A Systematic Review of Studies That Aim to Determine Which Outcomes to Measure in Clinical Trials in Children
Background:
In clinical trials the selection of appropriate outcomes is crucial to the assessment of whether one intervention is better than another. Selection of inappropriate outcomes can compromise the utility of a trial. However, the process of selecting the most suitable outcomes to include can be complex. Our aim was to systematically review studies that address the process of selecting outcomes or outcome domains to measure in clinical trials in children.
Methods and Findings:
We searched Cochrane databases (no date restrictions) in December 2006; and MEDLINE (1950 to 2006), CINAHL (1982 to 2006), and SCOPUS (1966 to 2006) in January 2007 for studies of the selection of outcomes for use in clinical trials in children. We also asked a group of experts in paediatric clinical research to refer us to any other relevant studies. From these articles we extracted data on the clinical condition of interest, description of the method used to select outcomes, the people involved in the selection process, the outcomes selected, and limitations of the method as defined by the authors. The literature search identified 8,889 potentially relevant abstracts. Of these, 70 were retrieved, and 25 were included in the review. These studies described the work of 13 collaborations representing various paediatric specialties including critical care, gastroenterology, haematology, psychiatry, neurology, respiratory paediatrics, rheumatology, neonatal medicine, and dentistry. Two groups utilised the Delphi technique, one used the nominal group technique, and one used both methods to reach a consensus about which outcomes should be measured in clinical trials. Other groups used semistructured discussion, and one group used a questionnaire-based survey. The collaborations involved clinical experts, research experts, and industry representatives. Three groups involved parents of children affected by the particular condition.
Conclusions:
Very few studies address the appropriate choice of outcomes for clinical research with children, and in most paediatric specialties no research has been undertaken. Among the studies we did assess, very few involved parents or children in selecting outcomes that should be measured, and none directly involved children. Research should be undertaken to identify the best way to involve parents and children in assessing which outcomes should be measured in clinical trials.
Vyšlo v časopise:
A Systematic Review of Studies That Aim to Determine Which Outcomes to Measure in Clinical Trials in Children. PLoS Med 5(4): e96. doi:10.1371/journal.pmed.0050096
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pmed.0050096
Souhrn
Background:
In clinical trials the selection of appropriate outcomes is crucial to the assessment of whether one intervention is better than another. Selection of inappropriate outcomes can compromise the utility of a trial. However, the process of selecting the most suitable outcomes to include can be complex. Our aim was to systematically review studies that address the process of selecting outcomes or outcome domains to measure in clinical trials in children.
Methods and Findings:
We searched Cochrane databases (no date restrictions) in December 2006; and MEDLINE (1950 to 2006), CINAHL (1982 to 2006), and SCOPUS (1966 to 2006) in January 2007 for studies of the selection of outcomes for use in clinical trials in children. We also asked a group of experts in paediatric clinical research to refer us to any other relevant studies. From these articles we extracted data on the clinical condition of interest, description of the method used to select outcomes, the people involved in the selection process, the outcomes selected, and limitations of the method as defined by the authors. The literature search identified 8,889 potentially relevant abstracts. Of these, 70 were retrieved, and 25 were included in the review. These studies described the work of 13 collaborations representing various paediatric specialties including critical care, gastroenterology, haematology, psychiatry, neurology, respiratory paediatrics, rheumatology, neonatal medicine, and dentistry. Two groups utilised the Delphi technique, one used the nominal group technique, and one used both methods to reach a consensus about which outcomes should be measured in clinical trials. Other groups used semistructured discussion, and one group used a questionnaire-based survey. The collaborations involved clinical experts, research experts, and industry representatives. Three groups involved parents of children affected by the particular condition.
Conclusions:
Very few studies address the appropriate choice of outcomes for clinical research with children, and in most paediatric specialties no research has been undertaken. Among the studies we did assess, very few involved parents or children in selecting outcomes that should be measured, and none directly involved children. Research should be undertaken to identify the best way to involve parents and children in assessing which outcomes should be measured in clinical trials.
Zdroje
1. SulsJRothmanA
2004
Evolution of the biopsychosocial model: prospects and challenges for health psychology.
Health Psychol
23
119
125
2. JonesB
1987
Impairment, disability and handicap.
Child Care Health Dev
13
359
3. NosadiniRTonoloG
2004
Relationship between blood glucose control, pathogenesis and progression of diabetic nephropathy.
