BMJ 1998;316:736-741 ( 7 March )

Papers

Variations in population health status: results from a United Kingdom national questionnaire survey

Paul Kind, senior research fellowPaul Dolan, research fellowClaire Gudex, research fellowAlan Williams, professor of economics

Centre for Health Economics, University of York, York YO1 5DD

Correspondence to: Dr Kind pk1{at}york.ac.uk

    Abstract
Top
Abstract
References

Objective: To measure the health of a representative sample of the population of the United Kingdom by using the EuroQoL EQ-5D questionnaire.
Design: Stratified random sample representative of the general population aged 18 and over and living in the community.
Setting: United Kingdom.
Subjects: 3395 people resident in the United Kingdom.
Main outcome measures: Average values for mobility, self care, usual activities, pain or discomfort, and anxiety or depression.
Results: One in three respondents reported problems with pain or discomfort. There were differences in the perception of health according to the respondent's age, social class, education, housing tenure, economic position, and smoking behaviour.
Conclusions: The EQ-5D questionnaire is a practical way of measuring the health of a population and of detecting differences in subgroups of the population.

Key messages

  • Measurement of health outcome requires the observation of states of health

  • Patients' involvement in recording and assessing their own state of health is a major element in the process of evaluating the impact of health care

  • The EuroQoL EQ-5D questionnaire highlights variations in states of health which are consistent with previously published results

  • High degrees of pain are reported in the general population. A category for pain is absent and thus undetected in the survey of disability by the Office of Population Censuses and Surveys


    Introduction

The measurement of health is central to the evaluation of health care. By observing the extent of changes in health the benefits and disbenefits of health care for both patients and groups of patients can be evaluated; over the past 25 years several generic measures of health have been developed for use in this way.1-8 These instruments were designed for use as general purpose measures of health, independent of diagnostic categorisation or disease severity. Information based on such measures is useful for establishing the degrees of morbidity in the community, enabling different population subgroups to be compared, which would help in assessing health needs or in informing those responsible for allocating health resources. Periodic reassessment of health could provide important data on the extent of any changes in the health of a population---for example, the extent to which the population is achieving national targets for health. If such standardised information was also routinely collected on individual patients it would provide a simple means of evaluating the outcomes of their health care.

We report on a study in which the EuroQoL EQ-5D questionnaire9 was fielded in a survey of the population of the United Kingdom, conducted as part of a wider study of practical ways of measuring health related quality of life.10

    Subjects and methods

EQ-5D questionnaire
The EQ-5D questionnaire is a generic measure of health status developed by the EuroQoL Group, an international research network established in 1987 by researchers from Finland, the Netherlands, Sweden, and the United Kingdom. The EQ-5D questionnaire defines health in terms of five dimensions: mobility, self care, usual activities (work, study, housework, family, or leisure), pain or discomfort, and anxiety or depression. Each dimension is subdivided into three categories, which indicate whether the respondent has no problem, a moderate problem, or an extreme problem (appendix). Combinations of these categories define a total of 243 health states. The EQ-5D questionnaire comprises two pages; on the first page respondents record the extent of their problem in each of the five dimensions and on the second page they record their perception of their overall health on a visual analogue scale (0 denoting the worst imaginable health state and 100 denoting the best imaginable health state). The validity and reliability of the EQ-5D questionnaire have been tested,11-13 as has its application in a range of patient groups.14-16 Since the original survey reported here, the EQ-5D questionnaire has been fielded in three national surveys, including the English national health survey---an interview-based survey of about 16 000 people. The EQ-5D questionnaire has also been used in population surveys in Spain, Germany, and Canada.

Survey design and methods
Members of the public aged 18 and over were interviewed as part of a national survey. No upper age limit was stipulated. The sample was based on addresses in England, Scotland, and Wales, selected by postcode.17 Eighty postcode areas were chosen, proportionately to the number of addresses in each area, after these areas had been stratified by regional health authority, socioeconomic group, and population density. Seventy six addresses were selected from each postcode area, yielding a total of 6080 addresses. At each of these addresses one adult aged 18 or over was selected using a Kish grid.18 Individuals in institutions, hostels, care homes, or bed and breakfast accommodation were excluded from the sample. Of the selected addresses, 12% were unproductive as they were non-residential, empty, or untraceable. The final sample comprising 3395 subjects was representative of the general population with respect to age, sex, and social class. During the interview, respondents completed the EQ-5D questionnaire and provided information on age, sex, marital state, education, employment, housing tenure, and smoking behaviour. The interviews took place during the last quarter of 1993. 

