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The profiles of public and private patients in maternal healthcare: a longitudinal study to examine adverse selection

Published online by Cambridge University Press:  14 June 2019

Jananie William*
Affiliation:
Research School of Finance, Actuarial Studies and Statistics, Australian National University, Australia2601
Bronwyn Loong
Affiliation:
Research School of Finance, Actuarial Studies and Statistics, Australian National University, Australia2601
Catherine Chojenta
Affiliation:
Research Centre for Generational Health & Ageing, The University of Newcastle, Australia2308
Deborah Loxton
Affiliation:
Research Centre for Generational Health & Ageing, The University of Newcastle, Australia2308
*
*Corresponding author. Email: jananie.william@anu.edu.au
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Abstract

In this article, we investigate differences in the profiles of patients within the Australian mixed public-private maternal health system to examine the extent of adverse selection. There are conflicting influences on adverse selection within the private health sector in Australia due to government regulations that incentivise lower risk segments of the population to purchase community-rated private health insurance. We use a two-phase modelling methodology that incorporates statistical learning and logistic regression on a dataset that links administrative and longitudinal survey data for a large cohort of women. We find that the key predictor of private patient status is having private health insurance, which itself is largely driven by sociodemographic factors rather than health-or pregnancy-related factors. Additionally, transitioning between the public-private systems for a subsequent pregnancy is uncommon; however, it is primarily driven by changes in private health insurance when it occurs. Other significant factors when transitioning to the private system for a second pregnancy are hypertension, increased access to specialists and stress related to previous motherhood experiences. Consequently, there is limited evidence of adverse selection in this market, with targeted financial incentives likely outweighing the impact of community rating even during childbearing years where private health service use increases.

Type
Paper
Copyright
© Institute and Faculty of Actuaries 2019 

1. Introduction

Australia’s maternal healthcare system is composed of mixed public–private service provision and funding arrangements. The overall system is characterised by a predominantly obstetrician-led private system, and a midwife-led or shared-care model with general practitioners in the public system. There are other models of care available in the public system which include the involvement of multidisciplinary obstetric teams if indicated by risk factors or complications (Adams et al., Reference Adams, Tudehope, Gibbons and Flenady2018). Public–private comparisons have shown that there are clear disparities in cost risk factors (William et al., Reference William, Chojenta, Martin and Loxton2018b) and clinical services (Roberts et al., Reference Roberts, Tracy and Peat2000; Shorten & Shorten, Reference Shorten and Shorten2000; Dahlen et al., Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2012, Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2014; Einarsdóttir et al., 2012, Reference Einarsdóttir, Haggar, Pereira, Leonard, de Klerk, Stanley and Stock2013b; Nippita et al., Reference Nippita, Lee, Patterson, Ford, Morris, Nicholl and Roberts2015) with mixed results on how this may impact on neonatal and maternal outcomes (Shorten & Shorten, Reference Shorten and Shorten2002; Robson et al., Reference Robson, Laws and Sullivan2009; Einarsdóttir et al., Reference Einarsdóttir, Kemp, Haggar, Moorin, Gunnell, Preen and Holman2012, Reference Einarsdóttir, Haggar, Langridge, Gunnell, Leonard and Stanley2013a,b,c; Dahlen et al., Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2014; Adams et al., Reference Adams, Gibbons and Tudehope2017, Reference Adams, Tudehope, Gibbons and Flenady2018; Jang et al., Reference Jang, Flatley, Greer and Kumar2017) by system; however, these studies have not investigated the detailed profiles of patients that enter into each system. Furthermore, there have been no studies that directly address the potential for adverse selection in private maternal health services, despite the substantially increased usage of private health insurance (PHI) during childbearing years for women (Australian Prudential Regulatory Authority, 2018). In particular, previous studies do not determine whether women who are at higher risk of pregnancy complications are more likely to take-up PHI and elect private services; or whether high-risk women transition between systems for subsequent pregnancies. A better understanding of the profiles of women in each system will help infer whether adverse selection is evident in the context of this maternal health system.

