Evidence map›Paper›PMID 39927297›Full record

ArticleMedicine international

Prevalence of and risk factors for long COVID following infection with the COVID‑19 omicron variant.

Isao Moritani, Kenji Yamanaka, Tai Nakamura, Junichiro Tanaka, Keigo Kainuma, Masakazu Okamoto, Tomoko Ieki, Hideo Wada, Katsuya Shiraki

Abstract read
In one paragraph

Article in Medicine international. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
  4. Article
  5. Article
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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

9 authors.

Isao MoritaniDepartment of General Internal Medicine, Mie General Medical Center, Yokkaichi, Mie 514-8561, Japan.
Kenji YamanakaSasagawa Clinic of Gastroenterology, Yokkaichi, Mie 510-0961, Japan.
Tai NakamuraNakamura Heart Clinic, Yokkaichi, Mie 510-0892, Japan.
Junichiro TanakaTanaka Internal Medicine Clinic, Yokkaichi, Mie 510-0942, Japan.
Keigo KainumaKainuma Clinic, Yokkaichi, Mie 510-0892, Japan.
Masakazu OkamotoDepartment of Infection Control, Mie General Medical Center, Yokkaichi, Mie 514-8561, Japan.
Tomoko IekiResearch Center, Mie General Medical Center, Yokkaichi, Mie 514-8561, Japan.
Hideo WadaResearch Center, Mie General Medical Center, Yokkaichi, Mie 514-8561, Japan.
Katsuya ShirakiResearch Center, Mie General Medical Center, Yokkaichi, Mie 514-8561, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to clarify the current status of persistent symptoms following omicron variants of COVID-19 [long COVID (LC)] and the risk factors associated with the development of LC. For this purpose, a cross-sectional survey of patients with COVID-19 treated at the authors' hospital and at four associated outpatient clinics was conducted. Questionnaires about a post-infection condition were sent by post to 3,399 patients. A comparison was made of patients infected when the omicron variant was prevalent (omicron group) and patients infected prior to that (pre-omicron group). Valid responses were received from 1,113 (32.7%) patients. The percentages of patients in whom some type of symptom or sequelae continued after 1, 3 and 6 months were 44, 37 and 28%, respectively, in the pre-omicron group, and 20, 12 and 9%, respectively, in the omicron group. The percentages were significantly lower in the omicron group. In the multivariate analysis of risk factors for LC at 3 months, significant risk factors were hospitalization [odds ratio (OR), 1.910; P<0.01] and old age (OR, 1.120; P<0.05). Conversely, the incidence of LC was lower with vaccination (OR, 0.830; P<0.01) and in the omicron group (OR, 0.490; P<0.01). In the omicron group, underlying disease (particularly emphysema, bronchial asthma, rheumatoid or collagen disease and hypertension) and hospitalization were significantly associated with LC (P<0.01). On the whole, the present study demonstrates that the incidence of LC was >10% even in the omicron group. Patients who required hospitalization and patients with underlying conditions require careful attention for the development of LC.

Indexed as

COVID-19long COVIDomicron variant

Identifiers

PMID39927297
PMCPMC11803340

What OpenQuestion holds

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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.