- Research article
- Open Access
Exploring general practitioners' experience of informing women about prenatal screening tests for foetal abnormalities: A qualitative focus group study
BMC Health Services Research volume 8, Article number: 114 (2008)
Recent developments have made screening tests for foetal abnormalities available earlier in pregnancy and women have a range of testing options accessible to them. It is now recommended that all women, regardless of their age, are provided with information on prenatal screening tests. General Practitioners (GPs) are often the first health professionals a woman consults in pregnancy. As such, GPs are well positioned to inform women of the increasing range of prenatal screening tests available. The aim of this study was to explore GPs experience of informing women of prenatal genetic screening tests for foetal abnormality.
A qualitative study consisting of four focus groups was conducted in metropolitan and rural Victoria, Australia. A discussion guide was used and the audio-taped transcripts were independently coded by two researchers using thematic analysis. Multiple coders and analysts and informant feedback were employed to reduce the potential for researcher bias and increase the validity of the findings.
Six themes were identified and classified as 'intrinsic' if they occurred within the context of the consultation or 'extrinsic' if they consisted of elements that impacted on the GP beyond the scope of the consultation. The three intrinsic themes were the way GPs explained the limitations of screening, the extent to which GPs provided information selectively and the time pressures at play. The three extrinsic factors were GPs' attitudes and values towards screening, the conflict they experienced in offering screening information and the sense of powerlessness within the screening test process and the health care system generally. Extrinsic themes reveal GPs' attitudes and values to screening and to disability, as well as raising questions about the fundamental premise of testing.
The increasing availability and utilisation of screening tests, in particular first trimester tests, has expanded GPs' role in facilitating women's informed decision-making. Recognition of the importance of providing this complex information warrants longer consultations to respond to the time pressures that GPs experience. Understanding the intrinsic and extrinsic factors that impact on GPs may serve to shape educational resources to be more appropriate, relevant and supportive.
Recent developments have made screening tests for foetal abnormalities available earlier in pregnancy and women have a range of testing options accessible to them. It is now recommended that all women, regardless of their age, are provided with information on prenatal screening tests [1, 2]. The provision of information is an essential component in facilitating women's informed decision-making [3–6]. At a minimum, women need to understand the condition(s) for which the testing is being offered, the characteristics of the test and the implications of testing .
Health professionals need to provide women with information on both the benefits and inherent limitations of screening tests in a way that optimises understanding, without increasing their level of anxiety [7–9]. This is particularly true of tests screening for foetal abnormality where decisions on diagnostic testing and/or termination of an affected pregnancy may arise.
The quality of information women have received has been found to be variable , while women have consistently demonstrated low levels of knowledge about prenatal screening for foetal abnormalities [3, 5, 6, 10–13]. Consequently, there are challenges for all pregnancy care providers as well as implications for practice.
The introduction of screening tests in the first trimester of pregnancy has resulted in extending the role of General Practitioners (GPs). When providing confirmation of pregnancy, GPs are often the first health professional the woman consults. If this is in the first trimester, women are more likely to have all the prenatal test options available and have time to consider the information provided. As a primary health care provider the GP is well positioned to inform women of the increasing range of screening tests available.
Women value quality information that is provided by the health professional in a timely manner . This requires the health professional to have a sound understanding of the relevant issues and be able to communicate this information. While studies have focused on exploring the knowledge and attitudes of health professionals towards prenatal testing [15–18], the effect on health professionals of providing this information to women has not received much attention. The purpose of this study was to explore GPs' experience of informing women about prenatal genetic screening tests for foetal abnormality.
The study was conducted to inform the development of a decision aid for prenatal testing for foetal abnormalities, as part of a randomised controlled trial called the ADEPT (A DEcision aid for Prenatal Testing) study [ISRCTN22532458] [19, 20].
Focus groups interviews were used in preference to individual interviews as the synergistic effects of a group setting may result in the production of ideas that might not have been uncovered in individual interviews . Purposive sampling  was employed to ensure both male and female GPs from rural and metropolitan practices participated, thereby increasing the heterogeneity of experiences and perspectives. Contact details were obtained from the on-line public telephone listings and GPs from targeted geographical areas were invited to participate in the study. GPs were also recruited from a variety of professional medical organisations. The team of investigators was comprised of a midwife (CN), an associate genetic counsellor (SL), a psychologist (BM), a general practitioner (JG) and two epidemiologists (JH and RB).