J Am Soc Nephrol
15
S1
S5
4. MolenberghsGBurzykowskiTAlonsoABuyseM
2004
A perspective on surrogate endpoints in controlled clinical trials.
Stat Methods Med Res
13
177
206
5. TugwellPBoersM
1993
OMERACT conference on outcome measures in rheumatoid arthritis clinical trials: Introduction.
J Rheum
528
530
6. FlemingTRDeMetsDL
1996
Surrogate end points in clinical trials: Are we being misled.
Ann Intern Med
125
605
613
7. HollowayRGDickAW
2002
Clinical trial end points: On the road to nowhere.
Neurology
58
679
686
8. ClarkeM
2007
Standardising outcomes for clinical trials and systematic reviews.
Trials
8
39
9. DuncanPWJorgensenHSWadeDT
2000
Outcome measures in acute stroke trials: A systematic review and some recommendations to improve practice.
Stroke
31
1429
1438
10. GiacoiaGPBirenbaumDLSachsHCMattisonDR
2006
The newborn drug development initiative.
Pediatrics
117
S1
S8
11. GriffithsAMOtleyARHyamsJQuirosARGrandRJ
2005
A review of activity indices and end points for clinical trials in children with Crohn's disease.
Inflamm Bowel Dis
11
185
196
12. RamseyBWBoatTF
1994
Outcome measures for clinical trials in cystic fibrosis. Summary of a Cystic Fibrosis Foundation consensus conference.
J Pediatr
124
177
192
13. PavleticSZMartinPLeeSJMitchellSJacobsohnD
2006
Measuring therapeutic response in chronic graft-versus-host disease: National Institutes of Health consensus development project on criteria for clinical trials in chronic graft-versus-host disease: IV. Response criteria working group report.
Biol Blood Marrow Transplant
12
252
266
14. GianniniEHRupertoNRavelliALovellDJFelsonDT
1997
Preliminary definition of improvement in juvenile arthritis.
Arthritis Rheum
40
7
1202
9
15. MillerFWRiderLGChungYLCooperRDankoK
2001
Proposed preliminary core set measures for disease outcome assessment in adult and juvenile idiopathic inflammatory myopathies.
Rheumatology
40
1262
1273
16. RupertoNRavelliAMurrayKJLovellDJAndersson-GareB
2003
Preliminary core sets of measures for disease activity and damage assessment in juvenile systemic lupus erythematosus and juvenile dermatomyositis.
Rheumatology
42
1452
1459
17. CarlsonGAJensenPSFindlingRLMeyerRECalabreseJ
2003
Methodological issues and controversies in clinical trials with child and adolescent patients with bipolar disorder: Report of a consensus conference.
J Child Adolesc Psychopharmacol
13
13
27
18. GoldsteinBGiroirBRandolphAMembers of the International Consensus Conference on Pediatric Sepsis
2005
International pediatric sepsis consensus conference: Definitions for sepsis and organ dysfunction in pediatrics.
Pediatr Crit Care Med
6
2
8
19. LaFranceWCJr.AlperKBabcockDBarryJJBenbadisS
2006
Nonepileptic seizures treatment workshop summary.
Epilepsy Behav
8
451
461
20. AnandKJArandaJVBerdeCBBuckmanSCapparelliEV
2006
Summary proceedings from the neonatal pain-control group.
Pediatrics
117
S9
S22
21. ClancyRR
2006
Summary proceedings from the neurology group on neonatal seizures.
Pediatrics
117
S23
S27
22. FinerNNHigginsRKattwinkelJMartinRJ
2006
Summary proceedings from the apnea-of-prematurity group.
Pediatrics
117
S47
S51
23. RothSJAdatiaIPearsonGDMembers of the Cardiology Group
2006
Summary proceedings from the cardiology group on postoperative cardiac dysfunction.
Pediatrics
117
S40
S46
24. ShortBLVanMKEvansJR
2006
Summary proceedings from the cardiology group on cardiovascular instability in preterm infants.
Pediatrics
117
S9
25. LuxALOsborneJP
2004
A proposal for case definitions and outcome measures in studies of infantile spasms and West syndrome: consensus statement of the West Delphi group.
Epilepsia
45
1416
1428
26. SmithMALeederSRJalaludinBSmithWT
1996
The asthma health outcome indicators study.
Aust N Z J Public Health
20
69
75
27. DeRouenTALerouxBGMartinMDTownesBDWoodsJS
2002
Issues in design and analysis of a randomized clinical trial to assess the safety of dental amalgam restorations in children.
