Issues

Volume 169 Issue 4

17 August 1998

Editorials Outcome measures of an Australian breast-screening program Alan Rodger, Anne M Kavanagh (MJA 1998; 169: 179-180)Use of complementary medicines: scientific and ethical issues Paul A Komesaroff (MJA 1998; 169: 180-181) Research Interval breast cancers in an Australian mammographic screening program Mary T Rickard, Richard J Taylor, Mohamed A Fazli, Nadima El Hassan (MJA 1998; 169: 184-187) Abstract - ArticleHelicobacter pylori infection: an added stressor on iron status of women in the community Hedley G Peach, Nicole E Bath, Stephen J Farish (MJA 1998; 169: 188-190)Psychological morbidity and quality of life in Australian women with early-stage breast cancer: a cross-sectional survey David W Kissane, David M Clarke, Jillian Ikin, Sidney Bloch, Graeme C Smith, Luis Vitetta, Dean P McKenzie (MJA 1998; 169: 192-196) Healthcare Acupuncture in Australian general practice: practitioner characteristics Gary Easthope, Justin J Beilby, Gerard F Gill, Bruce K Tranter (MJA 1998; 169: 197-200) Abstract - Article Notable Cases Cerebral histoplasmosis in an Australian patient with systemic lupus erythematosus Alice-Ann Sullivan, Susan M Benson, Arthur H Ewart, Patrick G Hogan, R Michael Whitby, Richard S Boyle (MJA 1998; 169: 201-202) Viewpoint The diastolic debate: is it time to discard Korotkoff phase IV in favour of phase V for blood pressure measurements in pregnancy? Susan P Walker, John R Higgins, Shaun P Brennecke (MJA 1998; 169: 203-205) New Drugs, Old Drugs Proton pump inhibitors Peter H Katelaris (MJA 1998; 169: 208-211) Medicine and the Law Breast cancer and malpractice litigation Allan O Langlands (MJA 1998; 169: 212-214) Clinical Practice Antenatal screening and prenatal diagnosis of thalassaemia: an update Kirsten A Small, Fung Yee Chan (MJA 1998; 169: 215-219) MJA Practice Essentials - Gastroenterology Diseases associated with Helicobacter pylori Anouk T Dev, John R Lambert (MJA 1998; 169: 220-225)

Editorials

Cancer 17 August 1998 Free

Outcome measures of an Australian breast-screening program

Outcome measures of an Australian breast-screening program One surrogate measure of the quality and effectiveness of screening MJA 1998; 169: 179-180 Mammographic screening for the early detection of breast cancer is a population-based measure for which randomised controlled trials have shown a 30% reduction in mortality in women aged between 50 and 69 years and who are screened.1 It is often forgotten that Australia is one of only a few countries where the State (in the form of both Federal and State governments) funds a national program of mammographic screening. From the outset of this program, there was an insistence that a quality service was essential if the predicted mortality reduction benefits were to be realised. Thus, national quality benchmarks based on international data were set. These were incorporated into accreditation standards to apply to all services in all States and Territories. This 30% mortality reduction depended on achieving a screening rate of approximately 70% of the target population, but it was recognised that even with 100% participation an inadequate, poor-quality service would not deliver the goods. The national screening program was phased in from 1992 and now covers the whole country. The accreditation standards are achievable, but screening participation has yet to reach target, and it will be several more years before mortality statistics for breast cancer can be affected by screening. Surrogate measures for the effectiveness of the service are therefore needed. One predictor of future breast cancer mortality is the small cancer detection rate, and it is gratifying that most States and Territories have already achieved the national accreditation standard.2 Another predictor of the effectiveness of the screening program is the interval cancer rate measured at State and national levels. The interval cancer rate is usually defined as the rate of diagnosis of new cases of invasive breast cancer and ductal carcinoma-in-situ in the two-year interval after a screening examination. In this issue of the Journal Rickard et al report rates and proportional incidences of interval cancers in the 12 months after screening from a New South Wales pilot mammographic screening program.3 The proportional incidence is the proportion that interval invasive breast cancers comprise of the total number of invasive breast cancers expected in the absence of screening. While the proportional incidence reported by Rickard et al is lower than that reported in studies from the United Kingdom4 and the Netherlands,5 it is higher than that found in the Swedish Two-County Study.6 As the confidence intervals found in all these studies overlap, we cannot conclude that these differences are statistically significant. However, the lack of a statistically significant difference in the proportional incidence between the study by Rickard and colleagues3 and the Swedish one6 cannot be taken to mean that they will achieve a similar mortality reduction. Larger State-based and national studies are needed to make international comparisons. The 12-month interval-cancer incidence of 4.17 per 10 000 screens in the women aged 40-49 years and 4.64 per 10 000 screens in women aged 50-69 reported by Rickard et al3 are lower than that reported by the South Australian screening program.7 However, because the confidence intervals for the New South Wales rate3 include the SA estimate, these differences are not statistically significant. To calculate rates and proportional incidences of interval cancers, we need well-functioning, complete and up-to-date BreastScreen services and cancer registries in each of the States and Territories. This requires both political will and financial resources, at national and State levels. It is also essential that each program counts interval cancers in the same way. In the UK,8 different definitions of interval cancers gave estimates of the interval cancer rate which varied by nearly 30%. While the low 12-month incidence rate found by Rickard et al is promising, it is also important to measure this in the second year after screening, when interval cancers are likely to form a greater proportion of the expected incidence of breast cancer. Also, although this study is too small to present separate interval cancer rates for the first and second screening round, future studies must do this, as these rates may differ. Nevertheless, it is essential to recognise the need to measure interval cancer rates in breast screening in a consistent fashion, in each State and Territory as well as nationally. Although interval cancers are inevitable, they are a measure of the sensitivity of a program whose object is to ensure that a high proportion of women with cancer are diagnosed by the screening process. However, achieving the lowest possible interval cancer rate must not be done at the expense (financial and emotional) of recalling a high proportion of women for further assessment that would lead to high rates of false positives (as happened in one American service where one-third of women without cancer received an abnormal screening result over 10 years).9 BreastScreen Australia is just over five years old and in its infancy. It has attained a high level of awareness among women,10 with very high levels of acceptability as shown by high rescreening levels.11 Government funding permits a quality of screening not available in the world's first national program, in the United Kingdom -- double-view mammography, double specialist reading and a two-yearly screening interval. To ensure quality and to assess whether their stewardship of this national investment in women's health is likely to have produced the expected reduction in breast cancer mortality, programs should be encouraged not only to attain the accreditation standards, but also to use nationally agreed surrogate measures for overall mortality changes, of which interval cancer rates are but one. Further, governments must support their investment by encouraging and funding the collection and interchange of these nationally agreed data. Alan Rodger Professor and Director The William Buckland Radiotherapy Centre, The Alfred Health Care Group, Melbourne, VIC Anne M Kavanagh Public Health Research Fellow Cancer Epidemiology Centre, Anti Cancer Council of Victoria, Melbourne, VIC Hurley SF, Kaldor JM. The benefits and risks of mammographic screening for breast cancer. Epidemiol Rev 1992; 14: 101-103. National Program for the Early Detection of Breast Cancer -- national accreditation requirements: March 1994. Canberra: Commonwealth Department of Human Services and Health, December 1994. Rickard MT, Taylor R, Fazli MA, El Hassan N. Interval breast cancers in an Australian mammographic screening programme. Med J Aust 1998; 169: 184-187. Woodman CBJ, Threlfall AG, Boggis CRM, Prior P. Is the three year breast screening interval too long? Occurrence of interval cancers in NHS breast screening programme's north western region. BMJ 1995; 310: 224-226. Peeters PHM, Verbeek ALM, Hendricks JHCL, et al. The occurrence of interval cancers in the Nijmegen screening programme. Br J Cancer 1989; 59: 929-932. Tabar L, Faberberg G, Day NE, Holmberg L. What is the optimum interval between mammographic screening examinations? An analysis on the latest results of the Swedish two-county breast cancer screening trial. Br J Cancer 1987; 55: 547-551. Robinson JL, Crane CEB, King JM, et al. The South Australian breast x-ray service: results from a statewide mammographic screening programme. Br J Cancer 1996; 73: 837-842. Faux AM, Richardson DC, Lawrence GM, et al. Interval breast cancers in the NHS breast screening programme: does the current definition exclude too many? J Med Screening 1997; 4: 169-173. Elmore JG, Barton MB, Moceri VM, et al. Ten-year risk of false positive screening mammograms and clinical breast examination. N Engl J Med 1998; 338: 1089-1096. Barratt AL, Cockburn J, Redman S, Perkins PC. Mammographic screening: results from the 1996 National Breast Health Survey. Med J Aust 1997; 167: 521-524. BreastScreen Victoria. Annual Statistical Report 1996. Melbourne: Victorian Breast Screening Co-ordination Unit Inc., 1996: 12. - Readers may print a single copy for personal use. No further reproduction or distribution of the articles should proceed without the permission of the publisher. For permission, contact the Australasian Medical Publishing Company Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au>". <URL: http://www.mja.com.au/>

