Choosing between randomised and non-randomised studies: a systematic review.
Health Technology AssessmentPublished 1 January 1998Open access
Britton, McKee, Jed Black, McPherson, Colin Sanderson, Bain
Citations312
SJR quartileQ1
SJR score1.36
SNIP1.69
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Abstract
T he overall aim of the NHS R&D Health Technology Assessment (HTA) programme is to ensure that high-quality research information on the costs, effectiveness and broader impact of health technologies is produced in the most efficient way for those who use, manage
Keywords
MedicineEconomics, Econometrics and Finance
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The LancetEfficacy trial of malaria vaccine SPf66 in Gambian infants
192 Citations1995Umberto D’Alessandro, Amanda Leach +9 more
A randomised, double-blind, placebo-controlled trial of SPf66 against clinical P falciparum malaria in Gambian infants, finding protection against clinical attacks of malaria during the rainy season after immunisation in children 6-11 months old at time of the first dose was not achieved.
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179 Citations1994Jonas H. Ellenberg
It is the intent of this paper to present examples of selection bias in a variety of areas which have resulted in misleading or entirely incorrect results to help make research scientifically 'politically incorrect' to the degree that the scientific community 'just says no' to such studies.
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Journal of Clinical OncologySelection bias in clinical trials.
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38 Citations1986J. P. Branagan, Kevin Walsh +4 more
Early treatment with nifedipine did not reduce enzymatically determined infarct size or one month mortality in patients with AMI, or reduce one month morbidity or mortality in Patients with ACI.
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34 Citations1994C. Davis
It is argued that several pieces of information are necessary to determine the extent of extrapolation or generalization warranted in a specific clinical trial.
The LancetResults of a breast-cancer-surgery trial compared with observational data from routine practice
33 Citations1996E Marubini, Ettore Marubini +9 more
Out-trial patients fared no worse than trial patients in terms of survival or distant metastasis after adjustment for baseline characteristics, and the results of clinical trials did not exaggerate the benefits obtainable in routine practice.
The American Journal of CardiologyHemodynamic effects of sublingual nifedipine in acute myocardial infarction
33 Citations1984Gary D. Gordon, Thomas Mabin +4 more
In patients with high initial pulmonary wedge pressures, sublingual nifedipine decreased the wedge pressure more effectively than did 80 mg of furosemide given intravenously and may be useful in patients with early myocardial infarction and left ventricular failure.
Controlled Clinical TrialsRecruiting children and their families for clinical trials: A case study
30 Citations1992William M. Vollmer, Stephanie Hertert +1 more
The recruitment of 226 families for participation in a randomized trial examining the effectiveness of alternative strategies for the management of pediatric asthma found that families of children identified through emergency room and hospital admission records were much more likely to participate in the study.
Age and AgeingHow Useful are Non-random Comparisons of Outcomes and Quality of Care in Purchasing Hospital Stroke Services?
28 Citations1995Patrick Gompertz, Pandora Pound +2 more
A comprehensive district stroke service was not associated with major differences in patient outcomes or standards of care, and service costs, particularly costs of rehabilitation services, were much lower in District 2.
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26 Citations1988L J Walker, Gilbert MacKenzie +1 more
Treatment with nifedipine in the early phase of acute myocardial infarction seems to have no effect on enzymatically measured infarct size.
BMJEffect of non-attenders on the potential of a primary care programme to reduce cardiovascular risk in the population
25 Citations1994Gareth E. Davies, S Pyke +1 more
The intensive follow up of nonattenders resulted in real intervention opportunities in only a small number of families, which should allow for the effect of non-attendance on the overall results.
BMJPatient preferences and randomised clinical trials.
24 Citations1989Chris R. Brewin, C Brewin +17 more
The question is posed, Does morphine treatment increase the likelihood of neuroleptics causing certain involuntary movements?
BMJWhy is the outcome of transient ischaemic attacks different in different groups of patients?