Analysis mainly compared the differences between the population subgroups. It was hypothesised that more health problems would be reported with increasing age, with lower social class, for those registered sick or disabled, and for smokers. chi 2 Tests were used for the analysis of the descriptive profile data, and Student's t test was used to test for subgroup differences in the visual analogue scale data.

    Results

A moderate problem on at least one dimension was reported by 42% of respondents, whereas only 6% of respondents reported any extreme problem (table 1). Problems were most often recorded in the pain or discomfort dimension. In subsequent analyses, moderate and extreme categories of each dimension were combined.

                              
View this table:
[in this window]
[in a new window]
 

Table 1 Numbers (percentages) of respondents reporting a problem in each EuroQoL dimension

The mean state of health recorded on the visual analogue scale was 82.5 (SD 17).

Health and age
The rates of reported problems increased significantly with age (P<0.001) for all dimensions (table 2); an exception to this general pattern was the anxiety/depression dimension, which peaked at 28% of respondents aged 60 to 69 and then decreased slightly.

                              
View this table:
[in this window]
[in a new window]
 

Table 2 Numbers (percentages) of respondents reporting any problem, by age group and sex

Figure 1 shows the mean visual analogue scale values for each age group and the 95% confidence interval. The mean value decreased from about 87 in the youngest age group to 72 in the oldest age group. Mean values did not differ significantly in the 20 to 49 age range but decreased significantly for respondents aged >= 50 (P<0.001).

Health and sex
Women aged >= 70 tended to report higher rates of problems than did men of the same age (table 2). A systematic difference in rates was found across all age groups on the anxiety/depression dimension, with women reporting significantly higher rates than men (P<0.05). No significant differences were found in the visual analogue scale scores for men and women.


View larger version (17K):
[in this window]
[in a new window]
 
Fig 1.    Mean self rated health status of respondents

Health and marital status
Respondents who were widowed, separated, or divorced reported significantly more problems on all five dimensions (P<0.001). Scores on the visual analogue scale for this group were also significantly lower than for respondents living alone or for those with a partner (means 77, 84, and 84 respectively, P<0.001).

Health and social class
After the effects of age were controlled for, there were significant differences in the rates of reported problems when respondents were grouped according to social class (table 3).

                              
View this table:
[in this window]
[in a new window]
 

Table 3 Numbers (percentages) of respondents reporting any problem, by age group and social class (based on respondent's own current or most recent occupation as classified by registrar general)

Rates of reported problems from respondents in social classes III and IV were between 20% and 120% higher than rates in respondents from social classes I and II; the largest differences were for the pain/discomfort (P<0.01) and anxiety/depression (P<0.01) dimensions. Rates did not differ significantly for the mobility and self care dimensions. Figure 2 shows that respondents from social classes I and II had consistently higher levels of reported health as measured by the visual analogue scale than respondents from the two other social classes. Respondents from social classes I and II had a 5 point advantage on the visual analogue scale over respondents from social classes IV and V of the same age group. The difference was significant for all age groups except for respondents aged 40 to 49 years. The mean scores on the visual analogue scale for respondents from social classes I and II remained above the level of the youngest respondents from social classes IV and V until the 50 to 59 age group.


View larger version (26K):
[in this window]
[in a new window]
 
Fig 2.   Effect of social class on self rated health status. *P<0.05; **P<0.01; ***P<0.001

Health and education
When respondents were classified by education rather than by social class, a similar pattern of differences emerged. Respondents who had received higher or further education reported significantly lower rates of problems with mobility (P<0.05), usual activities (P<0.05), pain/discomfort (P<0.01), and anxiety/depression (P<0.01) than did those who had received no education after leaving school. A similar pattern was seen on the visual analogue scale, with significantly higher scores reported for those who had received higher or further education (P<0.001).

Health and economic status
Significantly higher rates of problems were reported by respondents who were unemployed, sick or disabled, or retired, compared with those in employment or full time education (P<0.001) (table 4). Rates of reported problems for unemployed people were almost twice those of respondents in a salaried job.

                              
View this table:
[in this window]
[in a new window]
 

Table 4 Numbers (percentages) of respondents reporting problems, by employment

When respondents were grouped according to housing tenure, significantly higher rates of problems were recorded on all the dimensions for those living in rented property compared with owner occupiers.

The mean scores on the visual analogue scale of people in work or of people who were studying was significantly higher than for people who were unemployed (87.5 and 82.0 respectively, P<0.001). Similarly, the scores of owner occupiers were significantly higher than for people who rented their accommodation (85.1 and 77.2 respectively, P<0.001).

