The development and application of a new tool to assess the adequacy of the content and timing of antenatal care
- Katrien Beeckman1Email author,
- Fred Louckx†1,
- Godelieve Masuy-Stroobant†2,
- Soo Downe†3 and
- Koen Putman†4
© Beeckman et al; licensee BioMed Central Ltd. 2011
Received: 3 January 2011
Accepted: 6 September 2011
Published: 6 September 2011
Current measures of antenatal care use are limited to initiation of care and number of visits. This study aimed to describe the development and application of a tool to assess the adequacy of the content and timing of antenatal care.
The Content and Timing of care in Pregnancy (CTP) tool was developed based on clinical relevance for ongoing antenatal care and recommendations in national and international guidelines. The tool reflects minimal care recommended in every pregnancy, regardless of parity or risk status. CTP measures timing of initiation of care, content of care (number of blood pressure readings, blood tests and ultrasound scans) and whether the interventions were received at an appropriate time. Antenatal care trajectories for 333 pregnant women were then described using a standard tool (the APNCU index), that measures the quantity of care only, and the new CTP tool. Both tools categorise care into 4 categories, from 'Inadequate' (both tools) to 'Adequate plus' (APNCU) or 'Appropriate' (CTP). Participants recorded the timing and content of their antenatal care prospectively using diaries. Analysis included an examination of similarities and differences in categorisation of care episodes between the tools.
According to the CTP tool, the care trajectory of 10,2% of the women was classified as inadequate, 8,4% as intermediate, 36% as sufficient and 45,3% as appropriate. The assessment of quality of care differed significantly between the two tools. Seventeen care trajectories classified as 'Adequate' or 'Adequate plus' by the APNCU were deemed 'Inadequate' by the CTP. This suggests that, despite a high number of visits, these women did not receive the minimal recommended content and timing of care.
The CTP tool provides a more detailed assessment of the adequacy of antenatal care than the current standard index. However, guidelines for the content of antenatal care vary, and the tool does not at the moment grade over-use of interventions as 'Inappropriate'. Further work needs to be done to refine the content items prior to larger scale testing of the impact of the new measure.
The use of antenatal care is considered important in preventing adverse pregnancy outcomes. An association between late initiation of antenatal care or receiving few antenatal visits (< 5) and preterm birth [1–3] or low birth weight [2, 4, 5] was found in several studies. Other studies however showed that a reduced number of antenatal visits had no influence on birth outcome, as long as effective and appropriate screening, preventive or treatment interventions were taken [6–8].
The term 'adequacy of care' is not uniformly defined. It can include the number of visits [2, 9, 10], initiation of care [11–13] or continuity of health care provider [14, 15]. Furthermore, indices to measure the adequacy of antenatal care trajectories have been conceptualised in different ways. This leads to variations in definitions of the 'adequacy' criteria. The most currently-used indices are the Adequacy of Prenatal Care Index (APNCU) [16, 17] and the Graduated Index of Prenatal care Utilization (GINDEX) [18, 19]. In both indices, 'adequate care' is defined by the number of consultations adjusted for month when care began and the expected number of visits, adjusted for gestational age at delivery.
Variations in the definition of adequate antenatal care among the different indices lead to different interpretations of results. Furthermore, there is no consensus about the quantity of care a woman should receive , especially because one can receive the same content of care in a smaller number of visits . Different authors [19, 21] suggested that more comprehensive indices are needed. In addition to measuring the number of visits, qualitative aspects of antenatal care use should also be incorporated, such as indicators of content. Refinement of these indices are likely to result in improved tools for monitoring the care women receive and in better evaluation of compliance with recommended standards. More refined indices should further describe specific antenatal care patterns and provide a more accurate tool to evaluate current health policies and program interventions [22, 23].
This study aimed to provide a first step in the development of a more comprehensive tool in which content and timing of antenatal care are considered. The tool was then compared with the currently used APNCU index.