Control Clni Trials
23
301
320
28. DalkeyN
1969
The Delphi method: An experimental study of group opinion
Santa Monica (California)
Rand
29. van TeijlingenEPitchforthEBishopCRussellE
2006
Delphi method and nominal group technique in family planning and reproductive health research.
J Fam Plann Reprod Health Care
32
249
252
30. RupertoNRavelliACutticaREspadaGOzenS
2005
The Pediatric Rheumatology International Trials Organization criteria for the evaluation of response to therapy in juvenile systemic lupus erythematosus: prospective validation of the disease activity core set.
Arthritis Rheum
52
2854
2864
31. LewisA
1992
Group child interviews as a research tool.
Br Educ Res J
18
413
421
32. DevaneDBegleyCMClarkeMHoreyDO'BoyleC
2007
Evaluating maternity care: A core set of outcome measures.
Birth
34
164
172
33. RiderLGGianniniEHHarris-LoveMJoeGIsenbergD
2003
Defining clinical improvement in adult and juvenile myositis.
J Rheum
30
603
617
34. HuttonJLWilliamsonPR
2000
Bias in meta-analysis due to outcome variable selection within studies.
R Stat Soc Ser C Appl Stat
49
359
370
35. WilliamsonPRGambleCAltmanDGHuttonJL
2005
Outcome selection bias in meta-analysis.
Stat Methods Med Res
14
515
524
36. ChanAWAltmanDG
2005
Identifying outcome reporting bias in randomised trials on PubMed: review of publications and survey of authors.
BMJ
330
753
37. ConnersCEpsteinJMarchJAngoldAWellsK
2001
Multimodal treatment of ADHD in the MTA: An alternative outcome analysis.
J Am Acad Child Adolesc Psychiatry
40
159
167
38. JuniperEFGuyattGHFeenyDHGriffithLEFerriePJ
1997
Minimum skills required by children to complete health-related quality of life instruments for asthma: Comparison of measurement properties.
Eur Respir J
10
2285
2294
39. RaatHBotterweckAMLandgrafJMHoogeveenWCEssink-BotML
2005
Reliability and validity of the short form of the child health questionnaire for parents (CHQ-PF28) in large random school based and general population samples.
J Epidemiol Community Health
59
75
82
40. DealLGoldBDGremseDAWinterHSPetersSBFragaPDMackMEGaylordSMToliaVFitzgeraldJF
2005
Age-specific questionnaires distinguish GERD symptom frequency and severity in infants and young children: development and initial validation.
J Pediatr Gastroenterol Nutr
41
178
185
41. AnandKJSArandaJVBerdeCBBuckmanSCapparelliEV
2005
Analgesia and anesthesia for neonates: study design and ethical issues.
Clin Ther
27
814
843
42. OsborneJPLuxA
2001
Towards an international consensus on definitions and standardised outcome measures for therapeutic trials (and epidemiological studies) in West syndrome.
Brain Dev
23
677
682
43. RiderLG
2002
Outcome assessment in the adult and juvenile idiopathic inflammatory myopathies.
Rheum Dis Clin North Am
28
935
977
44. RiderLGGianniniEHBrunnerHIRupertoNJames-NewtonL
2004
International consensus on preliminary definitions of improvement in adult and juvenile myositis.
Arthritis Rheum
50
2281
2290
45. OddisCV
2005
Outcomes and disease activity measures for assessing treatments in the idiopathic inflammatory myopathies.
Curr Rheum Rep
7
87
93
46. RupertoNRavelliAOliveiraSAlessioMMihaylovaD
2006
The Pediatric Rheumatology International Trials Organization/American College of Rheumatology provisional criteria for the evaluation of response to therapy in juvenile systemic lupus erythematosus: prospective validation of the definition of improvement.
Arthritis Rheum
55
355
363
Štítky
Interné lekárstvoČlánok vyšiel v časopise
PLOS Medicine
2008 Číslo 4
- Statinová intolerance
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Co dělat při intoleranci statinů?
- Pleiotropní účinky statinů na kardiovaskulární systém
- DESATORO PRE PRAX: Aktuálne odporúčanie ESPEN pre nutričný manažment u pacientov s COVID-19
Najčítanejšie v tomto čísle
- Chile's Neoliberal Health Reform: An Assessment and a Critique
- A Systematic Review of Studies That Aim to Determine Which Outcomes to Measure in Clinical Trials in Children
- Better Reporting, Better Research: Guidelines and Guidance in
- Progress in Vaccination against type b in the Americas