Evidence map›Paper›PMID 40770795›Full record

SynthesisBMC public health2025

The impact of the COVID-19 pandemic on melanoma diagnosis: a systematic review and meta-analysis of global evidence.

Seyed Mostafa Mostafavi Zadeh, Elahe Noroozi, Elmira Gheytanchi, Fatemeh Tajik, Zahra Madjd, Davoud Ahmadvand

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Seyed Mostafa Mostafavi ZadehOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Elahe NorooziOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Elmira GheytanchiOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Fatemeh TajikOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Zahra MadjdOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran. zahra.madjd@yahoo.com.
Davoud AhmadvandDepartment of Molecular Imaging, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran. d.ahmadvand@iums.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe COVID-19 pandemic significantly disrupted healthcare systems worldwide. Prioritizing emergency responses resulted in the postponement of routine medical care, including melanoma diagnoses. We performed a systematic review and meta-analysis to quantify the pandemic's effect on diagnosis rates, Breslow thickness, stage at presentation, ulceration, histologic subtypes, and patient age.

methodWe performed a systematic review and meta-analysis following PRISMA guidelines. PubMed, Scopus, Web of Science, and Embase were searched up to 10 September 2024 for observational studies comparing melanoma outcomes in the pre-COVID era (before March 2020) with the COVID era (March 2020 onwards). Two reviewers independently screened records, extracted data on diagnostic counts, patient age, Breslow thickness, ulceration, and histopathological subtype, and assessed study quality using the Newcastle-Ottawa Scale (NOS). Random-effects models pooled rate ratios (RRs) or odds ratios (ORs); fixed-effects models pooled mean differences (MDs). Heterogeneity was evaluated with I², and sensitivity analyses were restricted to high-quality studies (NOS ≥ 7).

resultsSixty-two studies (38,676 pre-COVID and 46,846 COVID-era melanomas) met inclusion criteria. New melanoma diagnoses fell by 19% during the pandemic (RR = 0.81, 95% CI 0.75-0.86; I² = 98%). Mean age at diagnosis rose by 0.86 years (95% CI 0.58-1.14; I² = 45%). Tumors were thicker (MD = 0.24 mm, 95% CI 0.02-0.47; I² = 92%) and more frequently ulcerated (OR = 1.29, 95% CI 1.15-1.44; I² = 31%). Nodular melanoma, an aggressive subtype, became more common (OR = 1.34, 95% CI 1.08-1.67; I² = 81%), whereas superficial spreading, acral lentiginous, and lentigo-maligna subtypes showed no significant change. All the key findings persisted in good-quality-only analyses.

conclusionCOVID-19-related service disruptions were associated with fewer melanoma diagnoses but a shift toward older patients and biologically adverse tumor features, signaling delayed detection at the population level. Strengthening resilient, rapid-access skin cancer pathways and integrating tele-dermatology with triaged in-person assessment are public-health priorities for future crises.

trial registrationPROSPERO registration number CRD42022361569.

Indexed as

COVID-19MelanomaSkin NeoplasmsGlobal HealthHumansPandemicsBreslow thicknessCancer diagnosisCOVID-19MelanomaMeta-analysisNodular melanomaSystematic reviewUlceration

Identifiers

PMID40770795
PMCPMC12326724

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Registered trials

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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.