Literature DB >> 26508572

Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy.

Celine Lewis1, Melissa Hill1,2, Heather Skirton3, Lyn S Chitty1,2.   

Abstract

Non-invasive prenatal testing (NIPT) using cell-free DNA for aneuploidy is a highly accurate screening test; however, concerns exist around the potential for routinisation of testing. The multidimensional measure of informed choice (MMIC) is a quantitative instrument developed to assess informed choice for Down syndrome screening (DSS). We have validated a modified MMIC for NIPT and measured informed choice among women offered NIPT in a public health service. The measure was distributed to women recruited across eight maternity units in the United Kingdom who had accepted DSS. Construct validity was assessed by simultaneously conducting qualitative interviews. Five hundred and eighty-five questionnaires were completed and 45 interviews conducted after blood-draw (or equivalent for those that declined NIPT). The measure demonstrated good internal consistency and internal validity. Results indicate the vast majority of women (89%) made an informed choice; 95% were judged to have good knowledge, 88% had a positive attitude and 92% had deliberated. Of the 11% judged to have made an uninformed choice, 55% had not deliberated, 41% had insufficient knowledge, and 19% had a negative attitude. Ethnicity (OR=2.78, P=0.003) and accepting NIPT (OR=16.05, P=0.021) were found to be significant predictors of informed choice. The high rate of informed choice is likely to reflect the importance placed on the provision of pre-test counselling in this study. It will be vital to ensure that this is maintained once NIPT is offered in routine clinical practice.

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Mesh:

Year:  2015        PMID: 26508572      PMCID: PMC4867447          DOI: 10.1038/ejhg.2015.207

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


Introduction

In most developed countries it is now routine practice to offer pregnant women Down syndrome screening (DSS) followed by invasive testing for definitive diagnosis for those women at increased risk.[1] The limitations of this approach are that DSS currently has a detection rate (DR) of ~80–90% and a false-positive rate (FPR) of 3–5%,[2] and invasive testing through chromosome analysis of amniocytes or chorionic villus samples carries a procedure-related miscarriage risk of 0.5–1%.[3] Following the identification of cell-free DNA in the maternal plasma in the late 1990's[4] together with the technological advances delivered by next-generation sequencing, it has become possible to offer non-invasive prenatal testing (NIPT) for aneuploidy. It has been clinically available in the private sector since 2011, and is currently being evaluated for use within several publicly funded health-care systems.[5, 6, 7] It has high DRs and low FPRs for Down syndrome (99.0% DR; 0.08% FPR) as well as trisomies 18 (92.1% DR; 0.20% FPR) and 13 (88.6%DT; 0.12F PR),[8] but as NIPT requires confirmation through invasive testing it is considered to be an advanced screening test.[9] The clinical advantages of NIPT are the reduced need for invasive testing, and the opportunity for earlier reassurance as NIPT can be conducted from 10 weeks gestation. Concerns around routinisation of testing because of the ease with which this near-diagnostic test can be conducted have also been raised.[10, 11] Consequently, much discussion has centred around the importance of non-directive counselling and ensuring informed choice when offering NIPT.[1, 9] As such, any evaluation of implementing NIPT into clinical practice should include an assessment of whether women are making informed choices. There is a consensus in clinical guidelines published in the United Kingdom, United States of America and elsewhere that prenatal testing services should facilitate women to make informed choices.[12, 13, 14] Although numerous definitions of informed choice exist,[15, 16, 17] how to assess informed choice has been widely debated and several validated measures have been developed.[17, 18, 19] One of the most accepted quantitative measures is the Multidimensional Measure of Informed Choice (MMIC),[17, 20] which is based on a definition of informed choice being one made with sufficient knowledge, in line with the persons values and attitudes to testing, and behaviourally implemented. The MMIC was originally developed for women undergoing DSS,[20] but has been adapted for other conditions including screening for thalassaemia and sickle cell,[21] fragile X syndrome[22] and cancer.[23] Our aim was to validate a modified MMIC instrument for NIPT and measure informed choice among women offered NIPT following DSS in a public health service.

Materials and methods

We describe the development of a modified MMIC as a measure of informed choice for women offered NIPT for aneuploidy following DSS. This work forms part of a larger study (The NIPT Evaluation Study) evaluating the implementation of NIPT within the National Health Service (NHS) (www.rapid.nhs.uk/).[5] NHS Research Ethics Committee approval was obtained (London – Camden and Islington 13/LO/0082) in February 2013.