Informational redundancy was reached following four focus groups and no further groups were conducted in accordance with standard qualitative methodology . The same facilitator (SL) and co-facilitator (CN) conducted all focus groups, using a semi-structured discussion guide to explore GPs' experiences. A literature review and the expertise of the project team informed the content of the question topics. The development of the discussion guide (Appendix) was informed by the method outlined by Greenwood and Parsons . Audio-tapes of the sessions were professionally transcribed and the accuracy of the transcripts was verified using the raw data and field notes.
The analysis involved a constant comparison approach , with SL and CN repeatedly reading the transcripts to develop an agreed set of codes. The analysis was also guided by the conceptual qualitative research framework of Miles and Huberman . One of the strengths of this framework lies in the explicitness of its description of qualitative data analysis, which includes the use of highly structured data displays to tease out relationships, synthesise findings and help guide against potential researcher bias. Data analyses were iterative and SL, RB & CN participated in this process to identify and agree upon emergent themes and discuss their face validity. The analysis took place concurrently with data collection, and results from each focus group were used to suggest additional lines of questioning in subsequent focus groups to ensure that divergent points of view would be expressed. The use of multiple coders and analysts and informant feedback are strategies recommended by Miles and Huberman to reduce the potential for researcher bias and increase the validity of the findings . A draft manuscript was reviewed by four GPs who participated in different groups to authenticate the findings as representative of discussions and modify accordingly. In addition, a modified version of the clustered matrices described by Miles and Huberman  was used to facilitate analysis within and across groups. A code was used to de-identify responses comprising of a sequence of two digit codes for the group and the participant. Ethics approval was obtained from the Royal College of General Practitioners, Australia (ref NREEC 03-16) to conduct the study. All participants provided written consent to participate in the study.
Two groups were held in metropolitan locations and two in regional settings in Victoria, one of the south-eastern states of Australia, where approximately 63,000 women give birth each year . In Australia the GP's role can vary from, at a minimum, confirming pregnancy and providing referral, to sharing pregnancy care with another provider (midwife, obstetrician) through to providing care in labour and the postnatal period. Prenatal care arrangements vary in different Australian States; in Victoria, women booked to give birth at publicly funded maternity services have access to a second trimester maternal serum screening test free of charge. Women in the public system who are at increased risk of foetal abnormality on the basis of their screening test result or their age (37 years or older by expected due date), are offered a funded diagnostic test at a tertiary hospital. Other screening tests, including nuchal translucency, combined first trimester screening and second trimester foetal anomaly ultrasounds, as well as diagnostic tests are available to all women on a fee for service basis.
In total twenty-seven GPs expressed interest and all participated: 18 female and 9 male. Six themes important in understanding GPs' experiences of informing women about screening tests were identified as common across the four groups. The themes were conceptualised as either intrinsic or extrinsic factors. Intrinsic factors describe the elements within the context of the consultation that impact on GPs. Extrinsic factors describe elements that operate beyond the scope of the consultation and have a broader impact on GPs. To further illustrate these six themes, the roles GPs adopt in response to both intrinsic and extrinsic factors are detailed in Table 1.
Three factors occurring within the context of the consultation were consistently evident across all groups when the topic of screening was first broached by the GP. First, the limitations of screening was a central intrinsic factor. Another was the extent to which GPs filtered the complex information, and how they facilitated decision-making based on their own perceptions of the woman's information needs. The third related to time constraints, which was a pervasive factor across all aspects of communicating screening test information.
Limitations of screening
In order to inform women of screening tests, GPs related difficulties in communicating the complex information about the limitations of screening to women. Quotes to illustrate these views are shown in Table 2. All GPs reported presenting numerical expressions of probability in a way that was meaningful, particularly as there was strong agreement that women generally had a poor understanding of statistics.
Communicating the inherent limitations of screening tests to the woman was reported as being a challenging experience for GPs. For many GPs, central to interpreting this complex information for women was the issue of grappling with the notions of risk and uncertainty, which challenged GPs on a number of levels. Not being able to provide a definitive answer was perceived as being a particularly difficult task. For some GPs, screening test discussions exposed their own lack of confidence or skill in dealing with screening test information. Providing a pre-test probability that was meaningful and conveying that a residual risk would exist, without causing anxiety, were also identified as difficulties.