Selection of indicators to measure content of antenatal care
In order to decide which elements of content of care should be considered, we determined that they needed to be easily and unambiguously identifiable and measurable, and based on the existing evidence for the clinical components of antenatal care that are currently used in many countries and settings. To assess the latter, we looked at the evidence for the following commonly used measures and interventions in pregnancy: evaluation of weight gain; fundal health measurement; routine urine testing for glucose and proteinurea; blood pressure measurement; ultrasound screening for gestational age and for fetal abnormalities; blood tests for anaemia, and for maternal infections that can be transmitted to the fetus/baby. This was not an exhaustive list. At this stage, it was determined that the tool would track three or four key elements of care to see if this altered the definition of adequate care when compared to the standard APNCU measure based on quantity of visits alone.
Thorsdottir et al.  demonstrated that evaluation of weight gain during pregnancy can be a predictor of preterm birth, birth weight, macrosomia, large for gestational age babies and small for gestational age (SGA) babies. Further, routinely measuring fundal height seemed not very effective to detect small and large babies . Also the accuracy of routine urine testing for glucose and protein in screening for diabetes or preeclampsia does not seem to be high in clinical practice . In order to detect diabetes, a routine oral 50-g glucose challenge test was superior . Carefully monitoring blood pressure improved the diagnosis and successful treatment of preeclampsia .
Other routine interventions such as ultrasound screening in the first trimester are effective in assessing gestational age accurately, in detecting twin pregnancies and, combined with serum screening markers, in screening for Down's syndrome (nuchal translucency scan) [28–30]. An ultrasound scan in the second trimester (18 to 23 weeks) is an effective method to detect structural anomalies [29–31].
Screening for anaemia in pregnancy appears to be a valid intervention, because low and very high levels of haemoglobin are related to increased risks of poor outcome for mother and baby [32–34]. Blood tests to screen for Hepatitis B  and Human Immunodeficiency Virus  infections are effective and can lead to the prevention of mother-child transmission during childbirth , and the initiation of postnatal treatment or vaccination.
To check if these components had widespread support as effective components of antenatal care, we looked at differences in current guidelines between European countries as well as the recommendations of the World Health Organisation and American guidelines. Many guidelines advise the evaluation of weight gain at every visit [38–41], however guidelines are not congruent because some guidelines only suggest measuring weight at the first visit [42, 43]. In most guidelines a urine test for proteinuria [39, 40, 44] is advised at every visit, while some guidelines do not advise checking for proteinuria during pregnancy [38, 43]. Measurement of fundal height is not always included in the guidelines , and where advised, the timing of commencement varies [38–40, 42–44]. Recommendations on screening for gestational diabetes range from universal screening , over-screening in some populations [39, 40, 44] to no screening at all [42, 43]. All of these guidelines advise one blood test at the beginning of pregnancy [38–40, 43–46]. A second blood screening is advised in most guidelines [39, 40, 42–44]. Almost all guidelines advise the measurement of blood pressure at every visit [38–40, 42, 44]. The recommendations on ultrasound use vary between countries. The World Health Organization and the American College of Obstetrics and Gynecologists (ACOG) do not recommend systematic ultrasound in pregnancy unless it is indicated [39, 42]. All other guidelines advise at least one ultrasound between weeks 18 and 22 to check for fetal anomalies. Fetal aneuploidy screening between weeks 10 to 13 of gestation is advised in several guidelines [40, 43, 44].
The previous steps indicated that, despite being nominally based on current best evidence, guidelines are inconsistent. However, after weighing up the clinical evidence and the European guideline recommendation congruence, we decided to focus on blood pressure (BP), blood screening (BS) and ultrasound screening (US) as valid clinical components for the first iteration of the Content and Timing of care in Pregnancy (CTP) tool. We are aware that future iterations of the tool will require a further scrutiny of this evidence, and that this future work would benefit from consensus methods such as a Delphi study among relevant stakeholders. This study was designed to test the feasibility of using such a tool in principle, before undertaking these refinements in future.