Adaptation of MMIC

The original MMIC comprised a knowledge scale, scored as good or poor knowledge, and an attitude scale, scored as positive or negative attitude, which was then combined with test behaviour to determine whether an informed choice had been made.[17] To refine the MMIC for use with NIPT a multidisciplinary expert panel was established to assist in this process. They comprised a specialist in fetal medicine and NIPT, a genetic counsellor with expertise in developing competences for health professionals, the Associate Director of the NHS Genetics and Genomics Education Centre, a research genetic counsellor, two research midwives and representatives from the patient organisations Antenatal Results and Choices and Genetic Alliance UK.

Knowledge scale

Adaption of the MMIC requires the development of a knowledge scale specifically for the condition and screening test being used. An initial set of 11 knowledge items for NIPT were generated by CL. These were informed by previous qualitative interviews exploring patient's informational needs regarding NIPT,[11] a patient information leaflet developed by the expert panel for use in the Evaluation Study, clinical guidelines for offering NIPT[1, 24] and questions used in the original MMIC knowledge scale.[17] The knowledge items were designed to cover following four domains: (1) characteristics of NIPT, (2) how NIPT compares with standard DSS, (3) implications of testing and (4) knowledge about condition(s) for which testing is being offered. These were presented in a multiple choice format with a range of three to six potential choices. To refine the knowledge items, a series of consultations were conducted with the members of the expert panel. During the first round of consultation, the expert panel was asked to rate each knowledge item on a scale of 1–5 (1=not at all, 5=extremely) in terms of both the importance and difficulty. The panel was also asked whether any important questions were missing. Following consultation, some questions were reworded and one additional question was included to address participants' understanding of a ‘highly unlikely' NIPT result. During the second round of consultation the panel was again asked to rate the importance and difficulty of each question. No further amendments to the questions were made. As there is no external criteria for what constitutes ‘good' or ‘poor' knowledge, the panel agreed a cutoff of ≥9/12 would constitute good knowledge. In addition, it was agreed that the responder had to answer the question about what condition(s) NIPT was testing for correctly as this was considered crucial to making an informed choice.

Attitude scale

The items for inclusion into the attitude scale were also subject to a round of consultation with the expert panel. It was agreed to include three of the four items used in the original MMIC scale[17] (beneficial/harmful; important/unimportant; good thing/bad thing), which had been validated in the prenatal setting.[20] However, there was consensus that the fourth item (pleasant/unpleasant) did not represent an important aspect of women's attitude towards NIPT because women have many blood tests during pregnancy. The panel agreed to include two other items, desirable/undesirable and reassuring/not reassuring, which had been validated in other modified MMIC scales.[25, 26] The expert panel was asked to agree a cutoff for the attitude scale. The options included the midpoint of the scale (≥11, range 0–20) in line with the original application of the MMIC attitude scale[20] or an alternative cutoff used by Van den Berg and colleagues[27] in which attitude is scored into three equal categories (positive, neutral and negative) and people with a neutral attitude are removed from the informed choice calculation. The expert panel unanimously agreed on the Van den Berg approach.

Deliberation scale

Deliberation is considered to be a key component of the decision-making process in many health behaviour theories,[28, 29] and a deliberation scale has been included alongside the original MMIC in a previous study measuring informed choice in prenatal screening.[30] The panel agreed to include the deliberation scale in the questionnaire and the results of informed choice are presented both with and without this scale.

Piloting the questionnaire

In the final stage of development the MMIC was piloted with 20 women who had been offered NIPT as part of the NIPT Evaluation Study. A researcher (CL) then conducted a short face to face interview with each responder to assess the clarity of question and answer options. Some minor modifications to wording were made. The questionnaire including the final MMIC scale is included in the Supplementary Information.

Study procedure

A protocol detailing recruitment into the Evaluation Study has been published.[5] In brief, women were recruited through one of eight antenatal clinics located across the United Kingdom, which varied in terms of the demography of their catchment areas. Women were eligible to participate if they had accepted DSS as part of routine care, were older than 16 years, had a singleton pregnancy and able to read and understand English (owing to resource constraints we were unable to translate the information materials and questionnaire) and provide informed consent. Those with an intermediate (1:1000–1:151) or high-risk result (1:150–1:2) following DSS were invited into the Evaluation Study and offered NIPT free of charge. Women with an intermediate risk DSS result were offered NIPT or no further testing; women with a high-risk DSS result were offered NIPT, invasive testing, NIPT and invasive testing or no further testing. All women received individualised pre-test counselling with a dedicated NIPT research midwife as well as written information about NIPT at two time points (booking-in and pre-test counselling) prior to decision-making. Information given to women during pre-test counselling is summarised in Figure 1. A subset of women eligible for the Evaluation Study was invited to take part in the Informed Choice study. Women were recruited as a consecutive sample between December 2013 and February 2015. This was a longitudinal cohort study involving questionnaires and interviews at two time points. Only questionnaire and interview responses from the first time-point (T1) are presented here as these relate directly to validation of the amended MMIC.
Figure 1

Information provided to participants about NIPT.