Alan Rodger · Anne M Kavanagh

Complementary therapies 17 August 1998 Free

Use of complementary medicines: scientific and ethical issues

Use of complementary medicines: scientific and ethical issues We need to address questions of effectiveness, safety and regulation MJA 1998; 169: 180-181 This article has been cited in Rey JM, Walter G. Hypericum perforatum (St John's wort) in depression: pest or blessing? MJA 1998; 169: 583-586. The widespread acceptance of complementary medicines in Australia raises important scientific, social and ethical issues. The expression "complementary medicines" covers a diverse range of practices, from historically well-established therapies, such as traditional Chinese medicine, to more exotic forms, such as colour therapy and psychic healing.1 Taken together, the precise extent of their use is unknown. Certainly, the industry is a very large one: in the United States and Australia about one-fifth of the population visit alternative practitioners each year, and in Australia up to half the population have visited them at some stage.2-4 In the United States, expenditure on complementary therapies in 1990 was about $14 billion;3 for Australia, precise data are not available, but the figure is likely to be in the hundreds of millions of dollars.2,4 The use of complementary medicines is increasing. Again, data are scanty. However, over the last five years the number of raw medicinal substances imported for use in Australia has increased fourfold, and there are now about 300-400 individual medicines available.5 Since the introduction of a Medicare rebate for acupuncture in 1984, use of acupuncture by medical practitioners has increased greatly. By analysing one of the few reliable sources of data available, Health Insurance Commission records, Easthope et al,6 in this issue of the Journal, show that the number of Medicare claims for acupuncture services by general practitioners grew by nearly 50% in 12 years, to almost one million in 1996-97. Medicare reimbursements to doctors for acupuncture increased during this period from $7.7 million to $17.7 million, and in 1996 about 15% of general practitioners presented Medicare claims for acupuncture. Evidence regarding the clinical effectiveness of most complementary treatments, and the risks associated with them, is extremely limited.7,8 Randomised clinical trials have been few; indeed, it has been argued that complementary therapies in general, and traditional Chinese practices in particular, are in principle not susceptible to assessment using randomised-trial designs.7 In the case of acupuncture, significant insights have been achieved into physiological mechanisms of action; however, the few clinical studies that have been performed have often been flawed by poor design, inadequate measures and statistical analysis, and lack of follow-up data.7,8 Notwithstanding this, rigorous trials are possible, as has been shown by studies that support the use of acupuncture in the treatment of pain and nausea, and suggest possible applications in other areas, such as hypertension and asthma.7,8 It is important to recognise that complementary medicines, like orthodox ones, are not without risk. There is the possibility that use of complementary treatments might lead to withdrawal from appropriate medical therapy or to delays in diagnosis or treatment of underlying conditions. In addition, physical treatments can cause adverse effects, and herbal therapies can be either intrinsically toxic or contaminated with toxic substances. As recent discussions in the Journal have highlighted, serious reactions and even death can occur.8-11 Complications of acupuncture have included pneumothorax and puncture of other vital organs, spinal cord lesions, and infections (including HIV and hepatitis B),12,13 again associated with possible death.14 A National Health and Medical Research Council working party in 1989 found that complications occurred most frequently with acupuncturists without medical training.14 The widespread use of complementary medicines, and especially the application of acupuncture by general practitioners demonstrated by Easthope et al, raises some interesting social and ethical questions: It is widely accepted that individuals should be free to make their own choices with respect to healthcare; however, are not claims of cures matters of public interest affecting public health? Should the application of public funds be directed by consumer demand, or should it be limited to practices -- orthodox or complementary -- for which reasonable evidence of effectiveness and safety can be provided? Should the training and right to practise of complementary therapists -- at present largely unrestricted -- be subject to a formal system of regulation? Does the community have an obligation to protect vulnerable citizens from exploitation by practitioners holding uncertain qualifications, who apply practices with dubious benefits and unknown risks? Should special measures be introduced to protect children, especially from practices that may lead to their being denied conventional therapies of proven efficacy?15 Why have risk and lack of evidence not deterred potential patients and practitioners? The question of why people use complementary therapies is an important one which may have ethical implications of its own. There is evidence that people turn to alternatives because they are disillusioned with orthodox medicine. This may include dissatisfaction with doctor-patient interactions or dissatisfaction with medicine in general.16 Declining public support for hospitals and the introduction of economic practices such as managed care, which promote cost-saving at the risk of reducing the quality of service, may well exacerbate this process. Some form of regulation of complementary medicines seems to be necessary, but a delicate balance needs to be struck between control and consumer choice. A possible model, referred to as "protection of title", is presently under consideration in Victoria, following a government-sponsored inquiry into the practice of traditional Chinese medicine. It is believed that legislation will be introduced to limit the use of the titles "acupuncturist" and "practitioner of traditional Chinese medicine" to individuals who have been accredited by specified registration bodies. This approach would contribute to the establishment of standards of practice and training and provide avenues for aggrieved consumers to have their complaints addressed. Unregistered therapists could continue to practise as long as they did not claim to hold specific qualifications to do so. It is quite likely that some form of protection of title will eventually be adopted as a general approach to the regulation of various forms of complementary therapy throughout Australia. This approach, however, represents only a partial solution. It will still be necessary to consider whether therapies work and are safe -- and, indeed, whether this question can be answered at all. It will still be necessary for us to understand the cultural meaning of complementary medicines and what they have to teach orthodox practitioners. For these questions to be addressed, detailed research will be needed into not just the scientific but also the sociological, ethical and philosophical aspects of complementary medicines. It is to be hoped that such research will be undertaken, and that it will promote much-needed dialogue between practitioners of orthodox and complementary medicine. Paul A Komesaroff Associate Professor, Department of Medicine, Monash University and Director, Eleanor Shaw Centre for the Study of Medicine Society and Law Baker Medical Research Institute, Melbourne, VIC Eagle R. Alternative medicine. London: Futura, 1978. MacLennan AH, Wilson DH, Taylor AW. Prevalence and cost of alternative medicine in Australia. Lancet 1996; 347: 569-573. Eisenberg DM, Kessler RC, Foster C, et al. Unconventional medicine in the United States: prevalence, costs and patterns of use. N Engl J Med 1993; 328: 246-252. Ban E. Australian alternatives. Nat Med 1998; 4: 8. Myers S, Bensoussan A. Towards a safer choice: the practice of Chinese medicine in Australia. Sydney: Faculty of Health, University of Western Sydney, Macarthur, 1996. Easthope G, Beilby JJ, Gill GF, Tranter BK. Acupuncture in Australian general practice: practitioner characteristics. Med J Aust 1998; 169: 195-198. Vincent C, Furnham A. Complementary medicine: a research perspective. London: Wiley, 1997; 181-182. National Institutes of Health. Acupuncture. NIH Consensus Statement, April 1998. Mullins RJ. Echinacea-associated anaphylaxis. Med J Aust 1998; 168: 170-171. Kelly S. Aconite poisoning [letter]. Med J Aust 1990; 153: 499. Drew AK, Myers SP. Safety issues in herbal medicine: implications for the health professions. Med J Aust 1997; 166: 538-541. Halvorsen TB, Anda SS, Naess AB, Levang OW. Fatal cardiac tamponade after acupuncture through congenital sternal foramen [letter]. Lancet 1996; 345: 1175. Norheim AJ, Fønnebø V. Adverse effects of acupuncture [letter]. Lancet 1995; 345: 1576. National Health and Medical Research Council, Acupuncture Working Party. Acupuncture. Canberra: NHMRC, 1989. Neeley GS. Legal and ethical dilemmas surrounding prayer as a method of alternative healing for children. In: Humber JM, Almeder RF, editors. Alternative medicine and ethics. New Jersey: Humana Press, 1998; 163-194. Siahpush M. Postmodern values, dissatisfaction with conventional medicine and popularity of alternative therapies. J Sociology 1998; 34: 58-70. - Readers may print a single copy for personal use. No further reproduction or distribution of the articles should proceed without the permission of the publisher. For permission, contact the Australasian Medical Publishing Company Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au>". <URL: http://www.mja.com.au/>