In Australia, all residents are entitled to free hospital services in the public system under Medicare, a universal government-funded health insurance scheme. All individuals can also elect to use the private system, but the cost-sharing arrangements for the private sector are more complex and likely to involve a combination of individual, government and PHI sources. Individuals with PHI may use this insurance to help fund private services and individuals without PHI largely self-fund private care. It is unlikely that PHI will wholly cover the cost of private hospital services during the perinatal period, so the individual is likely to face out-of-pocket expenses when using private services. The regulation of the Australian system creates an additional layer of complexity in that financial penalties are used to encourage certain groups to purchase PHI. Specifically, the Medicare Levy Surcharge (MLS; introduced in 1997) applies as an additional tax to high-income earners that do not have PHI for hospital treatment and the Lifetime Health Cover (LHC; introduced in 2000) applies a premium loading to individuals who do not purchase PHI before the age of 30 years (Buchmueller, Reference Buchmueller2008; Australian Taxation Office, 2018a,b; The Department of Health, 2018a). A government-funded premium subsidy was also introduced with the MLS to make PHI more affordable and encourage more people into the private system (Australian Taxation Office, 2018b). While these policies may have encouraged 45% of the population to purchase PHI in 2018 (Australian Prudential Regulatory Authority, 2018) and 26% of all hospital births to occur in private hospitals in 2014 (Australian Institute of Health and Welfare, 2018), those with PHI may still elect to be treated as public patients for free under Medicare and thereby avoid any out-ofpocket expenses. Further details of the Australian maternal health system are provided elsewhere (William et al., Reference William, Chojenta, Martin and Loxton2018a,b).

Adverse selection has been widely studied in the insurance literature, and it is well recognised that information asymmetry between insurers and individuals could lead to adverse selection (Hoy & Lun, Reference Hoy and Lun2017; Thomas, Reference Thomas2017). In other words, the potential for individuals to have more information about their own risk profile which is not observable to insurers could lead to higher risks being more likely to purchase the insurance (and conversely, lower risks being less likely to purchase insurance). For PHI specifically, adverse selection may arise if it attracts individuals who believe they are at higher risk of health problems, or in the case of maternal health, at higher risk of pregnancy-or birth-related complications. Although most insurers mitigate the pregnancy risk to some extent by applying a 12-month waiting period to pregnancy-related expenses, there still remains uncertainty as to how high-risk women navigate the public–private maternal health system, particularly for subsequent pregnancies. In addition to these general market observations, PHI is community-rated in Australia, so insurers cannot set actuarially fair premiums by detailed individual risk characteristics like unregulated classes of insurance, and this may increase the potential of adverse selection (Buchmueller, Reference Buchmueller2008). Conversely, policies designed to encourage low-risk demographic groups to purchase PHI may offset the risk of adverse selection. Given these conflicting possibilities, it is pertinent to understand whether there is evidence of adverse selection during the perinatal period as this has public policy implications and can inform risk management and pricing strategies for private health insurers. Therefore, the objectives of our study are threefold: to investigate the profiles of women by patient status (public versus private); PHI status; and transition status (for transitions between the public and private system for a subsequent pregnancy).

2. Methods

2.1 Data

A nationally representative sample of women was randomly recruited to the Australian Longitudinal Study on Women’s Health (ALSWH) through the Medicare database in 1996 and participants have since been surveyed every three to four years (Dobson et al., Reference Dobson, Hockey, Brown, Byles, Loxton, McLaughlin and Mishra2015). The Centre of Health Record and Linkage used probabilistic data linkage principles to link all available data for women residing in New South Wales (NSW) (the largest state in Australia) in the 1973–1978 cohort with the Perinatal Data Collection (PDC) for birth records and the Admitted Patients Data Collection (APDC) for hospital records. The resultant dataset used in our analysis consisted of 3,400 singleton births (from 1,875 women) over the years 2001–2012. Extensive details of this linked longitudinal data have been published elsewhere (William et al., Reference William, Chojenta, Martin and Loxton2018a) and detailed methods of ALSWH have also been previously published (Brown et al., Reference Brown, Bryson, Byles, Dobson, Lee, Mishra and Schofield1998; Dobson et al., Reference Dobson, Hockey, Brown, Byles, Loxton, McLaughlin and Mishra2015). The PDC is a population-based surveillance system covering all births in NSW public and private hospitals, as well as homebirths, and reporting of all births in NSW to the PDC is a statutory requirement (Centre for Health Record Linkage). The APDC contains all inpatient separations (discharges, transfers and deaths) in NSW (Centre for Health Record Linkage).

