections among adults with cirrhosis: A systematic review and proportional meta-analysis. Int J Antimicrob Agents. 2026. PMID 42208776 · DOI
  5. Alhalabi M, Alshiekh HA. Hepatitis B Virus Reactivation Risk With IL-17, IL-23/IL-12, or JAK Inhibitors: A Systematic Review and Meta-Analysis. Liver Int. 2026. PMID 42287020 · DOI · PMC13263707
  6. Oliva IO, Oliveira CR. RSV prophylactics for pediatric populations: A product review and meta-analysis of real-world effectiveness. Hum Vaccin Immunother. 2026. PMID 42348792 · DOI · PMC13313274
  7. Botting-Provost S, Ng K, Laurie C, Noorani R, El-Zein M, Franco EL. The Association Between Human Papillomavirus and Prostate Cancer: A Systematic Review and Meta-Analysis. Int J Cancer. 2026. PMID 42482406 · DOI · PMC13688217
  8. Belete AM, Camara A, Yazie TS, Amenga-Etego LN, Aniweh Y. Transplacental transfer of anti-malarial antibodies: a systematic review. Front Immunol. 2026. PMID 42404900 · DOI · PMC13328008
  9. Zhao J, Li K, Zhang Y, Chen Y, Xu L, Hu M, et al.. Liver Cancer Risk and Incidence Attributable to Human Immunodeficiency Virus: A Meta-Analysis and Population-Attributable Modeling Study of Over 1.2 Million Individuals. Int J Cancer. 2026. PMID 42277929 · DOI · PMC13547987

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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EvidenceHelix's computed view of the study designs behind this topic: how common meta-analyses, randomized trials and reviews are, how recent the literature is, and a plain-language reading. It describes the design mix of the literature. It is not a quality appraisal of any study, and it is not medical advice.

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Related research topics

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  • Catheter-Related InfectionsInfectious Diseases
  • Community-Acquired InfectionsInfectious Diseases

All 102 articles in Infectious Diseases →

At a glance

3,396,820
PubMed records on this heading
24%
published since 2020
378,919
review articles
65,106
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.

Related topics See all →

  • Focal InfectionInfectious Diseases
  • Opportunistic InfectionsInfectious Diseases
  • Blood-Borne InfectionsInfectious Diseases
  • AnthraxInfectious Diseases
  • Catheter-Related InfectionsInfectious Diseases

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