Paul A Komesaroff

17 August 1998 Free

Spina bifida

Spina bifida We can reduce the incidence of this congenital defect with folate fortification of food MJA 1998; 169: 182-183 Each year about 80 babies in Australia are born with spina bifida, a congenital malformation. Spina bifida, including meningocele and meningomyelocele, is one of the spectrum of birth defects known as neural tube defects (NTDs). These defects result from failure of the neural tube to close normally during the first five weeks of embryonic life. The severity of the defect depends on where it occurs and whether nervous tissue or only meninges are involved. At least 80% of people with spina bifida have an Arnold-Chiari malformation and associated hydrocephalus, often requiring a ventricular shunt. Other chronic problems include impaired mobility, bladder and bowel dysfunction, and scoliosis, all of which contribute to high medical and psychosocial morbidity. The incidence of NTDs varies considerably according to geography and ethnicity, ranging from 0.8 to more than 10 per 1000 live births. The incidence in Australia is currently 1.1 per 1000 live births.1 Recurrence risks, which are dependent on the background incidence, reflect this variation. In Australia the recurrence risk for a couple with a previous NTD-affected pregnancy is 3%-4%, and the risk for any first-degree relatives is 1%.2 About 10% of NTDs are caused by chromosomal anomalies, predominantly trisomy 18 and triploidy, or by single-gene disorders. Maternal factors, including diabetes mellitus and exposure to the anticonvulsants valproic acid and carbamazepine, also predispose to NTDs.3 However, most NTDs are isolated malformations and are thought to be multifactorial in origin, caused by an interaction between a genetic predisposition and environmental factors.4 The B group vitamins folic acid (folate) and vitamin B12 appear to be involved in NTDs. These vitamins share metabolic pathways involved in DNA synthesis (Figure), so that a deficiency or metabolic derangement affecting either vitamin may result in impaired cell proliferation and an increased risk of congenital defects. The underlying biology is complex -- several studies have shown that women with NTD-affected pregnancies do not have folate and vitamin B12 levels in the defined deficiency ranges, although some have abnormalities such as hyperhomocysteinaemia, which suggest subtle metabolic defects.5,6 One important genetic influence may be a mutation in the gene for 5,10-methylenetetrahydrofolate reductase, an enzyme involved in folate metabolism (Figure). About 12% of the Caucasian population is homozygous for a mutation which produces a heat-labile form of this enzyme with reduced activity and higher folate requirements.7 This causes higher serum homocysteine levels, and is associated with a greater risk of NTD-affected pregnancies.8 NTDs can be prevented by reducing the incidence in all pregnancies (primary prevention), or by termination of affected pregnancies (secondary prevention). In Australia the rate of spina bifida in live births declined gradually from 7.1 per 10 000 births in 1987 to 2.9 per 10 000 births in 1994. During the same period the number of induced abortions carried out before 20 weeks' gestation for spina bifida increased, although notification of these therapeutic abortions was incomplete.1 These figures indicate that secondary prevention of NTDs is occurring throughout Australia, largely because of improvements in antenatal diagnosis. Antenatal diagnosis of NTDs usually involves maternal serum alpha-fetoprotein (MSAFP) estimation at 15-17 weeks' gestation (raised in NTD-affected pregnancies), followed by targeted ultrasound scanning at 18-19 weeks' gestation.9 The combined sensitivity of these two investigations is greater than 90%. Women at increased risk of an NTD-affected pregnancy may be offered first-trimester vaginal ultrasound and amniotic fluid alpha-fetoprotein and acetylcholinesterase estimation. Alpha-fetoprotein is raised, and acetylcholinesterase detectable, in NTD-affected pregnancies.10 Primary prevention of NTDs is preferable to secondary prevention. Although the mechanisms are not entirely understood, it is well established that periconceptional supplementation with folic acid plays a role in reducing by more than 70% the risk of both the first occurrence11 and the recurrence of NTDs.12 Therefore, current recommendations are that women planning a pregnancy should supplement their diets with 0.5 mg (500 µg) of folic acid daily, starting from at least one month before conception and continuing for the first 12 weeks of pregnancy. Women at increased risk of an NTD-affected pregnancy, including those with a previous NTD-affected pregnancy or a close family history of NTDs, should supplement their diet with 5 mg of folic acid daily.13,14 Despite apparent acceptance of the need for folic acid and the realisation that many Western women do not consume sufficient dietary folate, there has been relatively poor compliance with regimens of periconceptional folic acid supplementation.15,16 One of the main reasons is that at least half of all pregnancies are unplanned. Another reason is that some people cannot afford a folate-rich diet and others are unaware of what constitutes such a diet. There are also indications that obstetricians and general practitioners do not adequately educate and counsel their female patients of reproductive age about the need for periconceptional folic acid supplementation.17 Although education of women and their physicians to ensure consumption of folate-rich foods (such as green leafy vegetables) must continue, the relatively simple and inexpensive strategy of fortification of cereals, breads, pasta and milk would be more efficacious, as it does not involve specific planning or significant alteration of a woman's normal lifestyle or behaviour. This strategy is being applied in the United States -- in January 1998 the Food and Drug Administration, after considerable debate, made fortification of cereals with folic acid mandatory. In Australia, unfortunately, the National Health and Medical Research Council's Food Fortification Panel recommended only voluntary fortification, pending future review.18 Australian companies have not acted; the only folate-fortified breakfast cereals available in Australia are marketed by an American company. Let us hope that local companies will develop the vision to play a role in public health, and adopt voluntary food fortification policies. Debra S Kennedy Staff Specialist in Clinical Genetics Royal Prince Alfred Hospital, Sydney, NSW References Lancaster P, Hurst T, Day P, et al. Congenital Malformations Australia 1993 and 1994. Australian Institute of Health and Welfare National Perinatal Statistics Unit. Birth Defects Series, Number 2, 1997. Harper PS. Practical genetic counselling. 4th ed. Oxford: Butterworth-Heinemann, 1993; 177. Holmes LB. Spina bifida: anticonvulsants and other maternal influences. Ciba Found Symp 1994; 181: 232-238. Hall JG, Friedman JM, Kenna BA, et al. Clinical, genetic, and epidemiological factors in neural tube defects. Am J Hum Genet 1988; 43: 827-837. Mills JL, McPartlin JM, Kirke PN, et al. Homocysteine metabolism in pregnancies complicated by neural-tube defects. Lancet 1995; 345: 149-151. Kirke PN, Molloy AM, et al. Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects. Q J Med 1993; 86: 703-708. Wilcken DEL. MTHFR 677C®T mutation, folate intake, neural tube defect, and cardiovascular risk [commentary]. Lancet 1997; 350: 603-604. van der Put NMJ, Steegers-Theunissen RPM, Frosst P, et al. Mutated methylene tetrahydrofolate reductase as a risk for spina bifida. Lancet 1995; 346: 1071-1072. Nodel AS, Green NK, Holmes LB, et al. Absence of need for amniocentesis in patients with elevated levels of maternal serum alpha fetoprotein and normal ultrasonographic examinations. N Engl J Med 1990; 323: 557-561. Wald N, Cuckle M, Nanchahal K. Amniotic fluid acetylcholinesterase measurement in the prenatal diagnosis of open neural tube defects. Second report of the Collaborative Acetylcholinesterase Study. Prenat Diagn 1989; 9: 813-829. Czeizel AE, Dudas I. Prevention of the first occurrence on neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 1992; 327: 1832-1835. Medical Research Council Vitamin Study Research Group. Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. Lancet 1991; 338: 131-137. National Health and Medical Research Council. Revised statement on the relationship between dietary folic acid and neural tube defects such as spina bifida. Canberra: NHMRC, 1993. From the Centers for Disease Control and Prevention: recommendations for use of folic acid to reduce the number of spina bifida cases and other neural tube defects. JAMA 1993; 269: 1233-1238. Clark NA, Fisk NM. Minimal compliance with the Department of Health recommendation for routine prophylaxis to prevent fetal neural tube defects. Br J Obstet Gynaecol 1994; 101: 709-710. Marsack CR, Alsop CL, Kurinczuk JJ, Bower C. Pre-pregnancy counselling for the primary prevention of birth defects: rubella vaccination and folate intake. Med J Aust 1995; 162: 403-406. Perelman V, Singal N, Einarson A, et al. Knowledge and practice by Canadian family physicians regarding periconceptional folic acid supplementation for the prevention of neural tube defects. Can J Clin Pharmacol 1996; 3: 145-148. National Health and Medical Research Council. Report of the expert panel on folate fortification. Canberra: NHMRC, 1994. - Readers may print a single copy for personal use. No further reproduction or distribution of the articles should proceed without the permission of the publisher. For permission, contact the Australasian Medical Publishing Company Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au>". <URL: http://www.mja.com.au/>

