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Clin Ethics 2008;3:168-170
doi:10.1258/ce.2008.008039
© 2008 Royal Society of Medicine Press

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Five-Minute Focus

Co-payment for medical treatment

Anne Slowther  

Institute of Clinical Education, Warwick Medical School, UK

E-mail: a-m.slowther{at}warwick.ac.uk

In 2004, the then Minister of State for Health in the UK, John Hutton, stated:

‘We strongly believe that the introduction of vouchers, passports, co-payment, or extra charges to patients will have a regressive impact on the health of our people – as all of the international evidence confirms. That is why a patient's passport to personal health should not be dependent on a patient's personal wealth.’1

This unequivocal position now appears to be less secure in 2008 due to a number of factors including:

The specific issue of co-payment for drugs not funded by the NHS is now the subject of a Government-commissioned review of policy in this area, chaired by Professor Mike Richards and expected to report in October 2008. The ethical dilemmas raised by requests from patients to be able to pay for a treatment currently not funded by the NHS but which the patient and clinician consider a desirable treatment option have been discussed previously in this journal and elsewhere.5,6 It is also a problem that is brought to clinical ethics committees and one which challenges us to reflect on the core values of the NHS. In this FMF we will consider the ethical values and arguments underpinning the debate.


    What is co-payment?
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Co-payment for medical care is a feature of many health-care systems. This may be part of the standard health-care package, so that a co-payment (of varying value) is required for every hospital outpatient appointment or GP consultation.7 Or it might be for specific treatments, for example in Germany patients undergoing in vitro fertilization treatment are required to pay 50% of the treatment costs for each cycle.8 Co-payments also occur within the UK NHS although these have tended to be implicit rather than explicit. Thus, GPs will provide private prescriptions for malaria prophylaxis medication while providing some travel immunizations as part of NHS care, or a patient may pay for a private magnetic resonance imaging scan rather than wait for the NHS scan that her consultant has requested. One could argue that prescription charges per se are a form of co-payment. The role of NICE in assessing new technologies and issuing directives on whether specific treatments should be funded by the NHS has thrown the question of co-payment into sharp relief. The focus of the public debate, and the government policy review, is the specific issue of payment by patients for treatment that is not funded by the NHS (often following a NICE recommendation) within the context of a NHS treatment programme. Current policy states that patients wishing to do this should pay for their whole treatment programme privately. It is this specific model of co-payment which we will consider here although the ethical values discussed will be relevant to other models.


    Individual autonomy and the right to choose specific treatments
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A strong argument in favour of allowing co-payments rests on respect for the autonomy of an individual patient to make treatment decisions, including decisions about whether the cost of a specific treatment is worth paying for the potential benefit gained. Decisions about whether to pay for a treatment will be informed by both evidence of clinical effectiveness (it provides some benefit in terms of increased quality or length of life) and cost. However, the value placed on the treatment in terms of how much one is willing to pay for the benefit gained may be very different depending on who is making the judgement. Thus, NICE may consider a treatment too costly in relation to its benefit for the NHS to afford within its budget constraints, but, as Mohindra has pointed out, an individual patient does not make value judgements from the perspective of the NHS as a whole.5 For her the price may be worth paying. To prevent a patient from making that choice would be seen as an infringement of her autonomy.


    Duty of care and the doctor–patient relationship
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The primary duty of a doctor is to make the care of his or her patient their first concern.9 If a doctor considers that a particular treatment would be in his or her patient's best interests, refusal to provide the treatment could be seen as a breach of this duty. It is generally accepted that external constraints, which could include NICE directives, NHS contractual obligations or limited resources, will mitigate this duty to some extent.10 The current debate on co-payments raises the question of whether government policy should constrain a doctor's duty of care to his or her patient in this context.


    Utilitarian arguments for and against co-payment
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Utilitarianism requires that for decisions to be morally acceptable they should maximize overall benefit. A criticism that is often levelled at NICE is that it takes a purely utilitarian view when making its recommendations, considering only the cost-effectiveness of treatments at a population level and ignoring the level of individual need and suffering of patients and their carers.11 This appears to be the crux of the objection to co-payments made by John Hutton in the speech quoted above.1 A critique of the ethics of resource allocation and utilitarianism in general is beyond the scope of this article, but most critics of utilitarianism would concede that when making decisions at a population level within a limited budget, it is desirable to ensure efficient use of resources to benefit the maximum number of people. This may mean that some less cost-effective treatments are not funded. However, supporters of co-payments have argued that they increase efficiency by increasing the number of patients who will benefit from the effective but expensive treatment at no extra cost to the NHS. Thus, the overall benefit will be increased by co-payments.5

The argument for increased efficiency and therefore increased overall benefit from co-payments is based on the assumption that there is no corresponding loss of benefit to patients who do not or cannot choose the co-payment option. If this is not the case, then an assessment of overall harms and benefits would have to be made. For example, if the co-payment treatment required extra resources to be administered or to monitor for toxicity and treat side-effects, then other patients may be harmed by the diversion of resources from their care.


