Article

The paper presents some selected results of a survey on Health Technology Assessment (HTA) conducted in twelve OECD countries under the framework of the OECD’s project on Health-related technologies.
The definition and functions of HTA are described.
The five case study technologies taken under consideration were: positron emission tomography, hepatitis C genotyping and viral load testing, telemedicine, prostate cancer screening and stroke technologies.
Useful insights into the production of HTA in survey countries were obtained but care needs to be taken before generalising the results.

The OECD initiated the Health Project in 2001 to address some of the key challenges policy makers face in improving their country’ health systems.
Health care is an important economic, scientific and social endeavour for all OECD countries. It has contributed to the extension of human life and reduction of pain, disease risk, and disability. However, in recent decades health-related activities have been consuming growing proportions of GDP. In 1990, the average rate of health care spending in OECD countries was 7.3% of GDP. By 2001, this average had risen to 8.4% - representing an increase of 15% over and above GDP growth (OECD 20021).
In the context of lower economic growth, the ageing of the population and the rise in health care prices and utilisation, many OECD governments are concerned about the sustainability of public health care financing.
A desire for real progress and recognition of important gaps in the information needed to undertake change led to political commitment and support across countries for a focused cross-national effort. The three-year initiative provided member countries with multiple opportunities to participate in and learn from component studies focused on pressing health policy issues and to benefit from the information and exchanges that occurred.
The final report2 published by the OECD at the occasion of the meeting of the OECD Health Ministers held at Paris, 13 – 14 May 2004 begins by investigating the potential for further improvements through disease prevention and health-care quality improvement. It next considers approaches for resolving outstanding problems in fostering adequate access to care. The report then explores avenues for increasing the responsiveness of health systems. The cost and financing dilemma and the prospects for increasing efficiency are also considered.
As part of the OECD Health Project, a study on health-related technologies (see box 1 for a definition of health technology) was launched due to observations reported by some authors regarding the fact that technology is a driver of health care costs, e.g. Aaron3(1991) and Newhouse4 (1992) report that approximately 50% of the rise in health care spending can be attributed to technological change. Furthermore, a study by Fuch5 (1996) indicates that this proposition has become a dominant view amongst health economists. However, other economists argue that there is little direct evidence on the role of technological change in cost growth (Cutler and McClellan, 1996)6.

What is a health technology?
Health technologies are means to improve health outcomes at the population or individual levels. They may include processes, expertise, systems, or artefacts. Drugs, an MRI scanner, a patient recall system for population cervical screening, a stent, minimally invasive approaches to surgery, and a patient records management system, are all health technologies in this sense. Of course, drugs, capital equipment and devices tend to be the technologies that get the most attention from most of the stakeholders.

The OECD’s project on health related technologies
The OECD’s project on health related technologies, conducted under the guidance of experts drawn together from government, academia, health technology assessors and industry, has aimed to provide evidence on how countries can improve the integration of health care technologies. Its focus has been on the transition from Health Technology Assessment (HTA) to decision making and decision implementation. It examined the production of evidence, primarily in the form of HTA, and the use of evidence in decision making. It has also examined features of the decision making process and the policy tools used to implement decisions. Fundamentally, the project has asked two questions:
How can the use of evidence be improved in health care decision making?
How can the decision making and implementation processes be improved to deliver better health system performance?
The project sought to survey current practice in decision making and implementation, and the use of HTA; to identify and consider the key challenges in decisionmaking
and using HTA in reaching decisions; and to discuss and validate the results in an expert wor shop.
This paper presents a description of Health Technology assessment; its principal functions and some selected results of the survey. For the overall description of the project see ref.7