Debra S Kennedy

Research

Cancer 17 August 1998 Free

Interval breast cancers in an Australian mammographic screening program

Interval breast cancers in an Australian mammographic screening program Mary T Rickard, Richard J Taylor, Mohamed A Fazli and Nadima El Hassan MJA 1998; 169: 184-187 For editorial comment, see Rodger & Kavanagh Abstract - Introduction - Methods - Results - Discussion - Acknowledgements - References - Authors' details - - ©MJA1998 Abstract Objective: To determine the incidence of interval cancers which occurred in the first 12 months after mammographic screening at a mammographic screening service. Design: Retrospective analysis of data obtained by crossmatching the screening Service and the New South Wales Central Cancer Registry databases. Setting: The Central & Eastern Sydney Service of BreastScreen NSW. Participants: Women aged 40-69 years at first screen, who attended for their first or second screen between 1 March 1988 and 31 December 1992. Main outcome measures: Interval-cancer rates per 10 000 screens and as a proportion of the underlying incidence of breast cancer (as estimated by the underlying rate in the total NSW population). Results: The 12-month interval-cancer incidence per 10 000 screens was 4.17 for the 40-49 years age group (95% confidence interval [CI], 1.35-9.73) and 4.64 for the 50-69 years age group (95% CI, 2.47-7.94). Proportional incidence rates were 30.1% for the 40-49 years age group (95% CI, 9.8-70.3) and 22% for the 50-69 years age group (95% CI, 11.7-37.7). There was no significant difference between the proportional incidence rate for the 50-69 years age group for the Central & Eastern Sydney Service and those of major successful overseas screening trials. Conclusion: Screening quality was acceptable and should result in a significant mortality reduction in the screened population. Given the small number of cancers involved, comparison of interval-cancer statistics of mammographic screening programs with trials requires age-specific or age-adjusted data, and consideration of confidence intervals of both program and trial data. Introduction The principal aim of a mammographic screening service is to reduce mortality from breast cancer. As this outcome cannot be measured effectively for many years after the establishment of screening, and as it applies to spatially defined populations, a range of interim measures are used to evaluate screening services and to determine the likelihood of mortality reduction. Interim measures include screen-detected cancer rates and the rates of prognostic indicators for these cancers, such as size, nodal status and grade.1 Another interim measure of screening performance is the interval-cancer rate.2,3 As survival among women with interval cancers is similar to that among unscreened women, then as the incidence of interval cancers approaches that of the underlying incidence of breast cancer the benefit of screening disappears.3 Interval-cancer rates can be compared with background or underlying rates to better assess the effectiveness of screening. Further, comparing the rate of interval cancers with the underlying rate allows comparison between different screening programs in populations with different incidences of breast cancer. Our aim was to evaluate first-year interval breast cancers after screening at the Central & Eastern Sydney Service of BreastScreen NSW (a mammographic screening and assessment service). We report the incidence and proportional incidence of interval breast cancers during the 12 months after both the first and second rounds of screening, over five years. Methods The Central & Eastern Sydney Service of BreastScreen NSW is located in inner Sydney, and started screening in March 1988 as one of the first pilot mammography screening programs in Australia. Any woman aged 40 years or more was eligible to attend, although during the study period only 50-69-year-old residents in the Central Sydney Area Health Service were actively recruited for two-yearly screening. Since the progressive introduction of systematic, government-funded, population-based screening from 1991, the Service has become a regional component of BreastScreen NSW and BreastScreen Australia.4The study population comprised women who attended the Service for mammographic screening between 1 March 1988 and 31 December 1992. These women were all screened by two-view mammography. The technical quality of the Service's screening mammograms met all requirements for accreditation by BreastScreen Australia.5 All films were read independently by two radiologists and were reported as "normal" for routine rescreen or as "suspicious" and requiring assessment. The design of the screening and assessment Service has been previously described.6 Screen-detected cancers The definition of primary breast cancer used for this study includes invasive cancer and ductal carcinoma-in-situ (DCIS), but excludes lobular carcinoma-in-situ.5 All cases of primary breast cancer diagnosed by the screening and assessment Service in women attending for the first time were classified as prevalent (first-round) screen-detected cancers. Cancers in women attending for their first routine rescreen after two years were classified as second-round screen-detected cancers. Data were analysed according to age at first screen, by 10-year age groups (40-49, 50-59 and 60-69 years). Interval cancers We reviewed the data for interval cancers, defined as primary cancer of the breast diagnosed up to 12 months after a first-round or second-round screening mammogram in women aged 40-69 years at the time of screening. The date of diagnosis of these interval cancers was taken as the date of histological confirmation of cancer. Cases in which clinical and imaging findings were consistent with breast cancer but no surgery had been performed were included in the study and the date of diagnosis was taken as the date of cytological confirmation of cancer. Data were analysed by women's age at their first screen. Some interval cancers were reported to the screening Service and others were identified by linking the Service's screening database with the NSW Central Cancer Registry (NSW CCR), which has operated since 1972 as a population-based registry. Notification of malignant neoplasms has been a statutory requirement for all NSW public and private hospitals, radiotherapy departments and nursing homes since 1972, and for pathology and outpatient departments since 1985. The date of diagnosis used by the NSW CCR was defined as "date of first definitive treatment for cancer" during the period covered by this study, although incidence was designated mostly on the basis of the first notification (usually the biopsy report). We matched records of the screening database with the NSW CCR in late 1994 with the aid of probabilistic linkage7,8 using Automatch.9 Equivocal matches were investigated by individual examination of all details available, and by active follow-up by the screening Service. Positive linkages between the screening database and the cancer registry were investigated by the screening Service to ensure that all data on those interval cancers diagnosed in the first year after a negative screen were available for inclusion in the study. Statistical analysis The age-specific incidence of interval cancers was determined by dividing the number of interval cancers found in women screened between 1988 and 1992 by the age-specific (age at first screen) number of women screened over the same period. Age groups were 40-49, 50-59 and 60-69 years, although the latter two age groups are aggregated for reporting purposes. The underlying incidence of breast cancer from 1988 to 1992 was obtained by dividing NSW reported cases (as reported by the NSW CCR.10,11) by the State female population for the same three 10-year age groups. To express the interval-cancer incidence as a proportion of the underlying breast cancer incidence rate, an indirectly age-standardised incidence ratio12 was calculated using the State age-specific incidences as the standard. Because of small numbers of cases, 95% confidence intervals were derived by the Poisson method.12,13We compared our findings with those of studies from Sweden,3 the Netherlands14 and the United Kingdom15 using the 12-month interval-cancer data from the first two screening rounds for all studies except the UK study, for which only the first-round data were available. Confidence limits for interval-cancer rates from comparison populations were calculated from the published data using the same Poisson method as above. Results During the study period, the Central & Eastern Sydney Service carried out 39 988 first-round and second-round screens on women aged 40-69 years, and 226 screen-detected cancers were diagnosed. In the prevalent (first-round) screens, the screen-detected cancer rates per 1000 screens were 3.0 for women aged 40-49 years, 6.2 for 50-59-year-olds and 9.6 for 60-69-year-olds. Second-round rates were 3.5, 4.2 and 4.6, respectively. Eighteen interval cancers occurred in the first 12 months after screening. All of these interval cancers were invasive. The 12-month interval-cancer incidences are shown in Box 1. The underlying annual breast cancer incidences were 13.8 per 10 000 for the 40-49 years age group and 21.2 per 10 000 for the 50-69 years age group (19.4 for 50-59 years and 23.2 for 60-69 years). The interval-cancer incidences as a proportion of these underlying incidences are shown in Box 2, in which they are compared with those of the Swedish Two-County Study.3 The proportional interval-cancer incidence for women aged 50-69 years in the Central & Eastern Sydney Service (22.0%; 95% CI, 11.7%-37.7%) is compared with that for similar age groups from international studies3,14,15 in Box 3. The proportional interval-cancer incidence point estimate for the Central & Eastern Sydney Service was higher and had wider 95% confidence intervals than that of the Swedish Two-County Study (13.2%; 95% CI, 8.4-19.9), but was lower than that of the UK (31.4%; 95% CI, 24.9-39.1) and Dutch (39.5%; 95% CI, 20.4-69.0) studies. Discussion The screen-detected cancer rates achieved by the Central & Eastern Sydney Service exceed the National Accreditation Requirements and compare favourably with those reported from the Swedish Two-County Study and the other Australian mammographic screening services.5,16,17Our findings indicate that the first 12-month interval-cancer rate (as a proportion of underlying incidence) for women attending the Central & Eastern Sydney Service is higher than that of the Swedish Two-County Study,3 but lower than the rates reported from Nijmegen (the Netherlands)14 and North West