GPs identified themselves as an important source of screening test information for the woman. There was considerable variation in the amount, level and delivery of information on screening tests that GPs provided. From the transcripts it was evident that many GPs provided information to women selectively, based on their perceptions of the woman's information needs, as well as the decision-making style they used within the consultation.
Acting as the 'gatekeeper of information', GPs demonstrated how testing can be presented differently to women, usually on the basis of maternal age or parity (Table 3). This was a deliberate process on the part of some GPs, yet for others it appeared to occur unintentionally. Some GPs who could be classified as providing information selectively to women also appeared to use a directive style within the consultation. GPs who indicated they communicated using a less directive decision-making style and involved the woman in decision-making, appeared less likely to act in a gatekeeper role.
When asked who tended to raise the issue of prenatal testing, seldom was the provision of screening information explained in terms of being at the woman's initiation. When women did raise the issue of testing, it was often explained in terms of women asking for the GP's personal recommendation, "...that's a question I commonly get asked – what would I do?" 0204
GPs described time pressures related to informing women about prenatal testing for foetal abnormalities as a significant source of stress. Time constraints were experienced because of the limitations of screening, the need for the information to be provided early in pregnancy and the competing pregnancy-related information the GP wanted to provide to the woman (quotes shown in Table 4). The first consultation in pregnancy was described as being information-laden and the discussions about testing increased time pressures.
The GP was seen as being required to act as a 'timekeeper' because screening test information was said to take a considerable amount of time to explain. Consistently GPs related that they had insufficient time to cover the topic and that it required an entire consultation, but seldom was this possible.
The introduction of first trimester screening tests has meant that it is often not appropriate for the GP to defer a discussion of these tests. GPs described how this imperative of time had negative consequences for the woman and themselves.
The following three factors have been classified as extrinsic as they consist of elements that impact on the GP, beyond the scope of the consultation. They reveal GPs' attitudes and values to screening and to disability, as well as raising questions about the fundamental premise of testing. Extrinsic factors also include perceptions by GPs of their role within the screening test process and the health care system generally.
In providing information about screening tests to women, GPs voiced the importance of addressing why the tests were being offered and the possible consequences of having a screening test. GPs identified the negative impact on GPs of providing this information earlier in pregnancy than was required previously when women presented, happy with the confirmation of their pregnancy, and the GP needed to introduce the topic of testing (Table 5).
The GP was cast in the role of the 'bearer of bad news' through introducing the topic of testing which included the risk of foetal abnormality, the limitations of screening, the role of diagnostic testing and the option of termination of pregnancy in the event of a major abnormality.
The apparent moral obligation to provide information on screening tests was in conflict with the GPs' perceptions of screening tests as having potentially negative implications for the woman, society and themselves (Table 6). The inherent limitations of a population screening approach further exposed this conflict. In their role as the 'moral agent', providing information on testing and offering the tests was identified by some GPs as having the potential to do more harm than good.
GPs related a concern for women who would be made unduly anxious about the possibility of foetal abnormality. This was particularly true for young women where "a very large number" of young women would be "put through the anxiety" (0303) of testing for a single woman to benefit.
GPs in the role of the 'moral agent' were also concerned with the difficulty of "taking into account someone's own ethical or moral perspective"(0404). Using language that did not bring a personal value system into the consultation was viewed as troublesome.
The provision of information to women on screening tests caused some GPs to question how disability was being valued in society and whether or not they were implicated in promoting the 'perfect child'.
GPs expressed issues of powerlessness relating to how they viewed their role in the screening process (Table 7). In part this was related to a difficulty in accessing and keeping up-to-date with testing information. This was discussed in terms of the demands of their generalist workload, numerous recent developments in screening as well as being up-to-date with practical aspects like cost and the quality of local testing providers.
GPs in the role of the 'intermediary' described themselves as acting as an advocate for the women, trying to empower them to make an informed choice regarding testing and avoid being coerced into testing by obstetricians who may present testing as "routine" or "compulsory".