Health and smoking behaviour
Respondents who smoked reported significantly higher rates of problems than non-smokers on all dimensions. Non-smokers also recorded significantly higher scores on the visual analogue scale than respondents who smoked (83.4 and 80.4 respectively, P<0.001).

Analysis of variance
Analysis of variance was used to investigate the collective influence of background variables. With the score on the visual analogue scale as the dependent variable and age as a covariate, a main effects model indicated a significant contribution for education (P<0.01), employment (P<0.001), and smoking behaviour (P<0.001). Housing tenure, marital status, and social class were not significant variables in this model.

Disability rates from other national surveys
Respondents who reported any problem in any dimension could be distinguished from respondents who reported no problems whatsoever. This dichotomy can be used to form an arbitrary definition of disability, enabling data to be compared with the findings of other surveys. The general household survey incorporates questions on longstanding illness and recent interference with usual activities.19 The responses to these questions are combined to give rates of limiting longstanding illness which are published annually. The disability survey by the Office of Population Censuses and Surveys conducted in 1985 included a questionnaire comprising 10 categories: locomotion, reaching and stretching, dexterity, seeing, hearing, personal care, continence, communication, behaviour, and intellectual functioning.20 The rates of disability in people grouped into five year age groups were reported in this survey.20 These data were plotted against disability rates determined from our survey (fig 3). Disability rates based on responses to the EQ-5D questionnaire were 20% to 25% higher than rates from the general household survey for all age groups and about 30% to 40% higher than the 1985 disability survey, until the age of 80. 


View larger version (24K):
[in this window]
[in a new window]
 
Fig 3.   Disability rates from three national surveys

    Discussion

This survey provides an important insight into the health status of the population of the United Kingdom at any one time. Although extreme problems with mobility and self care were rarely reported in this survey, there was a high level of reported problems with pain or discomfort. Over 50% of respondents aged >= 70 and about 20% of the youngest respondents reported some problem in this dimension. This finding has important implications. Pain does not seem to be a dimension of interest in a national disability survey despite being widely experienced in the community. The omission of a pain category means that it is assigned a zero weight, despite good evidence that it has a powerful influence on society's valuations of states of health.21 These factors combine to disadvantage a significant proportion of the general population.

Significant differences were found between population subgroups with respect to age, social class, marital status, employment, education, and smoking behaviour. These findings compare with findings reported elsewhere.22-24 Disability rates based on the EuroQoL classification reflected similar trends to those seen in the general household survey and surveys of the Office of Population Censuses and Surveys, although rates in these surveys were somewhat lower as they were based on a narrower definition of disability.

Population averages
The representativeness of the survey suggests that the results are indicative of the average health status in the general population of the United Kingdom, although it should be borne in mind that sampling was limited to individuals living in the community and tended to exclude people who had extreme problems with mobility or with self care and therefore likely to be dependent on others for their daily needs. Current investigation of specific patient groups---for example, people attending their general practice surgeries---reveals a wider distribution of reported problems. Thus, to the extent that this survey excluded people who were likely to yield responses indicating more severe problems, the results may well underestimate the health related quality of life of the general population.


View larger version (37K):
[in this window]
[in a new window]
 
Appendix

EQ-5D questionnaire


Our data can be treated as descriptive population "norms." As such, they could provide baseline values for monitoring variations in health for specific population groups, particularly if this information was also linked to local epidemiological data. In aggregate form, such information could be used to complement national targets by providing a measure based on health status rather than mortality. The capacity of the EQ-5D questionnaire to generate quantifiable and usable information on the health status of a population led to its inclusion in the 1996 health survey for England.25

Measuring outcomes
However, it is the measurement of change in health status for which the need is greatest. There can be few circumstances in which healthcare workers are not concerned with the measurement of outcome, and the EQ-5D questionnaire provides the capacity to measure change in health status, and hence outcomes, in a simple standardised way. The information on self reported problems recorded on the first page of the EQ-5D questionnaire identifies a unique health status for which there is a corresponding index value based on the views of the general population.21 Changes in health status and the value of that change can be used to quantify outcomes for clinical and economic evaluation; the latter role was recommended for the EQ-5D questionnaire in a report commissioned by the United States Department of Public Health.26 There is "an increasing consensus regarding the centrality of the patient's point of view in monitoring medical care outcomes,"6 and the EQ-5D questionnaire has the obvious potential to contribute to that process. The national survey data reported in this paper show what can be achieved by using an uncomplicated instrument for measuring health status. The further exploitation of its potential is open to us all.