Health Technology Assessment: the technology of decision making
Health Technology Assessment is best understood as a set of methods for the systematic organisation and appraisal of information around health technologies. There is a large international community involved in HTA and supported by various cross-country projects and associations, including Health Technology International, (HTAi)8 (under the auspices of which is published the International Journal of Technology Assessment in Health Care), and the International Network of Agencies for Health Technology Assessment (INAHTA)9, membership of which is comprised of organisations that are majority-funded by governments.
The HTA process comprises two stages. First there is the systematic review of evidence which includes:
Identification of a research question, for example, “what is the additional benefit of polymerase chain reaction over cytogenetics in diagnosis of haematological malignancy?”, or “what is the optimal strategy for management of lower back pain?”, and development of a research strategy to answer these questions.
Systematic retrieval of scientific evidence.
Analysis, critical review and summary of the evidence, including comment on the validity and strength of the evidence.
Though it is strictly not ‘review’, this component of HTA may also include modelling, especially to support economic analysis.
The second stage is appraisal. That is, forming judgements about the meaning of the evidence obtained by systematic review and the formation of views as to the value of a technology in the health care system. The evidence and its appraisal then inform the decision making process10.
At minimum, HTA directed to particular technologies addresses safety and effectiveness of those technologies; that is, what risks obtain to patients and whether they are justified given the possible health gains; and whether the technologies provide beneficial health outcomes and how those health outcomes compare with alternative technologies.
Very frequently HTA includes economic evaluation, typically in the form of cost-effectiveness analysis (CEA). It is important to note that CEA asks a different question from cost-benefit analysis (CBA). CBA and CEA ask a similar question in the general terms, “are the costs of an investment justified by its costs? “ Unlike CBA, CEA measures outcomes in natural units of health benefit rather than in monetary terms. Ideally these measures are a multi-dimensional unit such as quality-adjusted life years, or a unit of life years saved; or less ideally, units such as numbers of events of morbidities avoided (for example, cost per acute myocardial infarction avoided).
The specific question for CEA tends to be: “if a technology will provide net health gains for the community, and if the technology costs more than the alternatives (and they usually do), what is the cost per unit of health gain and is that a worthwhile investment for the community?”
HTA Functions
The principal functions of HTA have been defined by the members of the International Network of Health Care Technology Agencies (INAHTA) as:
Technology Safety: To assess the potential adverse effects of diagnostic and therapeutic technologies.
Efficacy and Effectiveness: To assess the capacity of technologies to produce beneficial effects, both in ideal and real situations.
Efficiency (economic evaluation): Once the effectiveness of the technology has been tested, it is necessary to evaluate its efficient application in the system.
Social consequences (intended and unintended): It is then necessary to assess the social consequences of the application of the technology. This includes the assessment of equity, as well as the opportunity cost associated with the use of technology.
Ethical implications: To consider the ethical implications of decisions about the incorporation of new technologies (e.g. cloning).
Acceptability, availability, accessibility, and utilisation indications: This final step includes the assessment of operative issues about the incorporation and use of medical technology.
Survey on how some OECD countries integrate Health Technologies and the use of HTA
The survey focused on past and present decision-making processes and production of HTA, seeking information on: How decisions about health technologies are made; how evidence, and in particular HTA, was used in that decision; how HTA was conducted and how decisions were implemented within health care systems.
The survey examined three types of decision making (i) pre-marketing decisions: the decision to allow a product/service to be used in the health care system; (ii) funding/coverage decisions: the decision to fund/cover a product or service on either private or public insurance schemes; and (iii) investing/planning: the decision to invest in a technology, including health care planning decisions. The survey analysis primarily focused on funding/coverage and investing/planning decisions.
To enable collection of comparative information the survey collected information for five case study technologies11: positron emission tomography, hepatitis C genotyping and viral load testing, telemedicine, prostate cancer screening and stroke technologies. These technologies were selected by the Expert Group based on an agreed set of criteria. These criteria aimed to ensure that the selection of case study technologies would reflect the diversity of uses (e.g. use of technology in screening, diagnosis, treatment, and management) and settings (e.g. ambulatory care, hospital care). Together, the set of case study technologies illustrate decision making in various parts of the health care system.
Twelve countries participated in the survey. These were: Australia, Austria, Canada, France, Germany, Ireland, Japan, Mexico, The Netherlands, Norway, Spain and Switzerland. Survey respondents were identified by members of the Expert Group and nominated on the basis of their expertise in either the decision making process and/or the production of HTA for any of the five case study technologies. Survey respondents included departmental officials, health technology assessors, health care and hospital administrators, clinicians and researchers.
The production of health technology assessment : an analysis of survey results
The following results are based on health technology assessments carried out on a sample of case study technologies. Whereas they provide useful insights into the production of HTA in survey countries, care needs to be taken before generalising the results.
Who undertakes HTA?
Chart 1 shows that the most common practitioners of HTA were not-for-profit agencies who conducted 27% of all HTAs in this sample (n=26). It also shows that joint assessments were common. Joint assessment always included a not-for-profit agency together with a professional body and/or government. (Chart 1)