GPs also described the frustration of poor communication from other health care providers and from problems with the screening system particularly in offering screening tests to women who are "not fully informed."
The findings of our study expose the considerable impact that informing women of prenatal screening tests for foetal abnormality has on GPs. The identification of intrinsic and extrinsic factors present a framework of describing the observed differences between factors that are contained within the consultation and factors that have a more pervasive impact on the GP. The consistency of the findings across different focus groups underscores the salience of the experience of GPs described. We propose that in order to improve women's capacity to make an informed decision about screening, attention needs to be directed to better support the GP's role.
The impact on GPs that we have described is only partially explained by their lack of knowledge. In particular, responsive professional development activities need to be directed to the complexity of factors impacting on the GP experience. Educational activities that embrace intrinsic factors should include epidemiological content and focus on communicating complex issues like 'risk' and 'uncertainty'. A framework such as the patient-centred clinical method  within an interactive learning environment could provide the opportunity for GPs to explore ways to 'find common ground' in decision-making and be less directive in the information they provide.
GPs already work within significant time constraints. Other health professionals have previously reported the intrinsic factor 'time pressures' experienced by GPs in our study when informing women of screening [29, 30]. The number of options for prenatal testing and the availability of earlier tests make extra demands on the GP's already limited time. The lack of time available to discuss prenatal testing is at odds with the increasing importance of the GP's role in informing women of screening. With the utilisation of prenatal screening increasing , it is timely to consider how to increase the amount of time allocated to consultations in early pregnancy. One option applicable to the Australian health care system might be to fund these complex discussions as long consultations, which attract a higher Medicare (Australia's publicly-funded universal health care system) rebate.
Extrinsic factors that impact on the GP beyond the scope of the consultation also warrant consideration. Our findings indicate the importance of GPs' values and attitudes to tests, screening and disability, in explaining how they experience their role in informing women. It is important that educational activities acknowledge and embrace the range of values and attitudes that exist. It may also be beneficial to consider creating forums for peer discussions about challenging experiences.
Even in a group practice, GPs often function in an isolated manner with limited opportunity to discuss issues relating to consultations. For example, during one focus group a GP revealed a professional concern to the group that the GP had not talked about previously to anyone. In light of the difficulties experienced by GPs in this study, a mechanism for GPs to share and reflect on their experiences may prove beneficial. For instance, the experience of genetic counsellors promote the benefit of 'supervision' , supporting the professional and providing a non-threatening environment to discuss psychosocial aspects of consultations.
The purpose of using a qualitative design to address this research question was to document the range of GP experiences to facilitate an in depth analysis of issues in the hope that these finding will make a valuable contribution to achieving a better understanding of GPs' experience of screening. However, only quantitative studies can unpack the degree to which these experiences and beliefs are endorsed.
This study provides a lens through which to view complex primary health consultations. Facilitating women's informed decision-making regarding prenatal screening tests requires much more from the GP than the provision of appropriate information under significant time constraints; moral dimensions also exert an influence.
An understanding of epidemiological language and communication skills is needed by GPs to assist them in providing women with meaningful information. However, it is important that the scope of future educational programs is broader than solely providing GPs with information and education. Consideration of GPs' values and attitudes may well serve to make educational resources more appropriate, relevant and supportive. Educational activities that fail to explore attitudes and values of participants to disability, screening and termination of pregnancy may be considered fundamentally flawed.
Appendix: discussion guide for focus groups
When I say the words "prenatal testing for Down syndrome", what is the first thing that comes into your mind?
Generally, how much do you think GPs know about prenatal testing?
How often does prenatal testing come up as a topic for discussion during your consultations with pregnant women?
Do you raise the issue of prenatal testing with pregnant women or do they tend to bring it up?
How do you go about discussing prenatal testing with pregnant women?
What questions do women commonly ask you about prenatal testing?
How much time do you spend in discussing prenatal testing with women?
Tell me about your recent experiences discussing prenatal testing with your patients.
What do you find most difficult about discussing prenatal testing?
What are the key points about prenatal testing that you think women need to understand in order to make a decision about what is best for them?
What resources do you use to discuss prenatal testing and how helpful are they?
Are there other resources that you use for other health related matters that you commonly use that you find useful?
