1. An intervention to reassure patients about test results in rapid access chest pain clinic: a pilot randomised controlled trial
- Author
-
Peter Elton, Wendy Colecliffe, Kathryn Hicks, Belen Corbacho Martin, Gill Furze, Kim Cocks, and Anita MacNab
- Subjects
Male ,Health Knowledge, Attitudes, Practice ,Time Factors ,Coronary Disease ,Pilot Projects ,Rapid access chest pain clinic ,Chest pain ,law.invention ,Angina ,Randomized controlled trial ,law ,Non-cardiac chest pain ,Reassurance ,Randomised controlled trial ,Ischaemic heart disease ,Communication ,Middle Aged ,Prognosis ,Brief intervention ,Cardiac surgery ,Coronary heart disease ,England ,Patient Satisfaction ,Predictive value of tests ,Female ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,Research Article ,Adult ,medicine.medical_specialty ,Outpatient Clinics, Hospital ,Patients ,Nurse's Role ,Angina Pectoris ,Patient satisfaction ,Patient Education as Topic ,Predictive Value of Tests ,Intervention (counseling) ,medicine ,Humans ,Pilot study ,Aged ,business.industry ,medicine.disease ,RACPC ,Physical therapy ,Pamphlets ,Nurse-Patient Relations ,business - Abstract
Background Most people referred to rapid access chest pain clinics have non-cardiac chest pain, and in those diagnosed with stable coronary heart disease, guidance recommends that first-line treatment is usually medication rather than revascularisation. Consequently, many patients are not reassured they have the correct diagnosis or treatment. A previous trial reported that, in people with non-cardiac chest pain, a brief discussion with a health psychologist before the tests about the meaning of potential results led to people being significantly more reassured. The aim of this pilot was to test study procedures and inform sample size for a future multi-centre trial and to gain initial estimates of effectiveness of the discussion intervention. Methods This was a two-arm pilot randomised controlled trial in outpatient rapid access chest pain clinic in 120 people undergoing investigation for new onset, non-urgent chest pain. Eligible participants were randomised to receive either: a discussion about the meaning and implication of test results, delivered by a nurse before tests in clinic, plus a pre-test pamphlet covering the same information (Discussion arm) or the pre-test pamphlet alone (Pamphlet arm). Main outcome measures were recruitment rate and feasibility for a future multi-centre trial, with an estimate of reassurance in the groups at month 1 and 6 using a 5-item patient-reported scale. Results Two hundred and seventy people attended rapid access chest pain clinic during recruitment and 120/270 participants (44%) were randomised, 60 to each arm. There was no evidence of a difference between the Discussion and Pamphlet arms in the mean reassurance score at month 1 (34.2 vs 33.7) or at month 6 (35.3 vs 35.9). Patient-reported chest pain and use of heart medications were also similar between the two arms. Conclusions A larger trial of the discussion intervention in the UK would not be warranted. Patients reported high levels of reassurance which were similar in patients receiving the discussion with a nurse and in those receiving a pamphlet alone. Trial registration Current Controlled Trials ISRCTN60618114 (assigned 27.05.2011). Electronic supplementary material The online version of this article (doi:10.1186/1471-2261-14-138) contains supplementary material, which is available to authorized users.
- Published
- 2014