Evidence map›Paper›PMID 33013368›Full record

ArticleFrontiers in pharmacology2020

Hematological Malignancy Specific Patient-Reported Outcome Measure (HM-PRO): Construct Validity Study.

Pushpendra Goswami, Esther N Oliva, Tatyana Ionova, Roger Else, Jonathan Kell, Adele K Fielding, Daniel M Jennings, Marina Karakantza, Saad Al-Ismail, Graham P Collins and 5 more

Abstract read
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Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
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  4. Review
  5. Review
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  9. Assessment tools for patient-reported outcomes in multiple myeloma.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
    Review
  10. Observational
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  12. [Application of patient-reported-outcome in myelodysplastic syndromes].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2022
    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

15 authors.

Pushpendra GoswamiSchool of Life and Medical Sciences, University of Hertfordshire, Hatfield, United Kingdom.
Esther N OlivaHaematology Unit, Grande Ospedale Metropolitano, Reggio Calabria, Italy.
Tatyana IonovaSt. Petersburg State University Medical Center and Multinational Centre for Quality of Life Research, St. Petersburg, Russia.
Roger ElsePatient Research Partner, Milton Keynes, United Kingdom.
Jonathan KellCardiff and Vale University Health Board, Cardiff, United Kingdom.
Adele K FieldingUniversity College London Cancer Institute, London, United Kingdom.
Daniel M JenningsRoyal Surrey County Hospital NHS Foundation Trust, Guildford, United Kingdom.
Marina KarakantzaLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Saad Al-IsmailSingleton Hospital, ABM University Health Board, Swansea, United Kingdom.
Graham P CollinsOxford University Hospitals NHS Trust, Oxford, United Kingdom.
Stewart McConnellLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Catherine LangtonLeeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Magda J Al-ObaidiWest Middlesex University Hospital, Isleworth, United Kingdom.
Metod OblakWest Middlesex University Hospital, Isleworth, United Kingdom.
Sam SalekSchool of Life and Medical Sciences, University of Hertfordshire, Hatfield, United Kingdom.

Funding

Cancer Research UK 21019Cancer Research UK 9609
6 · The paper itself

Abstract

backgroundValidity is the ability of an instrument to measure what it claims to measure. It means the degree to which the empirical evidence supports the trustworthiness of interpretations based on the calculated scores. The hematological malignancy (HM) specific patient reported outcome measure (HM-PRO), is a newly developed instrument for use in daily clinical practice as well as in research. This study, provides the evidence for construct validity of the HM-PRO, specifically focusing on the convergent and divergent validity compared to the other established instruments used in hematology.

methodsThis validation study adopted a prospective cross-sectional design where a heterogeneous group of patients diagnosed with different HMs and different disease state were recruited. A total of 905 patients were recruited from seven secondary care hospitals in the UK and online through five patient organizations. Patients were asked to complete the HM-PRO and other cancer specific PRO's, FACT-G and EORTC QLQ C-30. Data analysis was performed using IBM SPSS 23 statistical software.

resultsA total of 486 males (53.7%) and 419 females (46.3%), with a mean age of 64.3 (± 12.4) years and mean time since diagnosis of 4.6 ( ± 5.2) were recruited. The total score of Part A of the HM-PRO highly correlated with the five functional scales of the EORTC QLQ-C30 (Physical = -0.71, Role = -0.72, Emotional = -0.64, Cognitive = -0.58, Social = -0.74-p < 0.001). With respect to correlation with FACT-G, the total score of Part A of the HM-PRO highly correlated with Physical (-0.74), Emotional (-0.57), Functional (-0.66) domains and overall score of FACT-G (-0.74). Similarly, the total score of Part B of the HM-PRO highly correlated with three symptoms scales of EORTC QLQ-C30 (Fatigue scale = -0.74, Nausea and Vomiting = -0.52, Pain = -0.59-p < 0.001) and individual symptom items (Dyspnea = 0.51, Insomnia= 0.43, Appetite loss = 0.54-p < 0.001).

conclusionThe construct validity evidence presented in this research is a testimony to the HM-PRO's ability to measure HRQoL issues which it intends to measure. This is of utmost importance when a PRO is used in routine clinical practice so that the interpretation of the scores or response to an individual item is understood by the clinicians/nurses as intended by the patients.

Indexed as

clinical practiceclinical researchconstruct validityhematological malignancyHM-PROquality of lifesymptoms

Identifiers

PMID33013368
PMCPMC7506039

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