Region UK.15 However, there is considerable overlap of 95% confidence intervals, and the conclusion must be that the Central & Eastern Sydney proportional first-year interval-cancer rate is not significantly different from that in these other studies. As a proportion of interval cancers occur because an abnormality has not been detected at the time of screening, the first-year interval-cancer rates reflect the proportion of false negative screens in the screening episode. The Central & Eastern Sydney results therefore indicate acceptable screening sensitivity and, as they are not significantly different from the results of the Two-County Study, they would be expected to indicate a similar future mortality reduction. The interval-cancer data presented in this study are not affected by significant ascertainment bias. Restricting our analysis to interval cancers occurring within the first year after a screen eliminates the difficulties of accurately differentiating interval cancers and screen-detected cancers diagnosed around the 21-27-month rescreen interval. We directed considerable attention to the linkage with the NSW CCR to ensure that no interval cancers were missed. The underlying rate of breast cancer is reliable. This was determined in a population that included the women who were screened. However, during the study period, the Central & Eastern Sydney BreastScreen Service was one of only two pilot mammographic screening and assessment endeavours in New South Wales, and screened a small fraction of the State's female population. Its clientele was not limited to the immediate geographic area. For the busiest years in this period (1991 and 1992) less than 5% of breast cancers in NSW were detected through these two mammographic screening services.18 Completeness of enumeration is difficult to determine precisely for cancer registries, but the standard indicators suggest reasonably good completeness for the NSW CCR,10,19 and its data are accepted for inclusion in Cancer incidence in five continents.20 Comparisons of the Central & Eastern Sydney Service and another pilot mammographic screening service with the NSW CCR for the period 1988-1992 showed 100% enumeration of invasive breast cancer by the NSW CCR (R T, NSW Cancer Council, unpublished data). The design of the Australian mammographic screening program and the comparison studies in this paper differ. The Swedish Two-County Study employed single-view mammography and double reading. The Dutch and UK studies used single-view mammography and single reading. Double-view mammography and double reading, as used in Australia, would be expected to produce better results and fewer interval cancers in the first year than the comparison studies. The confidence intervals of the proportional interval-cancer rates from the Swedish Two-County Study and those reported for North West Region UK do not overlap, and direct statistical testing has shown a significant difference between these rates.15 The authors of the UK article15 and those of the accompanying editorial21 expressed concern that the screening sensitivity in the British National Health Service program may not be sufficient to achieve mortality reduction targets. They noted the increased sensitivity resulting from two-view mammography, good film quality and two independent film readings. These features are part of BreastScreen Australia and of the Central & Eastern Sydney Service. Even when data are collected over reasonable lengths of time, the numbers of interval cancers in many screening services are often small because of the size of the base populations. In the 50-69 years age group, there were 23 interval cancers in the Swedish Two-County Study, compared with 12 in the Nijmegen study and 13 in our study. However, performance can still be evaluated through calculation of interval-cancer rates, provided that interpretation is qualified by consideration of confidence intervals based on exact or Poisson methods. Australian mammography screening services are evaluated by comparison with National Accreditation Requirements standards.5 The point estimate of the Swedish Two-County Study has come to be regarded as a standard, as this study achieved significant mortality reduction. However the Two-County Study did not involve large numbers, and its interval-cancer rates must be interpreted in relation to their statistical confidence intervals. That is, standards cannot be derived from point estimates alone as they emanate from real studies in real populations. Further, comparison of the performance of screening services with such standards also requires that the confidence intervals of the screening service data be taken into account. Evaluations should not be based on point estimates of rates which derive from small numbers with considerable stochastic variation. The standard for Australian National Accreditation Requirements is less than six interval cancers per 10 000 screens occurring in the first 12 months. However, no age range or standardisation is specified, and confidence intervals are not considered. Another consideration in setting performance standards for mammographic screening services is the difference in results from experimental and operational studies. Randomised trials and other specially constructed studies usually attract significant financial resources and interested investigators. It may be more reasonable to derive standards from studies of operational mammographic screening services whose data, when sufficient studies have been reported, could be assessed to determine performance standards which could reasonably be expected. However, until operational mammography screening services have been shown to produce reduced breast cancer mortality in the screened populations, the results of successful trials must set the gold standard. Acknowledgements The Central & Eastern Sydney Service of BreastScreen NSW and BreastScreen Australia is jointly funded by the Commonwealth and the NSW State Governments. The NSW Central Cancer Registry, which is administered by the NSW Cancer Council and funded by the NSW Health Department, provided valuable assistance with data linkage. References Duffy SW, Tabar L, Fagerberg G, et al. Breast screening, prognostic factors and survival -- results from the Swedish two county study. Br J Cancer 1991; 64: 1133-1138. Day NE, Williams DRR, Khaw KT. Breast cancer screening programmes: the development of a monitoring and evaluation system. Br J Cancer 1989; 59: 954-958. Tabar L, Fagerberg G, Day NE, Holmberg L. What is the optimum interval between mammographic screening examinations? An analysis based on the latest results of the Swedish two-county breast cancer screening trial. Br J Cancer 1987; 55: 547-551. Australian Health Ministers' Advisory Council. Breast Cancer Screening Evaluation Committee. Breast cancer screening in Australia: future directions. Australian Institute of Health, Prevention Program Evaluation Series No. 1. Canberra: AGPS, 1990. National Program for the Early Detection of Breast Cancer -- national accreditation requirements: March 1994. Canberra: Commonwealth Department of Human Services and Health, December 1994. Rickard MT, Lee W, Read JW, et al. Breast cancer diagnosis by screening mammography: early results of the Central Sydney Area Health Service Breast X-Ray Program. Med J Aust 1991; 154: 126-131. Fellegi IP, Sunter AB. A theory for record linkage. J Am Statistical Assoc 1969; 64: 1183-1210. Jaro M. Advances in record linkage methodology as applied to matching the 1985 census of Tampa, Florida. J Am Statistical Assoc 1989; 84: 414-420. Jaro M. Automatch. Generalised record linkage system. Silver Spring, Md: Matchware Technologies Inc, USA, 1994. Taylor R, Smith D, Hfyer A, et al. Breast cancer in New South Wales 1972-91. Sydney: NSW Central Cancer Registry and Cancer Epidemiology Research Centre, NSW Cancer Council, September 1994. Coates M, Day P, McCredie M, Taylor R. Cancer in NSW, incidence and mortality 1992. Sydney: NSW Central Cancer Registry and Cancer Epidemiology Research Centre, NSW Cancer Council, 1995. Armitage P, Berry G. Statistical methods in medical research. 3rd ed. Oxford: Scientific Publications, 1994. Lentner C, editor. Geigy scientific tables. Volume 2: Poisson distribution. Basle, Switzerland: Ciba-Geigy, 1982: 152. Peeters PHM, Verbeek ALM, Hendriks JHCL, et al. The occurrence of interval cancers in the Nijmegen screening programme. Br J Cancer 1989; 59: 929-932. Woodman CBJ, Threlfall AG, Boggis CRM, Prior P. Is the three year breast screening interval too long? Occurrence of interval cancers in NHS breast screening programme's north western region. BMJ 1995; 310: 224-226. Rickard MT, Donnellan M. Diagnosis of small sized invasive breast cancer by an Australian mammography screening service: surrogate end points for mortality reduction. Aust N Z J Surg 1998; 68: 426-429. Robinson JI, Crane CEB, King JM, et al. The South Australian Breast X-Ray Service: results from a statewide mammographic screening programme. Br J Cancer 1996; 73: 837-842. Smith D, Oudod V, Supramaniam R, et al. BreastScreen NSW. Statistical Report 1991-1995. Sydney: NSW Cancer Council, 1996. Coates M, McCredie M, Armstrong B. Cancer in NSW, incidence and mortality 1993. Sydney: Cancer Control Information Centre, NSW Cancer Council, 1996. Parkin DM, Muir CS, Whelan SL, et al, eds. Cancer incidence in five continents. Volume VI. World Health Organization (WHO), International Association of Cancer Registries (IACR), International Agency for Research on Cancer (IARC). Lyon: IARC, 1992. (IARC Scientific Publication No. 120.) Field S, Michell M J, Wallis MGW, Wilson ARM. What should be done about interval breast cancers? BMJ 1995; 310: 203-204. (Received 7 Aug 1997, accepted 3 Apr 1998) Authors' details BreastScreen NSW, Central & Eastern Sydney, Sydney, NSW. Mary T Rickard, FRACR, MPH, Director and Radiologist; Mohamed A Fazli, BScEng, ME, Database Manager; Nadima El Hassan, BEc(Hons), Computer Consultant. Department of Public Health and Community Medicine, Faculty of Medicine, University of Sydney, Sydney, NSW. Richard J Taylor, FAFPHM, FRCP, Associate Professor in Public Health. Reprints will not be available from the authors. Correspondence: Dr M T Rickard, BreastScreen NSW, Central & Eastern Sydney, PO Box 1535, Strawberry Hills, NSW 2012. E-mail: MaryATces.bci.org.au - Readers may print a single copy for personal use. No further reproduction or distribution of the articles should proceed without the permission of the publisher. For permission, contact the Australasian Medical Publishing Company Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au>". <URL: http://www.mja.com.au/>