    Acknowledgments

Survey work for the 1993 survey was conducted by Social and Community Planning Research, and we thank the trained fieldwork staff for their help in the collection of the data.

Contributors: All four authors shared equally in the design and execution of the research reported in this paper. Social and Community Planning Research provided significant additional expertise in the design and management of the national survey. PK will act as guarantor for the paper.

Funding: The project was funded by the Department of Health. The views expressed are those of the authors and not necessarily of the Department of Health.

Conflict of interest: None.

    References
Top
Abstract
References

  1. Patrick DL, Bush JW, Chen MM. Methods for measuring levels of well-being for a health status index. Health Serv Res 1973; 11: 516.
  2. Rosser RM, Watts V. The measurement of hospital output. Int J Epidemiol 1972; 1: 361-368[Abstract/Free Full Text].
  3. Bergner M, Bobbitt RA, Kressel S, Pollard WE, Gilson BS, Morris JR. The sickness impact profile: conceptual formulation and methodology for the development of a health status measure. Int J Health Serv 1976; 6: 393-415[Medline].
  4. Hunt SM, McKenna SP, McEwen J, Backett EM, Williams J, Papp E. A quantitative approach to perceived health status: a validation study. J Epidemiol Community Health 1980; 34: 281-286[Abstract/Free Full Text].
  5. Torrance GW, Furlong W, Feeny D, Boyle M. Multi-attribute preference functions. Pharmacoeconomics 1995; 7: 503-520.[Medline]
  6. Ware JE, Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care 1992; 30: 473-483[Medline].
  7. Sintonen H. An approach to measuring and valuing health states. Soc Sci Med 1981; 15: 55-65.
  8. EuroQoL Group. EuroQoL---a new facility for the measurement of health-related quality of life. Health Policy 1990; 16: 199-208[Medline].
  9. Brooks RG. EuroQoL---the current state of play. Health Policy 1996; 37: 53-72[Medline].
  10. Williams AH. The measurement and valuation of health: a chronicle. University of York: Centre for Health Economics , 1995(Discussion paper 136.)
  11. Brazier J, Jones N, Kind P. Testing the validity of the EuroQoL and comparing it with the SF-36 health survey questionnaire. Qual Life Res 1993; 2: 169-180[Medline].
  12. Van Agt H, Essink-Bot M-L, Krabbe P, Bonsel G. Test-retest reliability of health state valuations collected with the EuroQoL questionnaire. Soc Sci Med 1994; 39: 1537-1544.
  13. Essink-Bot M-L, Krabbe P, Bonsel G, Aaronson N. An empirical comparison of four generic health status measures: the Nottingham health profile, the medical outcomes study 36-item short-form health survey, the COOP/WONCA charts, and the EuroQoL Instrument. Med Care 1997; 35: 522-537[Medline].
  14. Hurst NP, Jobanputra P, Hunter M, Lambert M, Lochead A, Brown H. Validity of EuroQoL---a generic health status instrument---in patients with rheumatoid arthritis. Br J Rheumatol 1994; 33: 655-662[Abstract/Free Full Text].
  15. Sculpher M, Dwyer N, Byford S, Stirrat G. Randomised trial comparing hysterectomy and transcervical endometrial resection: effect on health related quality of life and costs two years after surgery. Br J Obstet Gynaecol 1996; 103: 142-194[Medline].
  16. Hollingworth W, Mackenzie R, Todd CJ, Dixon AK. Measuring changes in quality of life following magnetic resonance imaging of the knee: SF-36, EuroQoL or Rosser index? Qual Life Res 1995; 4: 325-334[Medline].
  17. Erens B. Health-related quality of life: general population survey. London: Social and Community Planning Research , 1994(Technical report.)
  18. Kish L. Survey sampling. New York: Wiley , 1965.
  19. Thomas M, Goddard E, Hickman M, Hunter P. The general household survey 1992. London: HMSO , 1994(OPCS Series GHS No 23.)
  20. Martin J, Letzer H, Elliot D. The prevalence of disability among adults. OPCS surveys of disability in Great Britain. Report 1. London: HMSO, 1988. 
  21. Dolan P, Gudex C, Kind P, Williams A. A social tariff for EuroQoL: results from a UK general population survey. University of York: Centre for Health Economics , 1995(Discussion paper 138.)
  22. Department of Health and Social Security. Prevention and health: everybody's business. A reassessment of public and personal health. London: HMSO , 1976.
  23. Black D, Morris JN, Smith C, Townsend P. Black Report. Inequalities in health: report of a research working group. London: Department of Health and Social Security, 1980. 
  24. Rahkonen O, Arber S, Lahelma E. Health inequalities in early adulthood: a comparison of young men and women in Britain and Finland. Soc Sci Med 1995; 41: 163-171.
  25. In: Prescott-Clarke P, Primatesta P, eds. Health survey for England, 1996. London: Stationery Office , 1998.
  26. Weinstein MC, Siegel JE, Gold MR, Kamlet MS, Russell LB. Recommendations of the panel on cost-effectiveness in health and medicine. JAMA 1996; 276: 1253-1258[Abstract/Free Full Text].

