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. 2002 Feb 16;324(7334):425.

Daily regimen and compliance with treatment

All available evidence needs to be evaluated

Knut Schroeder 1,2, Shah Ebrahim 1,2, Tom Fahey 1,2, Alan Montgomery 1,2, Tim Peters 1,2
PMCID: PMC1122345  PMID: 11850382

Editor—Bloom's editorial is a surprising contribution to the important discussion about how best to improve compliance with treatment in chronic diseases.1 His assertion that fewer daily doses increase compliance, and his notion that the least expensive drugs are usually the least effective and have the highest rate of side effects, cannot go unchallenged.

Bloom cites one of his own studies, funded by a pharmaceutical company, to support the idea that fewer daily doses improve compliance.2 This study was a retrospective analysis of prescription records, which showed higher rates of prescription refill at one year among those treated with once daily versus more frequent dosing and those treated with newer, more expensive drugs. The study was confined to supposedly hypertensive patients younger than 71, but no initial blood pressure values were available, and none of them was evaluated in a standardised manner. Moreover, no blood pressure values, non-pharmacological interventions used, side effects, or reasons for stopping treatment were recorded.

Allocation to different drugs was at the discretion of the physician. During the study period, physicians and patients became increasingly aware of the limited benefits of treating mild hypertension in younger patients. Furthermore, it might be expected that a new drug undergoing postmarketing surveillance would be more likely to be continued if financial benefits accrued to the prescriber. Most serious investigators would have been deterred from using such a dataset to tackle the question of compliance, and it is telling that in discussing his findings, Bloom cites one of the landmark trials from the United States in the treatment of hypertension (the hypertension detection and follow up programme) as being from the United Kingdom.

We reviewed the literature on compliance with antihypertensive drugs from 1966 to 1996 and have recently updated our work.3 To our knowledge, at least six randomised controlled trials have investigated the effects of dosing schedules on compliance, with conflicting results.

The notion that the least expensive drugs are the least effective would be a convenient marketing strategy for the pharmaceutical industry, but it is untrue in the two areas Bloom considers. Low dose thiazide diuretics are as effective as more expensive antihypertensive drugs and have a better side effect profile than newer drugs.4,5 For osteoarthritis a recent Cochrane systematic review has reported that paracetamol (acetominophen) is as effective in relieving pain as newer and more expensive non-steroidal anti-inflammatory drugs.

Improving compliance is important—and will undoubtedly involve balancing considerations of efficacy, side effects, and convenience—but better clinical practice will result only from rigorous evaluation of all the available evidence.

References

  • 1.Bloom BS. Daily regimen and compliance with treatment. BMJ. 2001;323:647. doi: 10.1136/bmj.323.7314.647. . (22 September.) [DOI] [PMC free article] [PubMed] [Google Scholar]
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BMJ. 2002 Feb 16;324(7334):425.

Concordance respects beliefs and wishes of patients

Bryan Lask 1

Editor—It was ironic to read in the same issue of the BMJ, Bloom's editorial on compliance and Moscrop's news item, in which he reported that chronically ill patients will have more say in managing their disease.1-1,1-2 Bloom insists on using the term “compliance,” with all its implications that patients should do as their doctor orders them.1-3 He discusses the epidemiology of compliance and the cost of drugs. Nowhere does he refer to the right and need of patients to make their own decisions about their health care or to the reasons why they so often do not adhere to their doctor's advice.

Of course patients will continue to manifest poor adherence to treatment so long as some doctors maintain the attitude that patients should do as we tell them, implicit in the persistent use of compliance, even in editorials in the BMJ. In contrast, Moscrop reports on the aim that patients should become participants in, not just recipients of, their health care. The time has come for us all to participate in “concordance”—an agreement reached after discussion between a patient and healthcare professional that respects the beliefs and wishes of the patient in determining whether, when, and how medicines are to be taken.1-4 It is obvious if we want to achieve optimal treatment.

References

  • 1-1.Bloom BS. Daily regimen and compliance with treatment. BMJ. 2001;323:647. doi: 10.1136/bmj.323.7314.647. . (22 September.) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 1-2.Moscrop A. Expert patients will help manage chronic disease. BMJ. 2001;323:653. . (22 September.) [Google Scholar]
  • 1-3.Dickinson D, Wilkie P, Harris M. Taking medicines: concordance is not compliance. BMJ. 1999;319:787. doi: 10.1136/bmj.319.7212.787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 1-4.Marinker M, ed. From compliance to concordance: achieving shared goals in medicine taking. London: Royal Pharmaceutical Society; Merck, Sharp, and Dohme, 1997.
BMJ. 2002 Feb 16;324(7334):425.

Literature before 1980 should not have been ignored

Alan Porter 1

Editor—In his editorial on compliance with treatment Bloom implies that he searched the literature only since 1980.2-1 Most of the factors influencing compliance had been identified and published by that time. I had provided evidence in the BMJ in 1969 that compliance was better with a once a day dose than with divided doses and confirmed the findings of a number of other workers that old age was not a factor.2-2 It is wrong to ignore the large body of literature that predates 1980.

References


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