Questionnaires

The first questionnaire (Q1) was given to women after blood had been taken (or within a similar timeframe for women who declined testing). Q1 contained the modified MMIC as well as: The Decisional Conflict Scale;[31] the short form of the State Trait Anxiety Inventory (STAI-6);[32] questions to explore motivations for testing and preference for test attributes; questions on parity and socio-demographic questions (Table 1). The results from these additional questions are presented in a forthcoming paper (‘Women's experience of being offered NIPT for aneuploidy in a national health service setting' manuscript in preparation). Participants were requested to leave their contact details so that a follow-up questionnaire could be sent and indicate their willingness to take part in an interview. We aimed to collect at least 50 completed questionnaires from women seen consecutively at each of eight participating maternity units. On the basis of the results of the informed choice study by Michie et al.[20] a sample of 350 completed questionnaires would detect a difference of 10% in rates of informed choice with 97% power at the 5% level of significance.
Table 1

Participant characteristics

Participant characteristicsN=585
Maternal age—mean, (IQR)35 years (32–39)
  
Educational level
 No qualification1% (n=6)
 GCSE or O level8% (n=44)
 GCE, a level or similar8% (n=46)
 Vocational (BTEC/NVQ/diploma)19% (n=111)
 Degree level or above64% (n=371)
  
Ethnicity
 White or White British77% (n=438)
 Asian or Asian British11% (n=62)
 Black or Black British7% (n=39)
 Other ethnic group3% (n=17)
 Mixed3% (n=15)
  
Religious faith
 Yes53% (n=302)
 No47% (n=271)
  
Religion
 Christian75% (n=232)
 Muslim12% (n=38)
 Jewish5% (n=15)
 Other3% (n=8)
 Sikh2% (n=7)
 Hindu2% (n=7)
 Buddhist1% (n=3)
  
Religiosity
 Very20% (n=50)
 Somewhat66% (n=163)
 Not at all14% (n=34)
  
DSS risk
 Intermediate risk72% (n=421)
 High risk28% (n=163)
  
Further testing
 NIPT94% (n=548)
 NIPT and invasive testing4% (n=24)
 No further testing2% (n=13)
  
NIPT on same day or different day as DSS
 Different day62% (n=357)
 Same day35% (n=200)
 Same day but chose to return4% (n=21)
  
Parity
 Parous54% (n=306)
 Nulliparous47% (n=266)
  
DSS in previous pregnancy
 Yes75% (n=240)
 No23% (n=73)
 Not sure3% (n=9)
  
Have a child with Down's syndrome
 Yes<1% (n=1)
 No99.7% (n=329)
Know a child with Down's syndrome
 Yes29% (n=164)
 No71% (n=393)

Note: not all % add up to 100 owing to rounding. Not all participants answered all questions, and therefore there are some discrepancies with total numbers.

Interviews

Semi-structured interviews were conducted with a subset of women. The interviews included questions drawn from the concepts of the MMIC (knowledge, attitude and deliberation). Construct validity of the measure was assessed by comparing women's scores on the questionnaire with their responses during interview. Interviews were also used to validate the cutoff for good knowledge. In asking women to recount what information they remembered being given about NIPT, the aim was not only to assess recall of information but also ensure understanding of the implications of the test. Women's attitudes towards NIPT were assessed by exploring their reasons for accepting or declining testing, and the values underpinning those attitudes. Deliberation was assessed by exploring whether they had considered the possible consequences of NIPT or evaluated alternative options. Participants were purposively sampled to represent a range of demographic groups (educational level, ethnicity, religion and religiosity), testing choices, MMIC scores and test outcomes. Interviews were conducted until saturation was reached.