    Consideration of equity in the co-payment debate
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A key argument against co-payments in the UK health system is that they run counter to the NHS founding principle of equal access to treatment based on need and not ability to pay. Permitting co-payments would mean that patients with equal need would be treated differently and thus inequitably. While co-payments will not be restricted to the most affluent in society (some people have been known to sell their house in order to pay for innovative cancer treatments), it is likely that the poorest in society will not be able to benefit from treatments available only through co-payment. Evidence from other countries where co-payment systems have been introduced would suggest that they result in a reduction in health-care utilization that differentially affects those of low socioeconomic status.12,13 In light of the recent publication of the World Health Organization report on health inequity,14 this is a cause for concern. However, in the context of co-payments for specific treatments on the margin of a comprehensive and publicly-funded health-care system such as the NHS, the inequity argument may be less forceful. In this context, co-payment would only be considered for treatments that are not funded as part of the universal package of care available to all patients. If a high quality service is available to everyone and co-payments do not result in resources being diverted from that service, the current equity of access to treatment would be maintained. Indeed, some would argue that it would be more equitable because the extra treatments would be available to a greater number of people than would otherwise be the case.


    Long-term consequences and slippery slopes
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Two ethical concerns regarding co-payments relate to possible long-term consequences for both individual patients and the system as a whole. First, there is a concern that relaxing the rules on paying for non-NICE recommended treatments could result in vulnerable patients being persuaded by pharmaceutical companies to pay for treatments that may not be in their best interests or may even cause them harm. Many patients for whom co-payment may be an option will have serious or terminal disease for which other treatments have failed. These patients may be particularly vulnerable to undue persuasion. A second concern is the possibility that the acceptance of the principle of co-payments will lead to a shift from a universal highest quality possible service with co-payments for marginal treatments to a universal minimum acceptable quality service with co-payments for all other treatments. This scenario would lead to much greater inequities in health-care provision.

The debate on co-payments within a publicly-funded health-care system is ethically challenging. There is a need to balance respect for individual patients' right to make informed choices about their health care, maintenance of the principle of equitable access to high quality health care based on need rather than ability to pay, prevention of diversion of NHS resources to support co-payment treatments and protection of vulnerable patients from undue persuasion to purchase treatments of questionable benefit. The Institute for Public Policy Research (commissioned by the NHS Confederation) has published a discussion document which considers these and other questions around co-payment. They have made a number of recommendations which include:

The report of Professor Richards will provide a further impetus for public debate on this important subject.


    Summary points
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    Footnotes
 
Anne Slowther is Associate Professor in Clinical Ethics at Warwick Medical School, and a practising general practitioner (GP). She joined Warwick in 2006 having previously worked at Ethox. Before moving into academia, she was a full-time GP in Manchester. Anne oversees the National Clinical Ethics Network support programme, which develops and provides support for clinical ethics committees in National Health Service Trusts. Her current work involves teaching medical undergraduates, developing and running educational workshops for members of clinical ethics committees, and supporting the work of priority-setting groups in PCTs. Back


    References and notes
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Go to previous sectionWhat is co-payment?
Go to previous sectionIndividual autonomy and the...
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 References and notes
 

  1. Speech by Rt Hon John Hutton MP, Minister of State (Health), 26 May 2004: The Government and the Private Sector. See http://www.dh.gov.uk/en/News/Speeches/Speecheslist/DH_4083816 (last checked 1 August 2008)
  2. See http://www.nice.org.uk/newsevents/infocus/infocusarchive/OutcomeofJR.jsp (last checked 30 August 2008)
  3. See http://www.guardian.co.uk/society/2008/aug/25/nhs.cancer (last checked 30 August 2008)
  4. See http://news.bbc.co.uk/1/hi/health/7495971.stm (last checked 30 August 2008)
  5. Mohindra RK, Hall JA. Desmond's non-NICE choice: dilemmas from drug eluting stents in the affordability gap. Clin Ethics 2006;1:105–8[Abstract/Free Full Text]
  6. Richards C, Dingwall R, Watson A. Should NHS patients be allowed to contribute extra money to their care? BMJ 2001;323:563–5[Free Full Text]
  7. Holm S, Lis PE, Fritioff-Norheim O. Access to health care in the Scandinavian countries: ethical analysis. Health Care Anal 1999;7:321–30[Medline]
  8. Griesinger G, Diedrich IK, Altgassen C. Stronger reduction of assisted reproduction technique treatment cycle numbers in economically weak geographical regions following the German healthcare modernization law in 2004. Hum Reprod 2007;22:3027–30[Abstract/Free Full Text]
  9. General Medical Council. Good Medical Practice. London: GMC, 2006. See http://www.gmc-uk.org/guidance/good_medical_practice/duties_of_a_doctor.asp (last checked 30 August 2008)
  10. Weinstein MC. Should physicians be gatekeepers of medical resources? J Med Ethics 2001;27:268–74[Abstract/Free Full Text]
  11. A recent example is the reaction to the NICE recommendation on drugs for renal cancer in August 2008
  12. Lostaoa L, Regidorb E, Geyerc S, Aïachd P. Patient cost sharing and social inequalities in access to health care in three western European countries. Soc Sci Med 2007;65:367–76[Medline]
  13. Vardy DA, Freud T, Shvartzman P, et al. Introducing co-payment for consultant specialist services. Isr Med Assoc J 2006;8:558–62[Medline]
  14. World Health Organization Commission on Social Determinants of Health. Closing the Gap in a Generation: Health Equity through Action on the Social Determinants of Health. Geneva: WHO, 2008. See http://whqlibdoc.who.int/hq/2008/WHO_IER_CSDH_08.1_eng.pdf (last checked 30 August 2008)
  15. Institute for Public Policy Research. Topping Up: Should it be Allowed in the NHS? London: NHS Confederation, 2008

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