Timing of care in the CTP and definition of categories
The CTP tool classifies care into a four category ordinal scale; inadequate, intermediate, sufficient or appropriate. The tool aimed to reflect if women received a minimum care package recommended in every pregnancy, regardless of parity or risk status. Given the international consensus that care should start by the time of the fourteenth week of gestation [20, 38, 44, 46], we decided to incorporate timely initiation of care as an element in the tool. We also added the timing of the three chosen interventions during the course of the pregnancy.
In the CTP, care trajectories are first assessed against the timing of initiation of care. Women who first receive care after fourteen completed weeks of gestation are automatically assigned to the inadequate category. The care for the remaining women is then measured against the number of times they receive each element of care over the whole care trajectory. The number of actions for each of the three interventions (US, BP, BS) over the whole pregnancy is calculated. Women join the 'inadequate' category when at least one intervention occurred less than the minimum recommended number of times and the number of the other interventions does not exceed the respective ranges (for example 2 US, 1 BP and 1 BS). When at least one intervention occurred less than the minimum recommended number of times but another exceeded the respective ranges the women is assigned to the intermediate group, for example she received 8 US, 1 BP and 1 BS.
For all women that meet the minimum recommended number of interventions, meaning at least 6 BP and 2 BS and 2 US throughout pregnancy and therefore belonging to the 'sufficient' group, the timing of the interventions in pregnancy is considered. When the minimum number of actions for each intervention all occurred in the relevant trimesters, a woman is classified to the 'appropriate' category. When the time criterion for all three interventions is not fulfilled these women stay in the 'sufficient' group.
Women in the 'appropriate' category received the minimal care package recommended for each pregnancy (independent of risk status or parity). For example, women reaching this stage who, during the first trimester had at least one US, BP and BS, during the second trimester at least one US and two BP measurements, and, during their third trimester, at least three BP measurements and one BS, would be allocated to the 'Appropriate' category.
Composition of the APNCU index
The APNCU index was used as the comparator for this study. It takes into account the timing of initiation of care and received number of visits. The index is based on the guidelines for antenatal care use of the ACOG for low risk pregnancies . The APNCU index leads to four categories. The 'inadequate' category includes those women where initiation of care took place after the 4th month (late initiation) or where fewer than 50% of the recommended visits were undertaken. Women starting care before the 4th month and attending between 50-79% of the recommended number of visits are assigned to the 'intermediate' category. Initiation of care before the 4th month and attending 80-109% of the recommended visits assigns women to the 'adequate' group. The 'adequate plus' group contains women starting care before the 4th month of gestation and attending more than 110% of the recommended visits . This measure does not see over-provision as inadequate or inappropriate.
As the current study was undertaken in Belgium, in order to compare the CTP classification with the APNCU index, the APNCU index was adapted from the number of visits recommended by the ACOG to the recommended number of visits within the Belgian guidelines. In this way the effect of the discrepancy between the recommended number of visits in both countries was nullified.
Setting, study design and participants
In order to map antenatal care use, a prospective observational study was conducted in nine out of eleven medical centres that provide antenatal care in the Brussels Metropolitan Region. In Brussels, irrespective of the type of health care provider that provides antenatal care, all women are referred to one of these centres for their ultrasound scan(s). Women were recruited consecutively between April and July 2008 and included if they were aged over eighteen, residing in the metropolitan region, with a gestational age less of than sixteen weeks, or if they were attending the third antenatal visit or less (visits prior to inclusion were documented at intake). Women were excluded if they had a multiple pregnancy, a medical problem (heart disease, diabetes, hypertension or renal disease for instance), were not reachable by phone or did not give informed consent.