23 Citations1993Graeme J. Hankey, Martin Dennis +2 more
The outcomes of each of three large cohorts of patients with transient ischaemic attacks, which were studied in the same country at much the same time with the same methods, were compared and found to be quite different from each other.
Controlled Clinical TrialsIntercept studies, clinical trials, and cluster experiments: To whom can we extrapolate?
21 Citations1994Charles D. Cowan, Janet Wittes
This paper compares intercept studies and clinical trials with particular emphasis on inference to a population for which the probabilities of being observed are unknown, unreliable, or very small.
Journal of Public HealthThe relationship between evaluative research and audit
21 Citations1992Nick Black
Recognition of the unique and interrelated roles of research and audit will be of benefit to both endeavours.
American Journal of EpidemiologyEfficacy of Measles Vaccines after Controlling for Exposure
20 Citations1993Michel Garenne, Odile Leroy +2 more
The clinical efficacy of measles vaccines was investigated in Niakhar, a rural area of Senegal under demographic surveillance in 1987-1990 using a formal randomized vaccine trial and data from national campaigns using the standard Schwarz vaccine were also analyzed.
Journal of the American Geriatrics SocietyCalcium Antagonists: Antagonists or Protagonists of Mortality in Elderly Hypertensives?
20 Citations1995Curt D. Furberg, Bruce M. Psaty
The objective of treatment of hypertension is to prevent its cardiovascular complications-stroke, acute myocardial infarction, congestive heart failure-not just to lower an elevated blood pressure.
European Journal of Cancer and Clinical OncologyReasons for non-entry of patients with DCIS of the breast into a randomised trial (EORTC 10853)
19 Citations1991I S Fentiman, Jean‐Pierre Julien +4 more
In EORTC trial 10853, patients with histologically confirmed surgical clearance of ductal carcinoma in situ (DCIS) are being randomised to observation alone or to receive external radiation to the breast (50 Gy).
Acta Medica ScandinavicaNon‐respondents in a Post‐myocardial Infarction Trial: Characteristics and Reasons for Refusal
16 Citations1988Pål Smith, Harald Arnesen
Survey of survivors of acute myocardial infarction who refused to participate in the Warfarin Re-Infarction Study found that reasons stated for non-participation reflect poor motivation, low mobility and saturation with focusing on disease.
American Journal of HypertensionQuality-Adjusted Meta-analysis of the Hypertension/Coronary Dilemma
13 Citations1994Ingar Holme, L G Ekelund +2 more
It is concluded that if all randomized drug trials in hypertension had the same treatment efficacy, the estimated CHD prevention would be in the range of 15% and patients at higher risk levels showed better benefit than lower risk patients.
StrokeImproving stroke rehabilitation: a controlled study.
12 Citations1994B Panayiotou, W. Lawrence Beeson
Archives of Internal MedicineA comparison of the study populations in the Diabetes Control and Complications Trial and the Wisconsin Epidemiologic Study of Diabetic Retinopathy
12 Citations1995Ronald Klein
Australian and New Zealand Journal of MedicineSelection of patients for randomised trials: a study based on the MACOP‐B vs CHOP in NHL study
10 Citations1994Janey M. Stone, Christine Laidlaw +2 more
Physician selectivity occurred with respect to patient entry, but trial and non-trial patients were similar in most characteristics, and the trial accrual period could have been 25% shorter.
Journal of Clinical OncologyThe eligibility of women for clinical research trials.
9 Citations1995W. Bradford Patterson, Ezekiel J. Emanuel
American Journal of Clinical OncologyAge as a criterion for eligibility in a lung cancer clinical trial
5 Citations1982Jeannette Y. Lee, James E. Marks +1 more
Age is not an unfavorable prognostic factor for patients with lung cancer and should not be used as a criterion for eligibility in a clinical trial, according to this paper.
ACC Current Journal ReviewEffect of correcting outcome data for case mix: An example from stroke medicine
3 Citations1996
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