Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
BMJ 2006;332:538-541 (4 March), doi:10.1136/bmj.332.7540.538
Karsten Juhl Jørgensen, research fellow1, Peter C Gøtzsche, director1
1 Nordic Cochrane Centre, Rigshospitalet Department 7112, Blegdamsvej 9, DK-2100 Copenhagen, Denmark
Correspondence to: K J Jørgensen kj{at}cochrane.dk
The benefits and harms of screening for breast cancer are delicately balanced and women should decide for themselves, on an informed basis. Do the invitations give enough information to enable this?
Invitations to screening mammography play a central part in the process of obtaining informed consent. It is the only source of information distributed to all potential participants. Other sources, such as pamphlets and websites, have been shown to be information poor and biased in favour of participation,1 2 w1 w2 and information from the media and doctors is likely to vary and be unevenly distributed. We examined mammography invitations from English speaking and Scandinavian countries with publicly funded screening to assess whether they provide sufficient information to enable women to make an informed decision.
When a society decides to offer cancer screening, eligible citizens need to be made aware of the programme. A letter of invitation is a common approach, and it seems obvious to use this letter to provide balanced information about benefits and harms of screening, particularly since there is international consensus that participation in cancer screening should be based on informed consent.3 w3 w4 However, in countries with publicly funded screening, those responsible for the success of the programme are also those who provide the information. Herein lies a potential conflict of interest. High participation rates are pivotal to any screening programme, but information about potential harms may deter women from participation.
|
Women generally exaggerate the benefits and are unaware of the harms of screening.4-6 The authors of a study of American and European women4 raised doubts about informed consent procedures since 68% believed screening reduced their risk of contracting breast cancer, 62% that screening at least halved mortality, and 75% that 10 years of screening saved 10 of 1000 participants, which is 10 times the most optimistic estimates.7-9 Other studies have shown that only 8% of women were aware that participation has the potential to harm healthy women,5 that 15% believe their lifetime risk of contracting the disease is more than 50% (an overestimate of about 5 times),6 and that one third think screening detects more than 95% of breast cancers.w5
We collected invitations to mammography screening from Australia, Canada, Denmark, New Zealand, Norway, Sweden, and the United Kingdom. These countries all have publicly funded screening programmes that are nationally or regionally coordinated and use languages we can read. We requested letters that invited women for the first time including any enclosed pamphlets, letters to non-responders, and invitations to subsequent screening rounds. We focused on the initial invitation, which is most commonly sent out as women turn 50 years of age. We contacted organising units by email, telephone, or post and made three requests in case of non-response. Material was collected between October 2004 and February 2005.
We recorded whether a date of appointment was issued in the invitation, whether a reminder letter or other means of contact was used for non-responders, whether suggestive headlines or appeals for participation were used, and whether regular breast self examinations, clinical breast examinations, or both were recommended, as an additional check on whether the information was evidence based.10 We evaluated the invitations independently and settled any discrepancies by discussion. We used the same checklist of 17 information items on benefits and harms as in our previous study of websites,2 most of which have been used in other studies of information materials.1 w1
We identified 51 coordinating units and 33 (65%) responded. The unit in southern Australia declined to supply a sample as it was revising its invitation, and Nova Scotia, Canada, did not issue invitations but used public advertising. Thus, we obtained samples from 31 areas, including all seven countries. For Norway and the UK, we evaluated a national sample letter. In the UK, this letter may be modified locally, but the accompanying pamphlet, which contains the bulk of the information, is the same. The Norwegian letter and pamphlet are used nationwide. The response rate was lower for Sweden than for other countries (9/22 regions), but this is unlikely to have influenced our overall findings because the information varied little among those that responded.
Since the wording and contents differed little within each country, our main emphasis is on the national results (see table on bmj.com). Twenty one invitations (68%), at least one from each country, gave an appointment date, but in New Zealand women receive a letter only after registering with the programme. Reminder letters were used in 18 of 31 areas (58%) but not in Sweden or the UK. In New Zealand, women who do not attend their appointment are telephoned, and in Western Australia and some areas of New Zealand, a letter is sent to general practitioners informing them about non-responders and asking them to discuss this with the woman at the next consultation. These national differences limit the applicability of our results to countries we did not include, in particular countries where screening is a private enterprise.
The invitations included a median of 2 of the 17 possible information items in our survey, ranging from none in Sweden to six in New Zealand. A pamphlet was included with 20 invitations (65%), but only in one of nine invitations in Sweden.
Thirty invitations (97%) mentioned the main benefit of screening, a reduction in breast cancer mortality, but only seven (three countries) gave the size of the benefit and they all described it as a relative risk reduction rather than an absolute risk reduction or the number needed to screen. The effect of screening on total mortality was not mentioned. In contrast, no invitation mentioned the major harm of screening, overdiagnosis and subsequent overtreatment.
Six invitations (five countries) argued that screening leads to less invasive surgery and four additional invitations (one additional country) that it leads to simpler treatment. None of the invitations noted the uncertainties related to treatment of carcinoma in situ or the increased use of surgery and radiotherapy arising from overdiagnosis.