Data analysis

Analysis of the MMIC

To assess informed choice, knowledge scores (which were dichotomized as good or poor), attitude scores (which were classified as positive, negative or neutral with neutral responders being omitted) and deliberation scores (which were dichotomized as deliberated or non-deliberated) were combined with test behaviour. When participants had good knowledge, had deliberated, and if attitude was consistent with test uptake, an informed choice had been made. If knowledge was poor, the choice was not deliberated or if attitude was not consistent with test uptake, an uninformed choice had been made. Reliability of the knowledge, attitude and deliberation scales was assessed using Cronbach's alpha, which measures internal consistency. Alpha values of 0.7–0.9 are assumed to indicate good internal consistency.[33] Construct validity of the adapted attitude scale was also measured using factor analysis to determine whether the items spanned one or more dimensions.[34] To validate the cutoff for good knowledge women's mean knowledge scores were compared using the t-test. To look at the impact of socio-demographic variables on informed choice, descriptive analysis was conducted on single items; relationships between groups were tested using χ2-tests and Fisher's exact test for categorical variables and the Kruskal–Wallis test for continuous variables. Owing to the dominance of one category in the variables education, ethnicity and religion, the categories were collapsed into binary categories to strengthen the analysis, ie, White ethnicity vs other, degree education or higher vs other, Christian vs other. Logistic regression analysis was conducted to determine, which independent variables were significant predictors of informed choice. Missing data on the knowledge scale were treated as incorrect answers. Questionnaires with missing data on the attitude and knowledge scale were removed from analysis as they prohibited calculation of informed choice. Data were analysed using SPSS 22 (IBM, Chicago, IL, USA).

Analysis of qualitative interviews

Construct validity of the MMIC was also assessed by comparing results of the component scales with qualitative responses from interviews. This validation process was undertaken by two researchers independently (CL and MH). Qualitative data were independently coded by CL and MH to score knowledge (good or poor), attitude (positive, negative or neutral) and deliberation (deliberated or non-deliberated). The results were compared following independent analysis and any discrepancies discussed until consensus was reached. For each participant the assessment of whether an informed choice had been made was then compared back to the assessment made via the MMIC.

Results

Participant characteristics

In total, 731 women were invited to take part in the Informed Choice study and 593 agreed to participate and completed Q1 (81% response rate). During the first phase of data analysis, eight questionnaires were removed due to missing data (N=585). A summary of maternal characteristics are presented in Table 1. Regarding DSS risk, 72% of women had an intermediate risk and 28% were high risk. Regarding NIPT uptake, in the intermediate risk group (n=421), 97% chose NIPT and 3% chose no further testing. In the high-risk group (n=163), 86% chose NIPT and 14% chose NIPT and invasive testing. We do not have demographic or testing decision data for participants who declined to participate in the Informed Choice study.

Internal reliability

The alpha coefficients for the knowledge, attitude and deliberation scales indicated internal reliability (Table 2). The screening test for the factor analysis showed an elbow between factors 1 and 2. The factor, with an eigenvalue of 4.12, accounted for 82% of the variability across the five items of the attitude scale, indicating construct validity.
Table 2

Summary of multidimensional measure of informed choice

MeasureDescriptionItemsReliabilityaRangeCutoffMean (SD)Outcome
Knowledge scaleKnowledge of NIPT, how it compares with standard DSS, options if the NIPT result is positive, knowledge about Down syndrome12 questions, multiple choice answers0.690–12≥9=good knowledge11.1 (1.5)Good knowledge: 95%
Attitude scaleAttitude towards having NIPTFive 5-point Likert items0.940–200–6=positive 7–13=neutral 14–20=negative2.2 (3.7)Positive: 88% Negative: 2% Neutral: 10%
Deliberation scaleEvaluating alternatives, considering consequences, weighing up pros and consSix 5-point Likert items0.840–240–12=deliberated5.2 (5.0)Deliberated: 92%
UptakeWhether NIPT was accepted or declinedChoice of 4 options: NIPT, no further testing, straight for invasive, invasive and NIPTNIPT: 94% NIPT and invasive: 4% No further testing: 2%
Informed choicebGood knowledge, deliberated, attitude and behaviour match.CalculatedInformed choice: 89% inc. deliberation 94% excl. deliberation

Abbreviation: DSS, Down syndrome screening.

Reliability was assessed using Cronbach's alpha.

Calculation does not include women with a neutral attitude.

Construct validity

Forty-five interviews were conducted with women at T1 to assess and explore knowledge, attitude and deliberation. Forty-three women were judged to have good knowledge (96%), 41 were judged to have a positive attitude (91%) and 44 were judged to have deliberated (98%). Example quotes illustrating knowledge, attitude and deliberation are presented in Table 3. The interview assessment of informed choice was then compared with the corresponding questionnaire. Overall, five (11%) discrepancies were identified; in two cases these related to attitude, in two cases deliberation, and in one case a discrepancy was found for both deliberation and knowledge. In each case the participant had failed to reach the required cutoff on the questionnaire but had displayed adequate knowledge, a positive attitude and deliberation during the interview. The knowledge scores were significantly higher in women judged at interview to have good knowledge (M=11.12, SD=1.31) compared with those judged to have poor knowledge (M=6; SD=1.41), suggesting the cutoff for what constitutes good knowledge was appropriate (t(43)=5.38, P<0.001).
Table 3