A woman was defined as a “public” or “private” patient if all hospitalisations during the perinatal period were public or private respectively. Similarly, for PHI status, a woman was defined as having PHI if she had PHI for hospital treatment for all hospitalisations during the perinatal period. When examining patient and PHI status, we excluded births from women that switched between patient status during the perinatal period (a “mixed” group) and women with missing (or not stated) patient and PHI status so that each group was homogenous (N = 2,955). However, we included all births (N = 3,400) when studying the mixed group (N = 229). For transition status, a woman was defined as having a transition if she moved between the public and private system (or vice versa) for her second birth. We only included women for which at least the first two births were recorded in the data and excluded women with missing or not stated patient status (N = 695) when modelling transitions. We modelled cases of private (N = 397) separately to public (N = 298), where private and public were defined as the patient status of her second birth.

In line with previous studies, our clinical definition of “low-risk” was a non-smoking woman aged 20–34 years without pre-eclampsia or diabetes, giving birth at 37–41 weeks gestation to a foetus weighing greater than 2.5 kg in a cephalic presentation (Read et al., Reference Read, Prendiville, Dawes and Stanley1994; Dahlen et al., Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2012). Obstetric interventions were also based on previous studies and are epidural pain relief, induction, instrumental birth (forceps or vacuum), caesarean section and episiotomy (Dahlen et al., Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2012). The perinatal period was defined as the start of the antenatal period (which was defined using gestation age and date of birth of the baby) to the end of the first year following the birth of the baby and we included all hospitalisations of the women in the dataset over this period (William et al., Reference William, Chojenta, Martin and Loxton2018a).

2.2 Statistical analysis

The main purpose of the statistical analysis was to identify factors of statistical significance for public–private patients. We used the two-phase modelling methodology developed by William et al. (Reference William, Chojenta, Martin and Loxton2018a) to account for the vast number of factors available for testing. The two phases include an exploratory phase using Classification and Regression Trees to initially select factors and a formal parametric modelling phase to assess these factors for statistical significance. In the parametric modelling phase, we used standard logistic regression using births as the unit of analysis.

Initially, over one hundred factors were available from the linked datasets to be included in the multivariate models. The factors were broadly grouped into five categories: health service use, obstetric and reproductive factors, sociodemographic factors, health behaviours and psychosocial and physical health factors. Factors selected for formal parametric testing following the exploratory phase are shown in the Supplementary Material and also include factors that were deemed relevant from previous studies (William et al., Reference William, Chojenta, Martin and Loxton2018a,b). For the transition models, we considered factors from the first and the second perinatal periods. We used a 1% significance level to ensure models were parsimonious.

3. Results

Frequencies of selected maternal and neonatal characteristics by patient status are shown in the Supplementary Material. The results of the logistic regressions for a single perinatal period are shown in Table 1. For the patient status model, PHI status was the major driver of whether a patient elected public or private status, even after controlling for other significant factors. We also found private patients had higher self-rated access to specialist services and were more likely to have obstetric interventions. Unsurprisingly, general practitioner use was more likely for public patients, but specialist use was more likely for private patients. Importantly, health-related factors such as physical and mental health factors, health behaviours and conditions particularly problematic for pregnancy (such as high body mass index, diabetes and hypertension) were not statistically significant. Similarly, age, parity, low-risk and sociodemographic factors were statistically insignificant; however, these factors may be captured within PHI status (and were tested therein).