The most commonly mentioned harm was pain associated with the procedure (15 invitations (48%), six countries), but it was downplayed in eightfor example, "Any discomfort should only last a few seconds" (Breast-Screen Western Australia). The lifetime risk of developing breast cancer was noted in 10 invitations (32%, six countries) and estimates varied from 1 in 9 to 1 in 13.
Recall rates for further examinations appeared in six invitations (19%), but as the risk in each screening round, not the accumulated risk. After 10 screens, the accumulated risk of recall is about 50% for American women11 and about half as much for European women.12 About a quarter of these women will have a biopsy or fine needle aspiration.9 A false positive result can have a profound psychological effect on women and their families because it raises the suspicion of a potentially life threatening disease.13
Seven invitations mentioned screening sensitivity, but five were misleading. For example, the Manitoba pamphlet states that "about 1 out of every 10 breast cancers cannot be seen on a mammogram," a 90% detection rate. This obscures the fact that many, indeed the most dangerous, cancers are detected in the intervals between screening rounds.3 Interval cancer rates of up to 50% are deemed acceptable with biennial screening according to European guidelines.w4 Neither specificity nor positive predictive value was mentioned.
Fifteen invitations (48%) recommended regular breast self examination, clinical breast examinations, or both. This is despite evidence that self examination leads to a doubling in biopsy of benign growths and probably has no mortality benefit10 and the lack of evidence for an effect of clinical breast examinations.3 9
Appeals for participation appeared in only one of nine letters in Sweden, but in 17 of the remaining 22for example, "We strongly recommend that you use this free service" (Northern Territory, Australia). Seven reminder letters had stronger pleas than the first letter (box 1).
Nineteen pamphlets (95%) had suggestive headlines, such as, "Have a screening mammogram, it may save your life" (Western Australia) and "Why is having a breast screen a good idea?" (New South Wales, Australia).
Although it is good news that the invitations often included an information pamphlet, the focus on the benefits of screening is problematic. The benefits were framed positively, avoiding absolute risk reductions and number needed to treat, which are easier to understand and provide more realistic expectations.14 The reduction in breast cancer mortality was given as 25-30%, although recent systematic reviews have either doubted the effect8 or suggested relative risk reductions of 15%-21%.9 15 These estimates do not convey that they apply only to the period when women are screened and are not a reduction in lifetime risk.
|
The most important harms, overdiagnosis and overtreatment, were not mentioned and other important harms were often either omitted or downplayed. The estimated level of overdiagnosis, 30% in the randomised trials,8 is supported by large epidemiological studies that have suggested 40-60%.16-20 Carcinoma in situ is a special case as it is rarely detected without screening and represents about 20% of all screen detected cancers.3 Little is known about its natural course, but autopsy studies indicate that many lesions do not progress.21 Because it is impossible to tell which lesions will become invasive, all are treated, often with mastectomy and radiotherapy.8 9
Overdiagnosis led to screening programmes for neuroblastoma in children being stoppedw6 and is a main reason why screening for prostate and lung cancer is generally discouraged.22 Very few women are aware that screening can detect non-progressive cancer,23 and probably even fewer know that invasive cancer can sometimes regress spontaneously.w7 Many will falsely believe their lives have been saved by screening, when in fact they have only been physically and psychologically harmed.
Participation rates increase when there is a pre-assigned date of appointment,3 24 but we find this approach problematic as it bypasses the informed consent step and gives the impression that participation is a public duty. Information material should convey the message that a decision not to attend mammography screening can be based on sound reasoning and is not irresponsible, as is currently believed by about 75% of 55 year old Americans.5
Fear of cancer seems to increase participation in breast cancer screening,w8 and the frequent mention of lifetime risk of developing breast cancer in the information could scare some women to participate without considering the harms, especially as these were so rarely mentioned.
More comprehensive information will lead to more women declining to be screened.w9 Uptake rates in Sweden are high, 78-84%,3 which may be related to the fact that the invitations contain little information apart from a date of appointment and explanations of practical matters such as transport and payment of a small fee.
Informed consent cannot be achieved solely through information in invitations. It is a process that should include a discussion with a general practitioner, as preferred by 88% of Swiss women.w10 It is not reasonable to assume that participants have been adequately informed about important harms through other sources. We believe that the information included with invitations should be more balanced, using absolute numbers to describe the likelihood of benefits and harms,19 and applying to the same time span if possible (box 2). Furthermore, we suggest that the responsibility for the programmes should be separated from the responsibility for the information material and that consumer groups be involved in the process of developing balanced information material.
|
|
References w1-w11 and details of invitations are on bmj.com
We thank those who supplied material, Hazel Thornton for contact details for the UK screening programme, and Kay Dickersin for comments on our manuscript.
Contributors and sources: We have previously evaluated information on mammography screening on websites and PCG was involved in a systematic review of the breast screening trials, which questioned the value of screening. Both authors contributed to conceiving the project. The draft protocol was written by KJJ and revised by PCG. KJJ collected the invitations and wrote the first manuscript. Both authors extracted data and contributed to the interpretation and final manuscript. Both are guarantors.
Competing interests: None declared.
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
Read all Rapid Responses
What can you learn from this BMJ paper? Read Leanne Tite's Paper+