Illustrative quotes of knowledge, attitude and deliberation

DomainIllustrative quote
Good knowledge‘She said it was non-invasive so it wouldn't harm the baby at all, it was just a blood test...If it was ‘highly likely' I would be offered an invasive test that would give me a definite answer if it was Down's syndrome' 31 years, low risk and had NIPT
Poor knowledge‘We could get the results much quicker than an amnio. It's somewhat more accurate I think than the CVS.' 39 years, high risk and had NIPT
Positive attitude‘I think I'd just want to be better informed about Down's Syndrome and be prepared for it.' 23 years, high risk and had NIPT
Negative attitude‘The thought of having to make a decision about what to do afterwards…I didn't feel the need to go further down that road' 39 years, low risk and declined further testing
Neutral or ambivalent attitude‘I'm quite happy to help out with studies…I kind of think the more you look the more likely you are to get a result that is unusual, even if it doesn't actually turn out to be something and actually the worry that that causes isn't really worth it… but then still when offered it I still do it! So there's a bit of a discrepancy there between my thoughts and my actions.' 32 years, low risk and had NIPT
Deliberated‘I discussed it with my partner and explained obviously what it was and, you know, we discussed the pros and cons and really, for us, there were no cons because it was a simple blood test and we just decided that it would be much better to have all the knowledge up front.' 32 years, low risk and had NIPT
Not deliberated‘I just accepted on the spot because I thought well that's brilliant, that's extra information and with no risk, why wouldn't I accept that?' 35 years, low risk and had NIPT ‘Having already decided that I was going to have the combined screen having this one was kind of a no-brainer because it does the same thing only it's better and it doesn't involve any risk'. 38 years, low risk and had NIPT

Informed choice

According to the MMIC, 89% (n=467) of women were judged to have made an informed choice about NIPT. When we excluded the deliberation scale this increased slightly to 94% (n=492). Of the total sample, 95% (n=553) were judged to have good knowledge, 88% (n=513) had a positive attitude (2% had a negative attitude, and 10% had a neutral attitude and were excluded from the informed choice calculation) and 92% (n=539) had deliberated. In all cases apart from one, the informed choices made (when deliberation was included in the measure) were those in which women had good knowledge, a positive attitude, had deliberated on their decision and had undergone testing. In one case a woman had made an informed choice based on good knowledge, deliberation, a negative attitude and had declined invasive testing. Of the 11% (n=58) who were judged to have made an uninformed choice, 55% (n=32) had not deliberated, 41% (n=24) had insufficient knowledge, and 19% (n=11) had a negative attitude (eight of whom accepted NIPT and three of whom declined). Bivariate analysis showed that women found to have made an informed choice were significantly more likely to be: NIPT accepters (OR=5.38, P<0.001), White (X2(1)=12.99, OR=1.15, P<0.001), university educated (X2(1)=4.10, OR=1.07, P=0.043) and high risk (X2(1)=4.082, OR=1.07, P=0.043). There was no significant difference in rates of informed choice across antenatal clinics (P=0.101). Multivariable regression analysis demonstrated that ethnicity and NIPT uptake were significant predictors of informed choice when controlling for education, age, having a religious faith, parity and screening risk. White participants had almost three times higher odds of making an informed choice than other ethnic groups who were more likely to agree to testing despite their beliefs (OR=2.78, 95% CI: 1.42–5.46, P=0.003); NIPT accepters had 16 times higher odds of making an informed choice than NIPT decliners (OR=16.05, 95% CI: 1.53–168.81, P=0.021) although the large confidence interval indicates a low level of precision due to the small number of NIPT decliners in the study (Table 4).
Table 4

Regression analysis for predicting informed choice

Independent variableB(SE)Odds ratio (95% CI)P-value
NIPT accepter2.77(1.20)16.04 (1.53–168.81)0.021*
White ethnicity1.02(0.34)2.78 (1.42–5.46)0.003*
University education0.38(0.32)1.46 (0.77–2.75)0.24
Age0.01(0.03)1.02 (0.96–1.07)0.63
No religious affiliation0.09(0.33)1.10 (0.48–1.74)0.77
High-risk DSS0.48(0.37)1.62 (0.77–3.41)0.20
Nulliparous0.33(0.33)1.39 (0.73–2.66)0.31

Note: *P<0.05; R2=0.07 (Hosmer & Lemeshow), 0.05 (Cox & Snell), 10 (Nagelkerke). Model X2(7)=22.97, P=0.002.