(Accepted 31 October 1997)


© BMJ 1998

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to StumbleUpon StumbleUpon   Add to Technorati Technorati    What's this?

Relevant Articles

Helicobacter pylori test and treat versus proton pump inhibitor in initial management of dyspepsia in primary care: multicentre randomised controlled trial (MRC-CUBE trial)
Brendan C Delaney, Michelle Qume, Paul Moayyedi, Richard F A Logan, Alexander C Ford, Cathy Elliott, Cliodna McNulty, Sue Wilson, and F D Richard Hobbs
BMJ 2008 336: 651-654. [Abstract] [Full Text] [PDF]

Variations in population health status
Ann Bowling
BMJ 1998 317: 601. [Extract] [Full Text]

EuroQoL EQ-5D is a practical measure of population health
BMJ 1998 316: 0. [Full Text]

This article has been cited by other articles:

  • MERKEL, P. A., HERLYN, K., MAHR, A. D., NEOGI, T., SEO, P., WALSH, M., BOERS, M., LUQMANI, R. (2009). Progress Towards a Core Set of Outcome Measures in Small-vessel Vasculitis. Report from OMERACT 9. The Journal of Rheumatology 36: 2362-2368 [Abstract] [Full text]  
  • Rose, M. S., Koshman, M.-L., Ritchie, D., Sheldon, R. (2009). The development and preliminary validation of a scale measuring the impact of syncope on quality of life. Europace 11: 1369-1374 [Abstract] [Full text]  
  • Barton, G. R., Hodgekins, J., Mugford, M., Jones, P. B., Croudace, T., Fowler, D. (2009). Measuring the benefits of treatment for psychosis: validity and responsiveness of the EQ-5D. Br. J. Psychiatry 195: 170-177 [Abstract] [Full text]  
  • Sorensen, J., Davidsen, M., Gudex, C., Pedersen, K. M., Bronnum-Hansen, H. (2009). Danish EQ-5D population norms. Scand J Public Health 37: 467-474 [Abstract]  
  • Hildon, Z., Montgomery, S. M., Blane, D., Wiggins, R. D., Netuveli, G. (2009). Examining Resilience of Quality of Life in the Face of Health-Related and Psychosocial Adversity at Older Ages: What is "Right" About the Way We Age?. The Gerontologist 0: gnp067v1-gnp067 [Abstract] [Full text]  
  • Petrou, S., Kupek, E. (2009). Estimating Preference-Based Health Utilities Index Mark 3 Utility Scores for Childhood Conditions in England and Scotland. Med Decis Making 29: 291-303 [Abstract]  
  • Lekander, I., Borgstrom, F., Strom, O., Zethraeus, N., Kanis, J. A (2009). Cost-effectiveness of hormone replacement therapy for menopausal symptoms in the UK. Menopause Int 15: 19-25 [Abstract] [Full text]  
  • King, J. T. Jr, Tsevat, J., Roberts, M. S. (2009). Impact of the Scale Upper Anchor on Health State Preferences. Med Decis Making 29: 257-266 [Abstract]  
  • Wildman, M J, Sanderson, C F B, Groves, J, Reeves, B C, Ayres, J G, Harrison, D, Young, D, Rowan, K (2009). Survival and quality of life for patients with COPD or asthma admitted to intensive care in a UK multicentre cohort: the COPD and Asthma Outcome Study (CAOS). Thorax 64: 128-132 [Abstract] [Full text]  
  • Olivieri, I., de Portu, S., Salvarani, C., Cauli, A., Lubrano, E., Spadaro, A., Cantini, F., Cutro, M. S., Mathieu, A., Matucci-Cerinic, M., Pappone, N., Punzi, L., Scarpa, R., Mantovani, L. G., for the PACE working group, (2008). The psoriatic arthritis cost evaluation study: a cost-of-illness study on tumour necrosis factor inhibitors in psoriatic arthritis patients with inadequate response to conventional therapy. Rheumatology (Oxford) 47: 1664-1670 [Abstract] [Full text]  
  • Jia, H., Lubetkin, E. I. (2008). Estimating EuroQol EQ-5D Scores from Population Healthy Days Data. Med Decis Making 28: 491-499 [Abstract]  