Table 1. Logistic regression output for single perinatal period

Sociodemographic factors were the most dominant explanatory factors for whether a woman had PHI or not. Specifically, a woman was more likely to have PHI if she was older, partnered, more educated, with higher socioeconomic status and without a healthcare card (that is, a concession card for welfare recipients that entitles them to subsidised healthcare costs). Moreover, health-related factors outlined in the previous model were not statistically significant in this model too. Importantly, women who had PHI were more likely to be in the low-risk category and have interventions. We removed the intervention factor to test whether health-related factors became significant (as they may be highly correlated with interventions); however, they were still statistically insignificant. Those who had PHI were also more likely to have higher self-rated access to medical specialists, more likely to use specialists and less likely to use general practitioners. Finally, higher Apgar scores (at 5 minutes) were more likely for births from women with PHI and this result persisted when modelled on low-risk cases only. In summary, the results validated that there was no statistical evidence of adverse selection of PHI and that sociodemographic factors were the overriding influences for purchasing PHI in Australia.

Next we considered transitions between systems across single and multiple perinatal periods. For mixed patient status within a perinatal period, the only factor of significance besides PHI, was in-vitro fertilisation (IVF), which indicated these patients preferred (or needed) access to both systems during their perinatal period. This is possible within the Australian system because patients are able to elect to use both systems, but these results show that it is uncommon, with only 13% of patients transitioning within a perinatal period and likely for a highly specialist service.

Table 2 shows the results of the logistic regressions for transitions across two perinatal periods. Overall, we observed 10% of women transitioned between systems for their second pregnancy – 8% of public patients transferred to the private system for their second baby and the equivalent figure for the public system was 2%. The transition models also showed that a change in PHI status between births was the most significant predictor of whether there was a transition in patient status. This was unsurprising given earlier results showing the key driver of patient status was PHI. For the private model, a woman was also more likely to transition if she had hypertension in her second pregnancy and suggested this transition occurred due to a new health condition (as hypertension in the previous pregnancy was not significant). This factor relates to general hypertension (as opposed to pregnancy-related hypertension) so the condition could have developed in-between pregnancies. A woman was also more likely to transition to the private system if she had less self-rated access to medical specialists and greater stress about motherhood in her first perinatal period. This may indicate that women who purchased PHI in-between pregnancies did so for greater choice in healthcare providers in their next pregnancy or because of a stressful first motherhood experience. We removed the “change in PHI status” factor to test whether health-related factors became significant; however, they were still statistically insignificant (with the exception of hypertension in the second pregnancy for the private model). This is likely due to sociodemographic (rather than health-related) factors driving this change in status.

Table 2. Logistic regression output for transition * models

*“Transition” identifies whether the patient status of the second birth was different to the patient status of the first birth.

4. Discussion

Our study overwhelmingly showed that the key predictor of private patient status was having PHI across both one and two perinatal periods. The decision to purchase PHI was also largely driven by sociodemographic factors, with women who were older, partnered, more educated and with higher socioeconomic status more likely to have PHI. Increased access to specialists and usage of private services were also identified as significant factors for the private setting. Furthermore, there was limited evidence to suggest that women in the private system had more complex health conditions. In contrast, women with PHI were more likely to be lower-risk and have babies with higher Apgar scores (at 5 minutes) (a measure of neonatal health) but also more likely to have an obstetric intervention.

The models for women who transitioned between systems also identified PHI status (rather than health factors) as the key driver for decision-making. For transitions within a perinatal period, IVF was also identified as significant, suggesting that women who receive IVF are using both public and private services during the perinatal period. For transitions over two perinatal periods, we found that 10% of women transitioned from one system to the other for their second perinatal period, and this was largely driven by a change in PHI status when it occurred. Hypertension was the only health condition identified as statistically significant and this was for women transitioning from public to private. This finding suggested that a new health condition may have prompted women to change systems, but as this applied to a small proportion of women it did not impact significantly on the overall drivers of patient and PHI status. The private transition model also showed that access to medical specialists and stress about motherhood were also significant factors for transitioning.