Knowledge, attitude and deliberation scores

A Kruskal–Wallis test revealed significant differences in knowledge and attitude scores and a number of socio-demographic variables. Knowledge scores were significantly affected by education (H(4)=41.99, P<0.001) and ethnicity (H(4)=20.21, P=<0.001). Pairwise comparisons with a Bonferroni correction for multiple comparisons revealed participants with no qualification (U=191.08, P=0.027, r=−0.16), GCSE/O level qualifications (U=119.03, P<0.001, r=−0.15) and vocational qualifications (U=63.86, P=0.001, r=−0.18) had significantly lower knowledge scores compared with those with a university degree; and Asian participants had significantly lower knowledge scores compared with White participants (U=65.64, P=0.012, r=−0.15). Attitude scores were also significantly affected by education (H(4)=9.99, P=0.041) and ethnicity (H(4)=24.43, P<0.001). Pairwise comparisons revealed participants with vocational qualifications had significantly more negative attitudes towards NIPT compared with those with a university degree (U=46.55, P=0.034, r=−0.14); and Black participants had significantly more negative attitudes compared with White participants (U=112.39, P<0.001, r=−0.21). Screening risk was also found to be significantly associated with attitude and deliberation scores; women with a high-risk DSS result had more positive attitudes towards NIPT than those with a low risk result (U=30846, z=−2.15, P=0.032, r=−0.09) and had deliberated more (U=26504, z=−4.33, P<0.001, r=−0.18).

Discussion

This is, to our knowledge, the first adaptation of the MMIC scale for use with women considering NIPT for aneuploidy. The vast majority of participants in this sample were found to have made an informed choice, although we recognise that these results represent data collected in a research project and may reflect the high importance placed on the provision of pre-test counselling as part of the project. These findings do however emphasise the importance of providing pre-test counselling to provide women with sufficient information and support should NIPT be implemented into routine maternity-care pathways. This finding is in stark contrast to previous research on informed choice in DSS,[35] which has generally found rates of informed choice to be low,[17, 26, 36, 37] commonly due to poor knowledge.[19, 36, 37] A further reason for the high rates of informed choice in our sample may be because women with an increased risk result may have found more relevance in their decision to accept or decline NIPT, leading them to becoming more informed. Introducing NIPT for aneuploidy outside of a research setting is likely to result in less time for pre-test counselling specifically around this test, which has the potential to impact on patient knowledge and consequently informed choice. This concern is supported by recent research in the USA with genetic counsellors offering NIPT for aneuploidy, which suggests that a large number of patients do not understand that NIPT is a screening test.[38] If and when the test is adopted into standard maternity-care pathways, evaluation will be needed to confirm whether women are making informed choices. In this study, non-White participants and participants with a lower educational level were significantly less likely to make an informed choice. This is in line with previous research assessing informed choice among women offered prenatal screening in the United Kingdom, where South Asian and Black African Caribbean women and those from low-socioeconomic backgrounds were less likely to make an informed choice than other women.[39] Similarly, in a study conducted in the Netherlands, women of Turkish and Surinamese origin were less likely to make an informed choice than those of Dutch origin.[40] These observations support the theory that health-care systems are less good at facilitating informed choice in the prenatal setting for women from minority ethnic groups and from lower educational backgrounds. This may be for a number of reasons including inequity of access for ethnic minority groups,[41] or that pre-test counselling and/or informed choice measures are too complex for those with low-literacy levels.[42] Our findings suggest that poor knowledge and negative attitudes had a significant role. This emphasises the importance of finding ways to enhance the informed choice process among different cultural and economic groups in order not to exacerbate the health divide, for example through different media formats to enhance understanding or decision aids to help clarify women's attitudes. Further research in this area would therefore be valuable. Interestingly, the greatest number of uninformed choices were made as a result of decisions not being deliberated on. This may be because reporting whether one has deliberated on something is more difficult than reporting on one's knowledge or attitudes, or because women did not necessarily deliberate on the decision to have NIPT because they had already considered DSS and wanted a more accurate assessment of risk. NIPT was essentially a continuation of this pathway. This was a finding that emerged during qualitative interviews. Future use of the Deliberation scale in this context could include rewording so that deliberation encompasses both screening and NIPT. A further reason may be because women do not give full consideration to NIPT because it is a blood test of which there are a number during pregnancy. This is a concern that has been raised previously by both patients and health-care professionals.[11, 43] This emphasises the importance of ensuring that as well as focussing on knowledge, health professionals must encourage patients to consider the implications of the test results, what information would be of benefit to them and what options might be available. We also found that women with a high-risk screening result were more likely to deliberate on NIPT than those with an intermediate risk. This is not unexpected given that that those at a higher risk in this study may be weighing up the option of NIPT against invasive testing and may consider their decision in more depth because of the potential implications; however, this finding does highlight the need for health professionals to ensure women with a DSS risk <1:150 give sufficient thought to the advantages and disadvantages of NIPT, particularly given that there is still a chance, albeit small, that the fetus may be affected. The methodology used to modify the MMIC has a number of notable strengths including the use of qualitative methods to explore the decision-making process, which has provided an additional dimension to the evaluation and validation of the modified MMIC.[44] There was a high concordance between the modified MMIC and the interviews in determining whether an informed choice had been made. However, although overall the modified MMIC appears to be a robust measure of informed choice, like other measures it is not possible to pick up subtle nuances in decision-making that may be evident from qualitative interviews or clinical history. For example, in one case there was a discordant result whereby the questionnaire indicated a non-deliberated decision. However, the interview revealed that the woman had in fact deliberated but that this had occurred much earlier on in the process when considering DSS. For this woman, the decision to have NIPT was an extension of the decision to have screening and she therefore made the decision to accept NIPT relatively quickly and without much consideration. In another case a participant's neutral attitude score was found to most likely stem from a dislike of needles rather than a neutral attitude to NIPT, which she viewed positively as an opportunity for reassurance. A further limitation of the MMIC is that it is unable to account for situations whereby a positive attitude towards NIPT is not behaviourally implemented for practical reasons, eg, being unwilling to return to the clinic for a blood test due to time or cost implications. These findings highlight a potential limitation of the questionnaire in that it is unable to capture the reasons underpinning women's attitudes and highlights the value of a mixed methods approach supported by interviews as in this study. The measure was validated among women considering NIPT as a second screening test following a high- or medium-risk DSS result and not women using NIPT as a first screening test. Further validation would need to take place to use the measure among these different population groups. We were only able to recruit a small number of NIPT decliners (n=13) into the study and of these the vast majority were judged to have made an uniformed choice. However, given the small number, this finding should be interpreted with caution, particularly as others have reported higher rates of informed choice in screening decliners.[19, 27] Our sample predominantly comprised older, well-educated women, however this probably reflects the fact that older women are more likely to be at increased risk and be highly educated as they have delayed child bearing for educational or vocational reasons. Currently, it is not clear whether NIPT will be offered as a contingent screening test or a first-line test offered to all women. Offering NIPT to a wider group of women may impact rates of informed choice and will thus require further assessment. Lastly, the high rate of informed choice may reflect the fact that women were given up to 30 min pre-test counselling with a dedicated NIPT midwife and written information at a number of different points prior to decision-making. This degree of input may be challenging in routine clinical settings, especially if there is not the same emphasis on pre-test counselling, highlighting the need for evaluation following implementation.