Women were asked to document their ongoing antenatal care by documenting the following for each antenatal visit: place of the visit, person visited, date of the visit, visit scheduled or not, reason for the visit and received interventions during that visit (including weighing, measuring blood pressure, urine test, ultrasound, blood screening, vaginal exam, sugar test,...). A diary was developed to record each antenatal visit in a standardised manner and a protocol was developed to explain to the women how to use the diary. Use of a diary enabled us to record also these interventions next to those made by the regular care provider. Bimonthly telephone follow-up interviews were conducted to record received antenatal care, to reduce recall bias and to verify the completeness of the data. Women had the choice of being called in one of five languages: Dutch, French (two of the official languages), English, Turkish or Arabic (foreign languages currently mostly spoken in Brussels). It was estimated that 95.5% of the population speaks one of those five languages . Intercultural workers conducted the interviews limiting cultural barriers.
We undertook a pilot study (unpublished) that demonstrated that the three interventions selected were easily identified by the women and therefore could be reliably collected via a self-report approach. Data from the pilot study was used as training set to test the algorithm of the CTP tool.
Characteristics of the study population and their antenatal care use were described using descriptive statistics. Then the number of women in each category for each tool was compared using Chi2 analyses. Data were managed and analyzed with SPSS 17.0.
The principles of the Helsinki Declaration were taken into account. Written, informed
consent was obtained from all participants. The study was approved by all participating sites and by the Ethics Committee of the University Hospital UZ Brussel.
Characteristics of the study population and received antenatal care
Characteristics of the study population and received antenatal care (N = 333)
No higher education
Active in the labour market
Not active in the labour marked
Characteristics of received antenatal care
(mean ± SD)
Weeks of gestation at initiation of care
Total number of antenatal consultations
Total number of ultrasounds
Total number of blood samples taken
Total number of blood pressure measurements
Weeks of gestation at delivery
Table 1 also shows characteristics related to care during pregnancy. Half of the women initiated care at seven weeks of gestation (P25-P75: 6-10), initiation ranged from 0 to 28 weeks of gestation (results not shown). For interventions during pregnancy, we found that half of the women received five ultrasounds (P25-P75: 4-7), eight blood screenings (P25-P75: 6-10) and eight blood pressure measurements (P25-P75: 6-9). Furthermore, half of the women gave birth at 40 weeks of gestation (P25-P75: 38-40). Women in our sample had more ultrasounds (5.9 compared to 4.1) and slightly more blood tests (4.6 compared to 4.1) compared with the latest regional data (2005) . However some interventions, especially the ultrasounds, are not always charged by the health care provider and therefore not included in the national data.
Comparison of the category distributions for the CTP tool and the APNCU index
Cases assigned by CTP tool compared to APNCU
N = 34
N = 28
N = 120
N = 151
(N = 8)
(N = 23)
(N = 107)
(N = 195)
In this study we developed a tool for assessing antenatal care use that does not only count the number of visits, but also takes into account elements of content and timing of care. As this version of the CTP tool is based on a elements of a basic care package that are recommended by most European guidelines (independent of parity or risk level), the appropriate care category represents women who received the recommended minimum care. The creation of more unambiguous categories is an advantage compared with the APNCU index.
The comparison between the APNCU index and CTP tool showed that, despite the high total number of consultations, women assigned to the APNCU categories 'adequate' or 'adequate plus', were not always classified in the CTP appropriate category. This is because they did not meet the criteria for the number of all three basic interventions combined, or because of inappropriate timing of one of the interventions. The introduction of the additional criteria in the conceptualisation of the CTP tool appeared to lead to a more meaningful approach than with APNCU when assessing the adequacy of antenatal care.
Comparison of the APNCU and CTP tool
NICE* and National guideline**
Adequate Initiation of Care
Adequate number of visits at term gestation
Adequate content of care
Number and timing of ultrasounds
Number and timing of blood pressure
Number and timing of blood tests
Applicable in high risk pregnancies
Penrod et al.  argued for the importance of fully examining the determinants of inadequate antenatal care. In their systematic review, Rowe et al.  described the need for further research on the relationship between social inequalities and antenatal care pathways . As the CTP tool includes important items in antenatal pathways, it may be of interest to analyze them across social groups. The usefulness of measuring received care through CTP on birth outcome needs further exploration.
