Evidence map›Paper›PMID 37227421›Full record

ArticleClinical and translational allergy2023

The minimal clinically important difference of app-based electronic patient-reported outcomes for hay fever.

Ken Nagino, Jaemyoung Sung, Akie Midorikawa-Inomata, Atsuko Eguchi, Keiichi Fujimoto, Yuichi Okumura, Alan Yee, Kenta Fujio, Yasutsugu Akasaki, Tianxiang Huang and 7 more

Abstract read
In one paragraph

Article in Clinical and translational allergy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Observational
  3. Article
  4. Observational
  5. Article
  6. 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

17 authors.

Ken NaginoDepartment of Hospital Administration, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0317-6074
Jaemyoung SungDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Akie Midorikawa-InomataDepartment of Hospital Administration, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Atsuko EguchiDepartment of Hospital Administration, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Keiichi FujimotoDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yuichi OkumuraDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Alan YeeDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Kenta FujioDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yasutsugu AkasakiDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Tianxiang HuangDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Maria MiuraDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Shokirova HurramhonDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Kunihiko HirosawaDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Mizu OhnoDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yuki MorookaDepartment of Ophthalmology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Hiroyuki KobayashiDepartment of Hospital Administration, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Takenori InomataDepartment of Hospital Administration, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3435-1055

Funding

Japan Agency for Medical Research and Development JP19ek0410063Japan Agency for Medical Research and Development JP23ek0410090Japan Society for the Promotion of Science 20KK0207Japan Society for the Promotion of Science 21K17311Japan Society for the Promotion of Science 21K20998Japan Society for the Promotion of Science 22K16983OTC Self-Medication Promotion Foundation 2019 and 2021Takeda Science FoundationThe Ichiro Kanehara FoundationThe Institute for Environmental & Gender-specific Medicine, Juntendo UniversityThe Kondou Kinen Medical Foundation, Medical Research Encouragement Prize 2020
6 · The paper itself

Abstract

backgroundHay fever is a common allergic disease, with an estimated worldwide prevalence of 14.4% and a variety of symptoms. This study assessed the minimal clinically important difference (MCID) of nasal symptom score (NSS), non-nasal symptom score (NNSS), and total symptoms score (TSS) for app-based hay-fever monitoring.

methodsMCIDs were calculated based on the data from a previous large-scale, crowdsourced, cross-sectional study using AllerSearch, an in-house smartphone application. MCIDs were determined with anchor-based and distribution-based methods. The face scale score of the Japanese Allergic Conjunctival Disease Standard Quality of Life Questionnaire Domain III and the daily stress level due to hay fever were used as anchors for determining MCIDs. The MCID estimates were summarized as MCID ranges.

resultsA total of 7590 participants were included in the analysis (mean age: 35.3 years, 57.1% women). The anchor-based method produced a range of MCID values (median, interquartile range) for NSS (2.0, 1.5-2.1), NNSS (1.0, 0.9-1.2), and TSS (2.9, 2.4-3.3). The distribution-based method produced two MCIDs (based on half a standard deviation, based on a standard error of measurement) for NSS (2.0, 1.8), NNSS (1.3, 1.2), and TSS (3.0, 2.3). The final suggested MCID ranges for NSS, NNSS, and TSS were 1.8-2.1, 1.2-1.3, and 2.4-3.3, respectively.

conclusionsMCID ranges for app-based hay-fever symptom assessment were obtained from the data collected through a smartphone application, AllerSearch. These estimates may be useful for monitoring the subjective symptoms of Japanese patients with hay fever through mobile platforms.

Indexed as

hay feverminimal clinically important differencemobile healthpatient-reported outcome measurespollen allergy

Identifiers

PMID37227421
PMCPMC10151605

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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.