  • Woodhall, S, Ramsey, T, Cai, C, Crouch, S, Jit, M, Birks, Y, Edmunds, W J, Newton, R, Lacey, C J N (2008). Estimation of the impact of genital warts on health-related quality of life. Sex. Transm. Infect. 84: 161-166 [Abstract] [Full text]  
  • Delaney, B. C, Qume, M., Moayyedi, P., Logan, R. F A, Ford, A. C, Elliott, C., McNulty, C., Wilson, S., Hobbs, F D R. (2008). Helicobacter pylori test and treat versus proton pump inhibitor in initial management of dyspepsia in primary care: multicentre randomised controlled trial (MRC-CUBE trial). BMJ 336: 651-654 [Abstract] [Full text]  
  • Lindgren, P, Buxton, M, Kahan, T, Poulter, N R, Dahlof, B, Sever, P S, Wedel, H, Jonsson, B, on behalf of the ASCOT trial investigators*, (2008). Economic evaluation of ASCOT-BPLA: antihypertensive treatment with an amlodipine-based regimen is cost effective compared with an atenolol-based regimen. Heart 94: e4-e4 [Abstract] [Full text]  
  • Lamotte, M., Annemans, L., Bridgewater, B., Kendall, S., Siebert, M. (2007). A health economic evaluation of concomitant surgical ablation for atrial fibrillation. Eur. J. Cardiothorac. Surg. 32: 702-710 [Abstract] [Full text]  
  • Culleton, B. F., Walsh, M., Klarenbach, S. W., Mortis, G., Scott-Douglas, N., Quinn, R. R., Tonelli, M., Donnelly, S., Friedrich, M. G., Kumar, A., Mahallati, H., Hemmelgarn, B. R., Manns, B. J. (2007). Effect of Frequent Nocturnal Hemodialysis vs Conventional Hemodialysis on Left Ventricular Mass and Quality of Life: A Randomized Controlled Trial. JAMA 298: 1291-1299 [Abstract] [Full text]  
  • Brennan, D.S., Spencer, A.J., Roberts-Thomson, K.F. (2007). Quality of Life and Disability Weights Associated with Periodontal Disease. JDR 86: 713-717 [Abstract] [Full text]  
  • The Adjuvant Breast Cancer Trials Collaborative Gr, (2007). Polychemotherapy for Early Breast Cancer: Results From the International Adjuvant Breast Cancer Chemotherapy Randomized Trial. JNCI J Natl Cancer Inst 99: 506-515 [Abstract] [Full text]  
  • Parry, G., Van Cleemput, P., Peters, J., Walters, S., Thomas, K., Cooper, C. (2007). Health status of Gypsies and Travellers in England. J. Epidemiol. Community Health 61: 198-204 [Abstract] [Full text]  
  • Lenzen, M. J, Scholte op Reimer, W. J M, Pedersen, S. S, Boersma, E., Maier, W., Widimsky, P., Simoons, M. L, Mercado, N. F, Wijns, W., on behalf of the investigators of the Euro Heart S, (2007). The additional value of patient-reported health status in predicting 1-year mortality after invasive coronary procedures: a report from the Euro Heart Survey on Coronary Revascularisation. Heart 93: 339-344 [Abstract] [Full text]  
  • van Staa, T. P., Geusens, P., Zhang, B., Leufkens, H. G. M., Boonen, A., Cooper, C. (2007). Individual fracture risk and the cost-effectiveness of bisphosphonates in patients using oral glucocorticoids. Rheumatology (Oxford) 46: 460-466 [Abstract] [Full text]  
  • Kobelt, G., Berg, J., Atherly, D., Hadjimichael, O. (2006). Costs and quality of life in multiple sclerosis: A cross-sectional study in the United States. Neurology 66: 1696-1702 [Abstract] [Full text]  
  • Liu, H., Michaud, K., Nayak, S., Karpf, D. B., Owens, D. K., Garber, A. M. (2006). The Cost-effectiveness of Therapy With Teriparatide and Alendronate in Women With Severe Osteoporosis.. Arch Intern Med 166: 1209-1217 [Abstract] [Full text]  
  • Nilsson, P. M., Nilsson, J.-A., Ostergren, P.-O., Berglund, G. (2005). Social mobility, marital status, and mortality risk in an adult life course perspective: The Malmo Preventive Project. Scand J Public Health 33: 412-423 [Abstract]  