Mary T Rickard · Richard J Taylor · Mohamed A Fazli

Healthcare

General medicine 17 August 1998 Free

Acupuncture in Australian general practice: practitioner characteristics

Acupuncture in Australian general practice: practitioner characteristics Gary Easthope, Justin J Beilby, Gerard F Gill and Bruce K Tranter MJA 1998; 169: 197-200 For editorial comment, see Komesaroff See also Acupuncture in Australian general practice: patient characteristics Abstract - Introduction - Methods - Results - Discussion - Acknowledgements - References - Authors' details - - ©MJA1998 Abstract Objectives: To ascertain the extent of the use of acupuncture and the characteristics of general practitioners using acupuncture. Design: Secondary analysis of 1996 Health Insurance Commission data on claims by all non-specialist medical practitioners for Medicare Benefits Schedule items for an attendance where acupuncture was performed by a medical practitioner. Main outcome measures: Use of acupuncture by general practitioners and the practitioners' sex, age, place of primary medical qualification, and the socioeconomic disadvantage index of the practitioners' practice. Results: 15.1% of general practitioners claimed for acupuncture. Acupuncture was more likely to be provided by male practitioners, by those aged 35-54 years, and by practitioners who have an overseas primary medical qualification. The socioeconomic index of the practice did not significantly affect the number of claims for acupuncture. Conclusion: Acupuncture is used by about one in seven general practitioners. Its use is associated with middle-aged practitioners, who presumably have more clinical experience. This level of use by experienced doctors suggests that a critical review of the appropriate role of acupuncture in general practice should be considered. Introduction There is interest among general practitioners (GPs) in therapies that are not part of traditional medical practice: alternative or complementary therapies.1-4 A recent MJA editorial stated that: "If 50% of Australians are using alternative treatments each year, it is essential that doctors recognise this fact and be prepared to discuss such use with their patients in a non-judgemental manner",4 while American physicians are exhorted "to begin now to integrate some aspects of alternative medicine into family practice".5General practitioners are heeding this exhortation; alternative treatments are used by 16% of GPs in Britain6,7 and Canada,8 and by 30% in New Zealand.9,10 In Germany, which has a tradition of incorporating alternative therapies into orthodox medicine, 95% of GPs use them.11 Even doctors who do not use such therapies refer patients to medical and non-medical practitioners, at rates ranging from 41% of doctors in Israel12 to 80% in New Zealand.9,10 Non-medical practitioners report that about 10% of their patients are referred from doctors.13 Acupuncture is frequently reported in studies of GPs' use of alternative therapies overseas.6,9,10-12 Meta-analyses on acupuncture,14 homoeopathy15 and spinal manipulation16 do not provide evidence for their efficacy, apart from acupuncture for adult postoperative and chemotherapy nausea and postoperative dental pain,17 and spinal manipulation for lower-back pain.18 Other explanations for adoption of these therapies by doctors must therefore be sought. The fact that medicine is a profession in which clinical judgement is considered paramount is important. Interviews with doctors using alternative therapies in Queensland found they justified such use on the basis of clinical experience.19 We studied use of acupuncture to examine doctors' use of alternative therapies. The primary reason for selecting acupuncture was that information on use was available from Medicare data; a specific item in the Medicare Benefits Schedule (now, item 173; before 1991, item 980) has been used at any attendance where acupuncture was performed by a medical practitioner since 1984. Other alternative therapies do not attract a rebate or are not clearly specified. Acupuncture is of interest in that its cost to Medicare is calculable. Methods The Health Insurance Commission (HIC) provided data on all acupuncture claims by GPs in Australia in 1996. Information was provided on the GPs' sex, age, HIC classification (Box 1) and whether their primary medical qualification was Australian or not. The postcode of each GP's major practice was also identified. To ensure no individual was identifiable, the postcode data were classified into 62 categories (later consolidated to 12 for presentation) derived from an Australian Bureau of Statistics list which allots each postcode an index of socioeconomic disadvantage (SDI).20 The postcode data are used as a surrogate measure of patient characteristics in relation to socioeconomic disadvantage on the assumption that patients generally visit doctors in their home area. Our data include the total population of GPs, and therefore any differences between categories are substantively significant. A logistic regression model was constructed using SPSS.21 Fifty-eight GPs who could not be classified either as vocationally registered or as non-vocationally registered were excluded from the logistic regression analysis. The HIC also provided data on the number of acupuncture claims made each year since 1984, and further data were extracted from the statistics on general practice provided by Medicare.22 The University of Tasmania Human Research Ethics Committee approved the study. Results Since acupuncture became a Medicare benefit item in 1984, claims have risen from 655 000 in the financial year 1984-85 to 960 000 in 1996-97 (Figure). Medicare reimbursements have increased from $7.7 million to $17.7 million. In 1996, 2997 (15.1%) of the 19 783 GPs in Australia claimed at least once for acupuncture, and 62 (0.3%) had acupuncture as their major claimed therapy (Box 2). However, acupuncture claims constituted only 0.7% of all claims by vocationally registered GPs22 and pertained only to 1.2% of patients. Doctors who provided acupuncture had a higher number of non-acupuncture claims than non-providing doctors (population mean, 5029; acupuncture providers' mean, 6632; non-providers' mean, 4743). Non-vocationally registered GPs were less likely than vocationally registered GPs to claim for acupuncture (odds ratio [OR], 0.5), while acupuncture providers were more likely to be men (OR, 1.7), aged 35-54 years (OR, 1.7) and hold primary medical qualifications from outside Australia (OR, 1.6) (Box 3). There was no significant linear or quadratic association between the odds of providing acupuncture and the SDI of the doctor's major practice. The sex and age differentials persisted, with marginally different odds ratios, when GPs were distinguished by whether they provided acupuncture infrequently (less than 1% of services), frequently (1%-25% of services) or extensively (25%-100% of services). However, for frequent and extensive providers, there was no significant difference in the odds of providing acupuncture between those qualified in Australia and those in another country. Discussion There were 960 000 Medicare claims for acupuncture in the 1996-97 financial year, costing $17.7 million in reimbursements. As the HIC data do not include acupuncture services funded by agencies such as Workers' Compensation and the Department of Veterans' Affairs or services provided in public hospitals, these figures understate the total use of acupuncture in Australia. In 1996, 15.1% of GPs in Australia claimed for acupuncture. The proportion of GPs using acupuncture in Australia is comparable to the proportion of German (15%)11 and New Zealand doctors (18%)9,10 who provide this service, but much higher than in the United Kingdom (3%).6 Acupuncture may be more accessible to patients in Australia than these results suggest because about 70% of GPs work in group practices.22 A survey of