When do you think would be the best time to discuss prenatal testing and hand out a decision aid?
Are there any other issues that you would like to raise?
Royal Australian and New Zealand College of Obstetricians and Gynaecologists and Human Genetics Society of Australasia Joint Committee, Ellwood D, de Crespigny L, Halliday J, McLennan A, McMillan J, et al: Antenatal screening for Down syndrome and other fetal aneuploidy. Obstetrics and Gynecology. 2000, 2 (3): 185-190. [http://www.health.vic.gov.au/perinatal/downloads/annrep0304.pdf]
Royal College of Obstetricians and Gynaecologists: Antenatal screening for Down syndrome. [http://www.rcog.org.uk/resources/public/pdf/down_syndrome_screening.pdf]
Kohut RJ, Dewey D, Love EJ: Women's knowledge of prenatal ultrasound and informed choice. Journal of Genetic Counseling. 2002, 11 (4): 265-276. 10.1023/A:1016378415514.
Marteau TM, Dormandy E: Facilitating informed choice in prenatal testing: how well are we doing?. American Journal of Medical Genetics. 2001, 106: 185-190. 10.1002/ajmg.10006.
Al-Jader LN, Parry-Langdon N, Smith RJW: Survey of attitudes of pregnant women towards Down syndrome screening. Prenatal Diagnosis. 2000, 23-29. 10.1002/(SICI)1097-0223(200001)20:1<23::AID-PD746>3.0.CO;2-T.
Gekas J, Gondry J, Mazur S, Cesbron P, Thepot F: Informed consent to serum screening for Down syndrome: are women given adequate information?. Prenatal Diagnosis. 1999, 19: 1-7. 10.1002/(SICI)1097-0223(199901)19:1<1::AID-PD456>3.0.CO;2-S.
Santalahti P, Latikka AM, Ryynanen M, Hemminki E: Women's experiences of prenatal serum screening. Birth. 1996, 23 (2): 101-107. 10.1111/j.1523-536X.1996.tb00837.x.
Watson M, Hall S, Langford K, Marteau TM: Psychological impact of the detection of soft markers on routine ultrasound scanning: a pilot study investigating the modifying role of information. Prenatal Diagnosis. 2002, 22: 569-575. 10.1002/pd.373.
Hall S, Bobrow M, Marteau TM: Psychological consequences for parents of false negative results on prenatal screening for Down's syndrome: Retrospective interview study. British Medical Journal. 2000, 320: 407-412. 10.1136/bmj.320.7232.407.
Jaques A, Halliday J, Bell R: Do women know that prenatal testing detects fetuses with Down syndrome?. Journal of Obstetrics and Gynaecology of India. 2004, 24 (6): 647-651. 10.1080/01443610400007885.
De Vigan C, Vodovar V, Goujard J, Garel M, Vayssiere C, Goffinet F: Mothers' knowledge of screening for trisomy 21 in 1999: a survey in Paris maternity units. European Journal of Obstetrics, Gynecology, & Reproductive Biology. 2002, 104 (1): 14-20. 10.1016/S0301-2115(01)00559-0.
Mulvey S, Wallace E: Women's knowledge and attitudes to first and second trimester screening for Down's syndrome. BJOG. 2000, 107 (10): 1302-1305. 10.1111/j.1471-0528.2000.tb11624.x.
Grewal GK, Moss HJ, Aitken DA, Bjornsson S, Cameron AD, Pell JP: Factors affecting women's knowledge of antenatal serum screening. Scottish Medical Journal. 1997, 42 (4): 111-113.
Carroll J, Brown J, Reid A: Women's experience of maternal serum screening. Canadian Family Physician. 2000, 46: 614-620.
Hemminki E, Santalahti P, Toivianen H: Impact of prenatal screening on maternity services - Finnish physicians' opinions. Acta Obstetricia et Gynecologica Scandinavica. 1999, 78 (2): 93-97. 10.1034/j.1600-0412.1999.780204.x.
Ormond K, Gill C, Semik P: Attitudes of health care trainees about genetics and disability: Issues of access, health care communication, and decision making. Journal of Genetic Counseling. 2003, 12 (4): 333-349. 10.1023/A:1023953022290.