What is inside HTA?
The OECD survey found that the content of HTA varied quite significantly for the five case study technologies. Table 1 demonstrates that while almost all HTAs included evidence of effectiveness (with only one exception in telemedicine), there were far fewer assessments that considered psychological, social and ethical factors. Cost-effectiveness was also reported widely, but additional costs or cost savings less so. Fewer HTAs reported taking R&D issues into consideration.

Click here to see the Table 1

What led to HTA being conducted?
The OECD survey asked respondents to identify the reasons for carrying out a HTA. Table 2 shows that in this survey the most common reason for undertaking an HTA was that it was part of an existing HTA programme. However, there is some interesting variation between technologies. For example, the primary reason for an assessment of costly technology such as Position Emission Tomography was a direct request from the government or insurer. However an assessment of telemedicine was more likely to have been conducted as part of a HTA programme. The other reasons for undertaking HTA included political pressure and priority for a national research or HTA programme.

Click here to see the Table 2

Who and what is the HTA for?

Different OECD countries have different purposes for HTA. Some countries have instigated (or are in the process of instigating) formal consideration of economic evidence in decision making, particularly for pharmaceutical reimbursement decisions (Dickson, Hurst and Jacobzone, 200312).
Beyond pharmaceutical technologies, the survey found that for the five case studies, the most commonly envisioned role for the HTA was to inform providers, closely followed by the role of informing investment decisions. As demonstrated in Chart 2, 8% of respondents sited other roles for the HTA, which mainly involved health services planning.
(Chart 2)

The timing and resources required for HTA
The survey asked respondents to estimate the time it took to complete the HTA. The results from 19 different HTAs show that some HTAs take less than a month while others take up to four years. Table 3 reports the percentage of HTAs in the survey by the amount of time taken.
(Table 3)

Click here to see the Table 3


Marketing HTA activities
The survey received 16 responses to the question of how HTA results were disseminated. Chart 3 shows that most HTA practitioners use multiple means of distributing the results of HTA. The most common forms of dissemination were: widely distributing reports or newsletters, website publication, and conferences and meetings.
A number of respondents mentioned that they used different methods of dissemination to target various audiences.
That is, they established a portfolio approach to dissemination depending on the key messages of the HTA and who the decision makers were.
Chart 3. Methods of disseminating HTA


Conclusions

Health technologies can convey enormous benefits to health, but may account for up to half of the increased costs in health care. Health care decision makers face the challenging task of harnessing the opportunities created by health technologies and at the same time ensuring that the health care system remains sustainable and equitable. Adding to this challenge are the sometimes conflicting pressures and demands from patients (and tax payers), health professionals, the producers of new technologies, and a range of other pressure groups.
Objective evidence is of crucial importance in helping to resolve conflicting demands to reach transparent agreement on the optimal paths forward. Without evidence, the uptake and diffusion of technologies are more likely to be influenced by a whole range of social, financial, professional and institutional factors, and may not produce optimum levels of health outcomes.
HTA is a form of assessment which considers not only the effectiveness of technologies but also their wider impacts, including legal and social issues and efficiency. The role of HTA is highly valued by decision makers and is playing an increasing role in many OECD countries.