Conclusion

We have developed and validated a measure of informed choice for women offered NIPT for aneuploidy, which can be used in other maternity settings. Previous concerns have been raised relating to routinisation of NIPT and erosion of informed choice given the relative ease with which NIPT can be conducted. Whilst recognising that our sample comprised a high proportion of well-educated women, our results indicate that given adequate information, time and expert pre-test counselling a high rate of informed choice can be achieved. Further research as and when NIPT is implemented into routine clinical settings is required.
  35 in total

1.  Presence of fetal DNA in maternal plasma and serum.

Authors:  Y M Lo; N Corbetta; P F Chamberlain; V Rai; I L Sargent; C W Redman; J S Wainscoat
Journal:  Lancet       Date:  1997-08-16       Impact factor: 79.321

2.  A measure of informed choice.

Authors:  T M Marteau; E Dormandy; S Michie
Journal:  Health Expect       Date:  2001-06       Impact factor: 3.377

3.  Low uptake of prenatal screening for Down syndrome in minority ethnic groups and socially deprived groups: a reflection of women's attitudes or a failure to facilitate informed choices?

Authors:  Elizabeth Dormandy; Susan Michie; Richard Hooper; Theresa M Marteau
Journal:  Int J Epidemiol       Date:  2005-02-28       Impact factor: 7.196

Review 4.  Informed choice for screening: implications for evaluation.

Authors:  Les Irwig; Kirsten McCaffery; Glenn Salkeld; Patrick Bossuyt
Journal:  BMJ       Date:  2006-05-13

5.  Informed choice in antenatal Down syndrome screening: a cluster-randomised trial of combined versus separate visit testing.