general practices in Hobart found that, although only 15% (27) of the GPs provided acupuncture, it was available in 31% (20) of practices.23 Interestingly, British research found that the use of alternative therapies was more likely in single or one-partner practices than in group practices.7 This difference between the United Kingdom and Australia may be a function either of the 10-year gap between surveys or of different payment systems. In the United Kingdom doctors are paid a set capitation fee; in Australia a fee-for-service model operates. Choice of therapy is independent of patient demand in the United Kingdom, whereas in Australia patients can "shop around". In Australia, offering a choice of conventional and alternative treatments in group practices may simply be good marketing, so that patients can select one or the other but the practice will not lose income. Doctors who provided acupuncture had a greater provision of all other medical services. This suggests that acupuncture is associated with a propensity to provide more services and a greater variety of services. Whether this means acupuncture is associated with practices that have a more complex mix of patients or presenting complaints can only be resolved by a detailed study. Men were more likely than women to provide acupuncture, and this was not a function of age (the difference remained at each age category except the eldest). In this, as in other respects, women appear to practise medicine differently from men.24 The greater likelihood of doctors aged 35-54 years providing acupuncture may be a function of experience. These practitioners may have had many patients with complaints that have not responded to conventional treatment. Given this experience, they are able to try other therapies and trust their clinical judgement as to efficacy. Those older than 65 years may have been less willing to try alternative therapies, or may have decided such therapies are not effective. There are a number of possible reasons why GPs qualified outside Australia may be more likely to provide acupuncture. These doctors may have studied acupuncture as part of their initial medical training, they may have practices in immigrant areas with high patient demand for acupuncture, or they may be subject to less peer pressure to conform to orthodox practice. Without a more detailed study no one explanation can be confirmed or disproved. Previous reports on consumers of alternative therapies suggest these therapies are the choice of young (aged 25-35 years), well-educated and financially secure people, particularly women.25 If acupuncture is an index of the use of alternative therapies, it should be provided in areas of least disadvantage (SDI categories 11 and 12). This is not the case: there was no clear difference between SDI categories (the least-disadvantaged areas, 11 and 12, having only seven frequent or extensive providers). One explanation may be that acupuncture is not claimed through Medicare in these areas. A survey of acupuncture-providing practices in Hobart suggests this is likely, as most providers (60%; 26) and practices (85%; 20) were in relatively affluent suburbs.23 Residents of such areas may also be receiving acupuncture from non-medical practitioners. Additionally, acupuncture may not be a reliable index of use of alternative therapies because it is available on Medicare. Low-income patients may try acupuncture in preference to orthodox treatments, such as physiotherapy, that they would have to pay for. Acupuncture services in Australia have risen steadily since 1984, and 2997 GPs are using acupuncture throughout Australia. Given this level of use, a study of the appropriate role of acupuncture in Australian primary care medical practice should be considered. Acknowledgements The researchers wish to thank the Government Employees Medical Research Fund, which provided funds to conduct the research. References Wardwell WI. Alternative medicine in the United States. Soc Sci Med 1994; 38: 1061-1068. Paterson C. Complementary medicine [letter]. Br J Gen Pract 1996; 46: 440. Murray RH, Rubel AJ. Physicians and healers -- unwitting partners in health care. N Engl J Med 1992; 326: 61-64. Shenfield GM, Atkin PA, Kristoffersen SS. Alternative medicine: an expanding health industry [editorial]. Med J Aust 1997; 166: 516-517. Gordon JS. Alternative medicine and the family physician. Am Fam Physician 1996; 54: 2205-2212. Wharton R, Lewith G. Complementary medicine and the general practitioner. BMJ 1986; 292: 1498-1500. Anderson E, Anderson P. General practitioners and alternative medicine. J R Coll Gen Pract 1987; 37: 52-55. Verhoef MJ, Sutherland LR. Alternative medicine and general practitioners. Opinions and behaviour. Can Fam Physician 1995; 41: 1005-1011. Hadley CM. Complementary medicine and the general practitioner: a survey of general practitioners in the Wellington area. N Z Med J 1988; 101: 766-768. Marshall RJ, Gee R, Israel M, et al. The use of alternative therapies by Auckland general practitioners. N Z Med J 1990; 103: 213-215. Himmel W, Schulte M, Kochen MM. Complementary medicine: are patients' expectations being met by their general practitioners? Br J Gen Pract 1993; 43: 232-235. Borkan J, Neher JO, Anson O, Smoker B. Referrals for alternative therapies. J Fam Pract 1994; 39: 545-550. Fulder SJ, Munro RE. Complementary medicine in the United Kingdom: patients, practitioners, and consultations. Lancet 1985; 2: 542-545. ter Riet G, Kleijnen J, Knipschild P. Acupuncture and chronic pain: a criteria-based meta-analysis. J Clin Epidemiol 1990; 43: 1191-1199. Kleijnen J, Knipschild P, ter Riet G. Clinical trials of homoeopathy. BMJ 1991; 302: 316-323. Shekelle PG, Adams AH, Chassin MR, et al. Spinal manipulation for low-back pain. Ann Intern Med 1992; 117: 590-598. Acupuncture. NIH Consensus statement online 1997 November 3-5 [4 February 1998]; 15. In press. Ernst E. Complementary medicine -- doing more good than harm? Br J Gen Pract 1996; 46: 60-61. Eastwood H. General medical practice, alternative medicine and the globalisation of health [doctoral thesis]. Brisbane: University of Queensland, 1997. Castles I, Information paper: 1991 census. Socio-economic indexes for areas. Canberra: AGPS, 1994. (Catalogue no. 2912.0.) SPSSx statistical package for the social sciences [computer program]. Chicago, Ill: SPSS Inc, 1997. Commonwealth Department of Health and Family Services. General practice in Australia: supplementary tables 1997. Canberra: AGPS, 1997. Bombardieri D. Convergence between orthodox and alternative therapies in Hobart, Tasmania [Honours thesis]. Hobart: University of Tasmania, 1997. Britt H, Bhasale A, Miles DA, et al. The sex of the general practitioner: a comparison of characteristics, patients, and medical conditions managed. Med Care 1996; 34: 403-415. MacLennan AH, Wilson DH, Taylor AW. Prevalence and cost of alternative medicine in Australia. Lancet 1996; 347: 569-573. (Received 7 Jan, accepted 17 Apr 1998) Authors' details Department of Sociology and Social Work, University of Tasmania, Hobart, TAS. Gary Easthope, MA, PhD, Associate Professor; Bruce K Tranter, BA, PhD, Lecturer. Department of General Practice, University of Adelaide, SA. Justin J Beilby, MPH, FRACGP, Senior Lecturer. Division of Community and Rural Health, University of Tasmania, Launceston, TAS. Gerard F Gill, MAE, FRACGP, Clinical Senior Lecturer. Reprints will not be available from the authors. Correspondence: Dr G Easthope, Department of Sociology and Social Work, University of Tasmania, GPO Box 252C-17, Hobart, TAS 7001. E-mail: Gary. EasthopeATutas.edu.au - Readers may print a single copy for personal use. No further reproduction or distribution of the articles should proceed without the permission of the publisher. For permission, contact the Australasian Medical Publishing Company Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au>". <URL: http://www.mja.com.au/>