The limitations of the study include the fact that, at this point, the CTP tool focuses on three basic interventions during pregnancy. We are aware that antenatal care encompasses more than these three interventions. Other components of antenatal care such as other clinical dimensions, satisfaction, referral, reason for the intervention, quality of actions undertaken, spacing of visits or behaviour counselling are not included in our tool. Although the tool does account for the adverse effect of overprovision of some aspects of care when there is underprovision of other aspects (in the second iteration of the process) it does not yet account for overuse where other aspects are provided at the minimum level. This aspect would need to be calibrated against clinical need for higher risk women. In our study for example, half of the women received at least five ultrasounds, while recommendations for evidence based practice only advise two ultrasounds . A risk assessment score could be introduced to further fine-tune the CTP tool. We invite other researchers to test the reproducibility and usefulness of the CTP classification in other settings and to further explore indicators reflecting content and quality of antenatal care that can be added to the CTP model. A large prospective research study across Europe, including a Delphi study to refine the essential elements of the tool, might establish a comprehensive standard of measuring adequate and effective antenatal care.
As this was a prospective study, no data on women without antenatal care were available. Although the number of women without antenatal care is low in Western countries [1, 51, 52] (1% for Belgium ), this group is at higher risk for adverse outcome . Because special attention is needed for this particular group we advise creation of a CTP no-care group separate from the inadequate care group.
The use of indices is largely dependent on the data available. For example, Kotelchuck  warned about incompleteness of birth certificate data for antenatal care information. The level of detail needed to apply CTP may not be available through standard birth registration forms, requiring additional data collection. However, in some countries, detailed information on antenatal care use is registered, including changes in health care provider (eg the combination of the Medical Birth Register and the data on primary health care visits in Finland, Micronatal® in the Netherlands or the personal medical record in the UK). On the other hand the demand for quality control measures in health care will be accompanied with the recording of different elements of care received. Tools such as the CTP may help decision makers in their choice of what data should be collected in the future.
Apart from taking into account initiation and elements of content and timing of care, the CTP tool appeared to have some other advantages compared with other indices. Its conceptual framework departs from a basic timing and quantity measure of care recommended in every pregnancy. It reflects the number and timing of three important interventions during pregnancy, resulting in a more detailed picture of antenatal care use. The CTP tool provides a refined judgment on the adequacy of received antenatal care, as aspects of content of care are considered. Therefore, CTP may be useful in studies on determinants of inadequate antenatal care use. CTP needs to be seen as a first step and future work it is needed to develop an even more useful tool, incorporating more of the elements of antenatal care that make a different to the health and wellbeing of childbearing women and their offspring.
Details Of Ethics Approval
The procedures of the study received ethical approval from the institutional ethics committee responsible for human experimentation. Approval from the ethical committee Academisch Ziekenhuis - Vrije Universiteit Brussel (UZ-Brussel) (University Hospital - VUB) was received on June 29 2006 (2006/084).
List Of Abbreviations
American College of Obstetrics and Gynecologists
Adequacy of Prenatal Care Index
Content and Timing of care during Pregnancy tool
Graduated Index of Prenatal care Utilization
National Institute for Health and Clinical Excellence
small for gestational age
This study was supported by a grant from the Brussels-Capital Region, for which we want to express our gratitude. We would like to thank the members of our advisory commission for their help and advice in our research project. This commission makes it possible to take underpinned and shared decisions in the research process. The members of this commission are S. Alexander, C. Buekenhout, B. Buysse, G. Masuy-Stroobant, M. De Spiegelaere, V. De Vis, G. Vanbrempt and C. Van Vaerenbergh. This study was made possible thanks to the clinical centres that provided the necessary support and the participation of the pregnant women themselves. Furthermore we want to thank professor Kaufmann for his statistical advice in the development of the CTP classification system.
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- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6963/11/213/prepub