The overwhelming significance of sociodemographic factors in the private setting showed that financial penalties placed on higher income earners in Australia to purchase PHI likely outweighed the possibility of adverse selection of insurance due to community rating as health-related factors were not statistically significant. These socioeconomic disparities by public–private system for women during childbearing years are consistent with general studies that investigated income disparities by system (Hindle & McAuley, Reference Hindle and McAuley2004; Segal, Reference Segal2004; Walker et al., Reference Walker, Percival, Thurecht and Pearse2007; Palangkaraya et al., Reference Palangkaraya, Yong, Webster and Dawkins2009). While studies on public–private maternal health disparities generally acknowledge socioeconomic disparities (Dahlen et al., Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2014; Adams et al., Reference Adams, Tudehope, Gibbons and Flenady2018), they do not directly address the potential for adverse selection during childbearing years largely due to the more detailed health data that is required to inform this.

The risk profiles of privately insured individuals during childbearing years warrant further consideration. We find women with PHI were lower risk, and this may be partly explained by some high-risk women being transferred to specialist units in public hospitals due to the expertise and services available in these units. Therefore, women who were at higher risk and aware of this prior to pregnancy may be less likely to purchase PHI for maternal healthcare in the first place. Moreover, our results suggest that policies introduced to encourage lower risk demographic groups into the private system have had an influence on the risk profiles observed. The few studies that consider adverse selection under current PHI regulations also find that they have been effective in improving general risk profiles of policyholders, especially through the introduction of the LHC (Buchmueller, Reference Buchmueller2008). Our study showed that these findings persist in the perinatal period, with the exception of a small proportion of women who may transition into the private system from the public system after developing hypertension. This is important from an insurer’s risk management perspective, as the perinatal period is a time period during which PHI claims increase considerably (Australian Prudential Regulatory Authority, 2018) and it provides insight into appropriate risk management strategies to counteract adverse selection. Specifically, pre-existing conditions such as hypertension should be disclosed by individuals for insurance purposes and it is prudent to exclude claims on such conditions for some period of time for new policies (that is, impose a waiting period on pre-existing conditions such as hypertension). Notwithstanding these considerations, given our findings on the lower-risk profile of privately insured individuals overall, we determine that government policies have been effective in addressing adverse selection in PHI in the perinatal period.

Our results also highlighted that increased access to maternal health services and “peace of mind” may be the reasons for individuals to purchase PHI. In particular, we found the evidence that women may switch to the private system to obtain greater access to specialist services and peace of mind for a second pregnancy. However, our findings also showed that these options were largely only available to women of better socioeconomic background who were more able to pay and therefore use private services through the purchase of PHI. These findings agree with other studies that favourably value choice and control over healthcare (Natalier & Willis, Reference Natalier and Willis2008; Harley et al., Reference Harley, Willis, Gabe, Short, Collyer, Natalier and Calnan2011; Willis & Lewis, Reference Willis and Lewis2016).

Our findings agree with numerous previous studies that found the rates of interventions were higher in the private setting (Fisher et al., Reference Fisher, Smith and Astbury1995; Shorten & Shorten, Reference Shorten and Shorten2000; Robson et al., Reference Robson, Laws and Sullivan2009; Dahlen et al., Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2012, Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2014; Einarsdóttir et al., Reference Einarsdóttir, Kemp, Haggar, Moorin, Gunnell, Preen and Holman2012, Reference Einarsdóttir, Haggar, Pereira, Leonard, de Klerk, Stanley and Stock2013b). Dahlen et al. (Reference Dahlen, Tracy, Tracy, Bisits, Brown and Thornton2014) argued that it was clinicians’ behavioural differences that increased private intervention rates, even among low-risk women, which resulted in other adverse maternal and neonatal outcomes, and ultimately increased costs incurred. Conversely, other studies have found that neonatal outcomes were better in the private system (Robson et al., Reference Robson, Laws and Sullivan2009; Adams et al., Reference Adams, Gibbons and Tudehope2017, Reference Adams, Tudehope, Gibbons and Flenady2018; Jang et al., Reference Jang, Flatley, Greer and Kumar2017). In particular, Adams et al. (Reference Adams, Tudehope, Gibbons and Flenady2018) control for a vast number of risk factors and conclude that clinical practices may be partly responsible for lower neonatal mortality rates in the private system. Given our findings show limited evidence of adverse selection in the private system but higher rates of interventions, our findings agree with conclusions that there are disparities in clinical practices by system. We recommend further research in this area to understand these interactions better.

