Evidence map›Paper›PMID 34498348›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia2021

Shortening the Haemophilia Activities List (HAL) from 42 items to 18 items.

Isolde A R Kuijlaars, Janjaap van der Net, Tyler W Buckner, Christine L Kempton, Roger E G Schutgens, Kathelijn Fischer

Abstract read
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Validation of the pedHALHaemophilia : the official journal of the World Federation of Hemophilia · 2022
    Article
  6. Review
  7. Article
  8. Shortening the Haemophilia Activities List (HAL) from 42 items to 18 items.Haemophilia : the official journal of the World Federation of Hemophilia · 2021
    Article
  9. 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.

Isolde A R KuijlaarsVan Creveldkliniek, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID https://orcid.org/0000-0003-2920-2258
Janjaap van der NetCenter for Child Development, Exercise and Physical Literacy, University Medical Centre Utrecht, Utrecht University, University Children's Hospital, Utrecht, The Netherlands.
Tyler W BucknerUniversity of Colorado School of Medicine, Aurora, Colorado, USA.
Christine L KemptonHemophilia of Georgia Centre for Bleeding & Clotting Disorders of Emory, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0002-2391-2016
Roger E G SchutgensVan Creveldkliniek, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID https://orcid.org/0000-0002-2762-6033
Kathelijn FischerVan Creveldkliniek, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID https://orcid.org/0000-0001-7126-6613

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe Haemophilia Activities List (HAL) was developed to measure activities and participation in persons with haemophilia (PWH). Shortening the questionnaire may facilitate use of the HAL.

aimThe aim of this study was to determine which items of the HAL are redundant, to construct a shorter version of the HAL, and to determine the construct validity of the HAL

methodsA secondary analysis was performed on pooled data of two published studies using the HAL (seven domains, 42 items, optimum score: 100) in adults with haemophilia A/B. Data were divided into a derivation (62%) and a validation set (38%). Redundant items were identified by evaluation of: floor and ceiling effects, proportions of missing and 'not applicable' responses, inter-item correlations, component loadings in an exploratory factor analysis, internal consistency, and item-total correlations. Correlations with the SF-36 and EQ-5D-5L were used to determine construct validity of the HAL

resultsData on 680 PWH were evaluated. In the derivation dataset (n = 420), median age was 30 years (range 18-80), 43% had severe haemophilia and 61% received prophylaxis. Median (IQR) HAL sum score was 65.0 (55.7-88.8). The stepwise procedure resulted in a HAL

conclusionThis clinimetric study resulted in a >50% shortening of the HAL. The 18-item HAL

Indexed as

Hemophilia AHemophilia BAdolescentAdultAgedAged, 80 and overHumansMiddle AgedQuality of LifeReproducibility of ResultsSurveys and QuestionnairesYoung Adultactivitieshaemophiliaparticipationpatient-reported outcome

Identifiers

PMID34498348
PMCPMC9293145

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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.