Gary Easthope · Justin J Beilby · Gerard F Gill · Bruce K Tranter

For debate

Cardiovascular diseases 11 February 1999 Free

The 100-year conflict: salt intake and cardiovascular disease

For Debate The 100-year conflict: salt intake and cardiovascular disease MJA 1998; 169: 174-180 The health effects of dietary salt have long been debated. As early as the beginning of the 20th century, salt restriction was used as a therapeutic measure, first for oedema and then for hypertension, particularly in France.1 Later, in the United States, the benefits of low salt diets for patients with hypertension and renal disease were championed by Allen in the 1920s and 30s and by Kempner in the late 1930s and 40s.1 However, not all investigators were convinced of the value of these diets, and the hazards of overzealous and prolonged salt restriction were also appreciated.1 By the 1960s and 70s, studies linking an increase in blood pressure of indigenous populations with the introduction of salty Western diets persuaded government bodies to recommend reduced salt as part of healthy dietary guidelines. One of the eight Dietary Goals for Australia, announced in 1979 by the then Commonwealth Department of Health, was "Decrease consumption of salt".2 There are, however, many researchers who maintain that there is insufficient evidence of benefit to recommend universal salt restriction. A summary of this controversy, described as "a philosophical clash between the requirements of public health policy and the requirements of good science", appeared in Science last year.3 In the MJA the salt controversy is alive and well. A study by Beard et al published in 1997 showing a low level of conformity with the year 2000 dietary salt target for Australians (<100mmol/day)4 brought an immediate response from Kincaid-Smith, reminding readers of the possible dangers of low salt intake.5 Then, in March 1998, a study by Alderman et al in the Lancet, claiming to have found an inverse association between dietary salt intake and all-cause and cardiovascular disease mortality,6 revived the international controversy, to which the Lancet's letters columns attest.7-10 Here, we present our own salt debate, with three views of the value (or otherwise) of salt restriction as part of a healthy diet. Universal recommendations for sodium intake should be avoided Restriction of salt intake is needed too ameliorate the cardiovascular disease epidemic The salt dilemma: some answers, many questions Link to salt debate references Dr Derek Denton showed unequivocally that increased salt intake causes a substantial rise in blood pressure in chimpanzees.11 Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au>". <URL: http://www.mja.com.au/>

Next Issue Volume 169 Issue 5

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Editorials 7 September 1998 Free

Peer review on the Internet: launching eMJA peer review study 2

Craig Bingham

Editorials 7 September 1998 Free

Paediatric rotavirus gastroenteritis: where to now in prevention and treatment?

Mark J Ferson · Richard Henry

Research 7 September 1998 Free

Re-engineering the elective surgical service of a tertiary hospital: a historical controlled trial

Gideon A Caplan · Ann Brown · Philip J Crowe · Su-Jen Yap · Shaune Noble

Research 7 September 1998 Free

Rotavirus infection and rates of hospitalisation for acute gastroenteritis in young children in Australia, 1993-1996

John B Carlin · Patty Chondros · Paul Masendycz · Helen Bugg · Ruth F Bishop · Graeme L Barnes

Previous Issue Volume 169 Issue 3

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Editorials 3 August 1998 Free

Matters of life and death: the challenge of CPR decision making

Christopher J Ryan

Editorials 3 August 1998 Free

Twenty-four hour access to health information and advice

Frank Oberklaid

Editorials 3 August 1998 Free

General practice stress

Robert M Douglas · Beverly M Sibthorpe

Research 3 August 1998 Free

Decision making in CPR: attitudes of hospital patients and healthcare professionals

Ian H Kerridge · Sallie-Anne Pearson · Isobel E Rolfe · Michael Lowe

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