Authors:  Elizabeth Dormandy; Susan Michie; Richard Hooper; Theresa M Marteau
Journal:  Patient Educ Couns       Date:  2006-04

6.  Accepting or declining the offer of prenatal screening for congenital defects: test uptake and women's reasons.

Authors:  Matthijs van den Berg; Danielle R M Timmermans; Johanna H Kleinveld; Elisa Garcia; John M G van Vugt; Gerrit van der Wal
Journal:  Prenat Diagn       Date:  2005-01       Impact factor: 3.050

7.  Are pregnant women making informed choices about prenatal screening?

Authors:  Matthijs van den Berg; Danielle R M Timmermans; Leo P Ten Kate; John M G van Vugt; Gerrit van der Wal
Journal:  Genet Med       Date:  2005 May-Jun       Impact factor: 8.822

8.  The multi-dimensional measure of informed choice: a validation study.

Authors:  Susan Michie; Elizabeth Dormandy; Theresa M Marteau
Journal:  Patient Educ Couns       Date:  2002-09

9.  The development of a six-item short-form of the state scale of the Spielberger State-Trait Anxiety Inventory (STAI).

Authors:  T M Marteau; H Bekker
Journal:  Br J Clin Psychol       Date:  1992-09

Review 10.  Psychosocial aspects of genetic screening of pregnant women and newborns: a systematic review.

Authors:  J M Green; J Hewison; H L Bekker; L D Bryant; H S Cuckle
Journal:  Health Technol Assess       Date:  2004-08       Impact factor: 4.014

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  25 in total

1.  Patients' Knowledge of Prenatal Screening for Trisomy 21.

Authors:  Michal Sheinis; Kira Bensimon; Amanda Selk
Journal:  J Genet Couns       Date:  2017-07-14       Impact factor: 2.537

2.  The effect of a decision aid on informed decision-making in the era of non-invasive prenatal testing: a randomised controlled trial.

Authors:  Lean Beulen; Michelle van den Berg; Brigitte Hw Faas; Ilse Feenstra; Michiel Hageman; John Mg van Vugt; Mireille N Bekker
Journal:  Eur J Hum Genet       Date:  2016-05-18       Impact factor: 4.246

Review 3.  Prenatal and pre-implantation genetic diagnosis.

Authors:  Joris Robert Vermeesch; Thierry Voet; Koenraad Devriendt
Journal:  Nat Rev Genet       Date:  2016-09-15       Impact factor: 53.242

4.  Education and Consent for Population-Based DNA Screening: A Mixed-Methods Evaluation of the Early Check Newborn Screening Pilot Study.

Authors:  Holly L Peay; Angela You Gwaltney; Rebecca Moultrie; Heidi Cope; Beth Lincoln- Boyea; Katherine Ackerman Porter; Martin Duparc; Amir A Alexander; Barbara B Biesecker; Aminah Isiaq; Jennifer Check; Lisa Gehtland; Donald B Bailey; Nancy M P King
Journal:  Front Genet       Date:  2022-05-12       Impact factor: 4.772

5.  Talking Points: Women's Information Needs for Informed Decision-Making About Noninvasive Prenatal Testing for Down Syndrome.

Authors:  Aimée C Dane; Madelyn Peterson; Yvette D Miller
Journal:  J Genet Couns       Date:  2018-03-17       Impact factor: 2.537

6.  NIPT and Informed Consent: an Assessment of Patient Understanding of a Negative NIPT Result.

Authors:  Julie L Piechan; Karrie A Hines; Daniel L Koller; Kristyne Stone; Kimberly Quaid; Wilfredo Torres-Martinez; Divya Wilson Mathews; Tatiana Foroud; Lola Cook
Journal:  J Genet Couns       Date:  2016-04-01       Impact factor: 2.537

7.  Female and male perspectives on male partner roles in expanded carrier screening.

Authors:  Sarah Jurgensmeyer; Sarah Walterman; Andrew Wagner; Kenny Wong; Annie Bao; Sarah Stueber; Sara Spencer
Journal:  J Assist Reprod Genet       Date:  2021-01-06       Impact factor: 3.412

8.  A qualitative study looking at informed choice in the context of non-invasive prenatal testing for aneuploidy.

Authors:  Celine Lewis; Melissa Hill; Lyn S Chitty
Journal:  Prenat Diagn       Date:  2016-08-23       Impact factor: 3.050

9.  Women's Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods Study.

Authors:  Celine Lewis; Melissa Hill; Lyn S Chitty
Journal:  PLoS One       Date:  2016-04-05       Impact factor: 3.240

10.  Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units.

Authors:  Lyn S Chitty; David Wright; Melissa Hill; Talitha I Verhoef; Rebecca Daley; Celine Lewis; Sarah Mason; Fiona McKay; Lucy Jenkins; Abigail Howarth; Louise Cameron; Alec McEwan; Jane Fisher; Mark Kroese; Stephen Morris
Journal:  BMJ       Date:  2016-07-04
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