Rostant K, Steed L, O'Leary P: Prenatal screening and diagnosis: A survey of health care providers' knowledge and attitudes. Australian and New Zealand Journal of Obstetrics and Gynaecology. 2003, 43: 307-311. 10.1046/j.0004-8666.2003.00079.x.
Tyzack K, Wallace E: Down syndrome screening: What do health professionals know? . Australian and New Zealand Journal of Obstetrics and Gynaecology. 2003, 43: 217-221. 10.1046/j.0004-8666.2003.00070.x.
Nagle C, Lewis S, Meiser B, Metcalfe S, Carlin J, Bell R, Gunn J, Halliday J: Evaluation of a decision aid for prenatal testing of fetal abnormalities: a cluster randomised trial . BMC Public Health. 2006, 6: 96-10.1186/1471-2458-6-96.
Nagle C, Gunn J, Bell R, Lewis S, Meiser B, Metcalfe S, Ukoumunne OC, Halliday J: Use of a decision aid for prenatal testing of fetal abnormalities to improve women’s informed decision making: A cluster randomised controlled trial . BJOG. 2008, 115 (3): 339-347. 10.1111/j.1471-0528.2007.01576.x.
Stewart D: Focus groups: Theory and practice. 1990, Newbury Park , Sage
Patton M: Qualitative Evaluation and Research Methods. 1980, Newbury Park , Sage, 2nd
Greenwood J, Parsons M: A guide to the use of focus groups in health care research: Part 2. Contemporary Nurse. 2000, 9: 181-191.
Glaser BG, Strauss AL: The Discovery of Grounded Theory: Strategies for Qualitative Research. 1973, Chicago , Aldine
Miles MB, Huberman AM: Qualitative data analysis: An expanded sourcebook. 1994, London , Sage, 2nd
Riley M, Davey MA, King J: Births in Victoria 2003-2004. 2005, Melbourne, Perinatal Data Collection Unit, Public Health, Victorian Government Department of Human Services , Report No.: ISBN: 0731162250, [http://www.rcog.org.uk/resources/public/pdf/down_syndrome_screening.pdf]
Calman KC, Royston GHD: Risk language and dialects. British Medical Journal. 1997, 315 (7113): 939-942.
Stewart M, Weston WW, Brown JB: Patient-Centered Medicine: Transforming the Clinical Method. 1995, Thousand Oaks , Sage
Williams C, Alderson P, Farsides B: Too many choices? Hospital and community staff reflect on the future of prenatal screening. Social Science and Medicine. 2002, 55 (5): 743-753. 10.1016/S0277-9536(01)00200-3.
Green JM: Serum Screening for Down's syndrome: Experience of obstetricians in England and Wales. British Medical Journal. 1994, 309: 769-772.
Muggli E, Halliday J: Prenatal diagnostic testing and Down syndrome in Victoria 1992-2002. Aust N Z J Public Health. 2004, 28 (5): 465-470.
Kennedy A: Supervision for practicing genetic counselors: An overview of models. Journal of Genetic Counseling. 2000, 5.
The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1472-6963/8/114/prepub
This study was funded by Project Grant ID 237124 from the National Health and Medical Research Council, Australia. Bettina Meiser and Jane Halliday are supported by Career Development Awards from The National Medical Research Council of Australia (IDs 350989 & 216741 respectively). We acknowledge the contribution of the other ADEPT project team members: Sylvia Metcalfe and John Carlin. We are most grateful to the anonymous reviewers and all GPs who participated in the study.
The authors declare that they have no competing interests.
CN, SL and RB generated the research question. BM provided expertise on methodology. SL and CN conducted the focus groups. CN, SL conducted the coding and analysis with supervision from and RB. JH and JG provided expertise in interpretation of the results. CN wrote the first draft and all other authors contributed to subsequent drafts and approved the final version.
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Nagle, C., Lewis, S., Meiser, B. et al. Exploring general practitioners' experience of informing women about prenatal screening tests for foetal abnormalities: A qualitative focus group study. BMC Health Serv Res 8, 114 (2008). https://0-doi-org.brum.beds.ac.uk/10.1186/1472-6963-8-114
- Focus Group
- Down Syndrome
- Screen Test
- Extrinsic Factor
- Prenatal Testing