  • Espallargues, M., Czoski-Murray, C. J., Bansback, N. J., Carlton, J., Lewis, G. M., Hughes, L. A., Brand, C. S., Brazier, J. E. (2005). The Impact of Age-Related Macular Degeneration on Health Status Utility Values. IOVS 46: 4016-4023 [Abstract] [Full text]  
  • Raman, R., Kamath, R. P., Parikh, A., Angus, P. D. (2005). Revision of cemented hip arthroplasty using a hydroxyapatite-ceramic-coated femoral component. J Bone Joint Surg Br 87-B: 1061-1067 [Abstract] [Full text]  
  • Cairney, J. (2005). Housing Tenure and Psychological Well-Being During Adolescence. Environment and Behavior 37: 552-564 [Abstract]  
  • Schousboe, J. T., Nyman, J. A., Kane, R. L., Ensrud, K. E. (2005). Cost-Effectiveness of Alendronate Therapy for Osteopenic Postmenopausal Women. ANN INTERN MED 142: 734-741 [Abstract] [Full text]  
  • Calvert, M. J., Freemantle, N., Cleland, J. G.F. (2005). The impact of chronic heart failure on health-related quality of life data acquired in the baseline phase of the CARE-HF study. Eur J Heart Fail 7: 243-251 [Abstract] [Full text]  
  • Paul, A, Lewis, M, Shadforth, M F, Croft, P R, van der Windt, D A W M, Hay, E M (2004). A comparison of four shoulder-specific questionnaires in primary care. Ann Rheum Dis 63: 1293-1299 [Abstract] [Full text]  
  • Franks, P., Lubetkin, E. I., Gold, M. R., Tancredi, D. J., Jia, H. (2004). Mapping the SF-12 to the EuroQol EQ-5D Index in a National US Sample. Med Decis Making 24: 247-254 [Abstract]  
  • Picavet, H S J, Hoeymans, N (2004). Health related quality of life in multiple musculoskeletal diseases: SF-36 and EQ-5D in the DMC3 study. Ann Rheum Dis 63: 723-729 [Abstract] [Full text]  
  • Ascione, R., Reeves, B. C., Taylor, F. C., Seehra, H. K., Angelini, G. D. (2004). Beating heart against cardioplegic arrest studies (BHACAS 1 and 2): quality of life at mid-term follow-up in two randomised controlled trials. Eur Heart J 25: 765-770 [Abstract] [Full text]  
  • Rome, K., Gray, J., Stewart, F., Hannant, S. C., Callaghan, D., Hubble, J. (2004). Evaluating the Clinical Effectiveness and Cost-effectiveness of Foot Orthoses in the Treatment of Plantar Heel Pain: A Feasibility Study. J. Am. Podiatr. Med. Assoc. 94: 229-238 [Abstract] [Full text]  
  • Asthana, S, Gibson, A, Moon, G, Brigham, P, Dicker, J (2004). The demographic and social class basis of inequality in self reported morbidity: an exploration using the Health Survey for England. J. Epidemiol. Community Health 58: 303-307 [Abstract] [Full text]  
  • Hol, M. K. S., Spath, M. A., Krabbe, P. F. M., van der Pouw, C. T. M., Snik, A. F. M., Cremers, C. W. R. J., Mylanus, E. A. M. (2004). The Bone-Anchored Hearing Aid: Quality-of-Life Assessment. Arch Otolaryngol Head Neck Surg 130: 394-399 [Abstract] [Full text]  
  • Pollack, C E, von dem Knesebeck, O, Siegrist, J (2004). Housing and health in Germany. J. Epidemiol. Community Health 58: 216-222 [Abstract] [Full text]  
  • Lawrence, W. F., Fleishman, J. A. (2004). Predicting EuroQoL EQ-5D Preference Scores from the SF-12 Health Survey in a Nationally Representative Sample. Med Decis Making 24: 160-169 [Abstract]  
  • Forouzanfar, T., Kemler, M. A., Weber, W. E. J., Kessels, A. G. H., van Kleef, M. (2004). Spinal cord stimulation in complex regional pain syndrome: cervical and lumbar devices are comparably effective. Br J Anaesth 92: 348-353 [Abstract] [Full text]  
  • Salomon, J. A, Tandon, A., Murray, C. J L (2004). Comparability of self rated health: cross sectional multi-country survey using anchoring vignettes. BMJ 328: 258- [Abstract] [Full text]  
  • Warren, E., Brennan, A., Akehurst, R. (2004). Cost-Effectiveness of Sibutramine in the Treatment of Obesity. Med Decis Making 24: 9-19 [Abstract]  
