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BMJ 2005;330:454-455 (26 February), doi:10.1136/bmj.38337.635648.82 (published 4 February 2005)
Julie Parkes, MRC clinical training fellow1, Deborah L Chase, research fellow1, Andrew Grace, consultant cardiologist2, David Cunningham, technical director, central cardiac audit database3, Paul J Roderick, senior lecturer1
1 Health Care Research Unit, University of Southampton, Southampton SO16 6YD, 2 Papworth Hospital, Cambridge, 3 NHS Information Authority, Tavistock House, London
Correspondence to: J Parkes jules{at}soton.ac.uk
The crude rate of implantation of new ICDs in England rose from 12.4 (95% confidence interval 11.5 to 13.5) per million in 1998 to 30 (28.7 to 31.7) per million in 2002. Regional standardised ratios of use ranged from 0.6 to 1.25 (figure). Significant regional differences in standardised rates of implantation existed (
2 for heterogeneity, P = 0.005), although we found no consistent geographical pattern. Differences between implantation and need in five out of eight regions (95% confidence intervals for standardised ICD implantation and standardised mortality ratio for ischaemic heart disease did not overlap) suggested inequity. A significant inverse relation existed between standardised ICD implantation and fifths of deprivation (P = 0.005, test for trend using a Poisson regression model), ranging from 1.09 to 0.85 (least to most deprived), indicating that an inverse care law may be operating.
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The survey response rate was 74% (26/35). The three most commonly perceived barriers to care for patients eligible for an ICD were identification of patients and referral to implanting centres, staff capacity, and funding for treatment. All of the respondents recorded that they expect to see a large increase in demand for ICDs in the future.
Demand for ICDs will probably increase in the future, particularly in view of expanding indications with randomised evidence of the benefits of ICDs in post-myocardial infarction patients with a low left ventricular ejection fraction.5 Planned expansion of implanting centres and resources are needed to tackle low levels of referral, geographical and social inequity, and the expected increase in demand for ICDs. Strategies should include referral guidelines and targeted education to ensure appropriate identification and referral of eligible patients. These analyses highlight the value of robust national data to inform service development and the need for adequate resources to collect and analyse such information.
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We thank Scot Harris for statistical support and Morag Cunningham, administrator of the national pacemaker and ICD database.
Contributors: JP led the project, cleaned the dataset, did the analyses, constructed the questionnaire and conducted the survey, wrote the first draft of the paper, and is the guarantor. DLC did the analyses, conducted the survey, and helped in writing the paper. AG helped with the survey, commented on drafts, and provided clinical perspective and support to the study. DC is project leader of the national pacemaker and ICD database,provided the 1998-2000 dataset in which data quality and completeness had been improved, and commented on drafts of the paper. PJR oversaw the project, supervised JP and DLC, supplied epidemiology expertise for analyses, and commented on drafts of the paper.
Funding: AG and JP are grant holders of HTA grant 93/23/04 (a review of the evidence on the effects and costs of implantable cardioverter defibrillator (ICD) therapy in different patient groups, and modelling of cost effectiveness and cost utility for these groups in a UK context). Professor Martin Buxton is the principal investigator of this study. DLC is funded by an NHS South East Research and Development Fellowship.
Competing interests: None declared.
Ethical approval: Not needed for this study, as it used aggregated anonymised data and no patient contact.
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