The strengths of this study (in contrast to previous studies) are the extensive number of sociodemographic and health-related factors that we were able to test within a multivariate model framework because of the comprehensive linked cohort data used to determine the extent of adverse selection in maternal healthcare. The longitudinal data also allowed us to analyse women across two perinatal periods to study reasons for transitioning between systems for the first time. On the other hand, the main limitations of the study were the smaller-sized dataset for women in one state only (NSW) and a predominantly low-risk cohort of women. Also, although ALSWH recruited a nationally representative sample, there was an over-representation of women with tertiary education and an under-representation of women from non-English-speaking backgrounds (Dobson et al., Reference Dobson, Hockey, Brown, Byles, Loxton, McLaughlin and Mishra2015). There was also the possibility of attrition bias; however, previous analyses have found that this bias was unlikely to be significant (Powers & Loxton, Reference Powers and Loxton2010).

Finally, we note that recent trends show a slight reduction in the proportion of the population with PHI for hospital treatment and a corresponding reduction in the use of private maternal healthcare services in Australia (Australian Institute of Health and Welfare, 2017a, 2017b, 2018). Although it is too early to determine whether this trend will continue or have a significant impact on the risk profile of patients, the results of our study overwhelmingly show limited evidence for adverse selection and it is unlikely that the small movements observed to date will significantly impact on this finding. Furthermore, there are new reforms to the PHI industry (The Department of Health, 2018b) that aim to make it simpler and more affordable. It will take a number of years to implement these new reforms but recommended initiatives should continue to counteract the effect of adverse selection. These reforms will apply in addition to the regulations that are currently in place. We recommend that these issues are revisited once the new policies are in place.

5. Conclusion

When a mixed public–private maternal health system is within a regulatory structure that incentivises specific groups to purchase PHI, sociodemographic factors overwhelmingly influenced decision-making into each system. While it was uncommon to switch between systems, the main factor in transitioning to the private sector for a subsequent pregnancy was change in PHI status. Previous stress about motherhood, previous self-rated access to specialist services, and hypertension were also found to be statistically significant factors for transitioning systems. As the statistical significance of hypertension related only to the small number of cases that transitioned to the private system and health-related conditions were not statistically significant predictors of overall patient or PHI status, we determine that there was limited evidence of adverse selection. We conclude that targeted government regulations in PHI have effectively reduced adverse selection even during the perinatal period of policyholders.

6. Ethics

The ALSWH has been granted ethics clearance by the Universities of Newcastle and the University of Queensland (Ethics approvals H0760795 and 2004000224). Ethics for the longitudinal study was approved on 26 July 1995. This research also received ethical approval from the Australian National University (Protocol: 2017/106).

Author ORCID

Jananie William, https://orcid.org/0000-0003-1986-985X

Supplementary Material

To view supplementary material for this article, please visit https://doi.org/10.1017/S1748499519000083

Acknowledgements

The research on which this study is based was conducted as part of the ALSWH by the University of Queensland and the University of Newcastle. We are grateful to the Australian Government Department of Health for funding and to the women who provided the survey data. We acknowledge the Australian Institute of Health and Welfare as the integrating authority for these data. We thank the NSW Ministry of Health, the NSW Central Cancer Registry and the Centre for Health Record Linkage.

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Table 1. Logistic regression output for single perinatal period

Figure 1

Table 2. Logistic regression output for transition * models

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