  • Kim Bao Giang, , Allebeck, P. (2003). Self-reported illness and use of health services in a rural district of Vietnam: findings from an epidemiological field laboratory. Scand J Public Health 31: 52-58 [Abstract]  
  • Gringeri, A., Mantovani, L. G., Scalone, L., Mannucci, P. M. (2003). Cost of care and quality of life for patients with hemophilia complicated by inhibitors: the COCIS Study Group. Blood 102: 2358-2363 [Abstract] [Full text]  
  • Segui-Gomez, M., MacKenzie, E. J. (2003). Measuring the Public Health Impact of Injuries. Epidemiol Rev 25: 3-19 [Full text]  
  • Nathoe, H. M., van Dijk, D., Jansen, E. W.L., Suyker, W. J.L., Diephuis, J. C., van Boven, W.-J., de la Riviere, A. B., Borst, C., Kalkman, C. J., Grobbee, D. E., Buskens, E., de Jaegere, P. P.T., the Study Group, (2003). A Comparison of On-Pump and Off-Pump Coronary Bypass Surgery in Low-Risk Patients. NEJM 348: 394-402 [Abstract] [Full text]  
  • Kim Bao Giang, , Allebeck, P. (2003). Self-reported illness and use of health services in a rural district of Vietnam: findings from an epidemiological field laboratory. Scand J Public Health 31: 52-58 [Abstract]  
  • Haywood, K. L., Garratt, A. M., Dziedzic, K., Dawes, P. T. (2002). Generic measures of health-related quality of life in ankylosing spondylitis: reliability, validity and responsiveness. Rheumatology (Oxford) 41: 1380-1387 [Abstract] [Full text]  
  • Carr, A., Workman, C., Smith, D. E., Hoy, J., Hudson, J., Doong, N., Martin, A., Amin, J., Freund, J., Law, M., Cooper, D. A., for the Mitochondrial Toxicity Study Group, (2002). Abacavir Substitution for Nucleoside Analogs in Patients With HIV Lipoatrophy: A Randomized Trial. JAMA 288: 207-215 [Abstract] [Full text]  
  • Redekop, W. K., Koopmanschap, M. A., Stolk, R. P., Rutten, G. E.H.M., Wolffenbuttel, B. H.R., Niessen, L. W. (2002). Health-Related Quality of Life and Treatment Satisfaction in Dutch Patients With Type 2 Diabetes. Diabetes Care 25: 458-463 [Abstract] [Full text]  
  • Ihlebaek, C., Eriksen, H. R., Ursin, H. (2002). Prevalence of subjective health complaints (SHC) in Norway. Scand J Public Health 30: 20-29 [Abstract]  
  • Saeed, I., Anyanwu, A. C., Yacoub, M. H., Amrani, M. (2001). Subjective patient outcomes following coronary artery bypass using the radial artery: results of a cross-sectional survey of harvest site complications and quality of life. Eur. J. Cardiothorac. Surg. 20: 1142-1146 [Abstract] [Full text]  
  • Badia, X., Roset, M., Herdman, M., Kind, P. (2001). A Comparison of United Kingdom and Spanish General Population Time Trade-off Values for EQ-5D Health States. Med Decis Making 21: 7-16 [Abstract]  
  • Kersnik, J. (2000). Observational study of home visits in Slovene general practice: patient characteristics, practice characteristics and health care utilization. Fam Pract 17: 389-393 [Abstract] [Full text]  
  • Schrag, A., Selai, C., Jahanshahi, M., Quinn, N. P (2000). The EQ-5D---a generic quality of life measure---is a useful instrument to measure quality of life in patients with Parkinson's disease. J. Neurol. Neurosurg. Psychiatry 69: 67-73 [Abstract] [Full text]  
  • Johnson, J. A., Ohinmaa, A., Murti, B., Sintonen, H., Coons, S. J. (2000). Comparison of Finnish and U.S.-based Visual Analog Scale Valuations of the EQ-5D Measure. Med Decis Making 20: 281-289 [Abstract]  
  • TREASURE, T. (1999). The measurement of health related quality of life. Heart 81: 331-332 [Full text]  
  • Bowling, A. (1998). Variations in population health status. BMJ 317: 601a-601 [Full text]  



Access jobs at BMJ Careers
Whats new online at Student 

BMJ