Article Text

Original research
Switch from public to private retail pharmaceutical expenditures: evidence from a time series analysis in Italy
  1. Jacopo Lenzi1,
  2. Maria Michela Gianino2
  1. 1Department of Biomedical and Neuromotor Sciences, Alma Mater Studiorum Università di Bologna, Bologna, Emilia-Romagna, Italy
  2. 2Department of Public Health Sciences and Pediatrics, Università degli Studi di Torino, Torino, Piemonte, Italy
  1. Correspondence to Dr Maria Michela Gianino; mariola.gianino{at}unito.it

Abstract

Objectives To analyse trajectories of retail pharmaceutical expenditures from 2010 to 2019 in Italy to investigate whether there was a switch from public to private expenditure, how the composition of private and public expenditure changed, and whether there are correlations with supply/demand variables. Answering these questions is important to assure pharmaceutical care to all citizens in a public health system where expenditure containment is the issue of pharmaceutical policies.

Design and setting Time-trend analysis was carried out in the Italian National Health System (NHS), between 2010 and 2019. We considered the following: public pharmaceutical expenditure with/without direct distribution of drugs, copayments, household out-of-pocket payments for drugs reimbursable/non-reimbursable by the NHS, and for drugs without prescription requirement. Correlations were tested between expenditure items and relevant statistics (Gini coefficient, resident population demographics, ages and categories of physicians, and current expenditure on health).

Results The switch feared between public and private pharmaceutical expenditures was not found: private expenditure increased (average annual per cent change 1.5%; 95% CI 0.3% to 2.6%), but public spending remained stable (–1.0%; 95% CI –3.0% to 1.1%). Single items of expenditure exhibited significant pattern changes over the study period. A switch from public expenditure without direct distribution of drugs (–3.9%) to expenditure with direct distribution was found (+8.4%). Unexpected increases in household out-of-pocket payments for drugs reimbursable by the NHS (+6.1%) and in copayments (+4.9%) were shown. No notable correlations were found.

Conclusions This study offers insights into Italian experience that can be applied to other contexts and the results provide policy-makers issues to reflect on. The findings suggest that policies of pharmaceutical-expenditure management may have multiple effects and unexpected combined effects over time that should be considered when they are designed, and suggest that health policies must be adopted with a systematic logic and a broad and unified vision.

  • health economics
  • health policy
  • organisation of health services

Data availability statement

Data are available upon reasonable request. The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

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Strengths and limitations of this study

  • This is the first study to analyse possible shifts in retail pharmaceutical expenditure from public to private expenditure and change on the composition of expenditures over the time in a National Health System.

  • All pharmaceutical expenditure items were analysed.

  • The study was conducted using administrative data.

  • Expenditure data were not disaggregated at the regional level.

Introduction

Pharmaceuticals play a vital role in the health system. The challenge for policy-makers, acknowledging that healthcare budgets are limited, is to balance the growing demand for drugs and access to new medicines with the economic resources available.

Pharmaceutical expenditure encompasses hospital pharmaceuticals, including drugs administered or dispensed during an episode of hospital care, and to retail pharmaceuticals that are provided outside of hospital care, such as those dispensed through a pharmacy or bought from a supermarket.

Pharmaceutical expenditures are predominantly made for retail pharmaceuticals. In the European Union (EU), retail pharmaceuticals averaged €381 per person across the 27 member states in 2018, adjusted for differences in purchasing power. The variations in per capita retail pharmaceutical spending across countries are wide, ranging from €236 in Denmark to €615 in Germany (Italy showed a per capita expenditure on retail pharmaceuticals of €434).1 These variations reflect differences in the basket of available medicines, in pharmaceutical prices, in consumption and in the relative role of hospitals in dispensing pharmaceuticals, as well as in the market penetration of generics and in the policies adopted.

In recent years, in countries where governments are the largest third-party payers and private companies sell pharmaceutical products, pharmaceutical policies have been mostly driven by the need to control costs.2 Several countries have taken measures to reduce pharmaceutical spending—such as cutting manufacturer prices and margins for pharmacists and wholesalers, introducing compulsory rebates, delisting some pharmaceuticals (ie, excluding them from reimbursement) and incentivising the use of generics.3

Over the last 20 years, Italy’s pharmaceutical policies have changed along three dimensions:

  1. Measures to reduce pharmaceutical spending through reimbursements, negotiated ex-factory prices and payback mechanisms.

  2. Actions to govern demand through copayments in two forms, as a prescription fee and as the spread on the reference price (i.e., the patient pays the difference between the reference price and the pharmacy price), and through actions regarding prescription behaviour, such as setting prescription quotas.

  3. Introduction of alternative forms of drug distribution.

In Italy, the governance of pharmaceutical expenditure is balanced between two levels: national and regional. Since 2001 the Italian healthcare system has been decentralised and each of the 21 regions or autonomous provinces have had power to legislate within the framework established by the central government and have had responsibility for the management, organisation and delivery of healthcare services. At national level, the main regulatory actor is the Agenzia Italiana del Farmaco (AIFA) that manages: marketing authorisation; prices and reimbursement of authorised drugs that are negotiated by the AIFA and the relevant marketing company; reference pricing for the generic off-patent submarket (i.e., the market for active principles with at least one generic form); pay-back to the regions after exceeding the pharmaceutical spending ceiling. The devolution has increased regional accountability on pharmaceutical spending, as a consequence, the regions have implemented policies of cost containment focusing on co-payment and actions on prescribing behaviour, including prescription quotas. Copayment as prescription fee and as spread on the reference price were first introduced by regional governments in 2002, prescription quotas were first introduced in 2005. Pharmaceutical direct distribution of medicines listed in the Direct Distribution Formulary was another measure implemented.

Previous studies have analysed the effect of a single policy4 5 or the impact of multiple policies on a single variable, such as public expenditure, total expenditure or demand,6 7 and little is known about the effect of pharmaceutical policies on the distribution of expenditures between public and private components.2

In particular, little attention has been given to the analysis of a possible shift from public to private expenditure and the effect on the composition of expenditures after policies have been adopted by guaranteeing the sustainability of public spending.

The goal of this study is to analyse the trajectories of retail pharmaceutical expenditures in Italy by exploring the following questions:

  1. Was there a switch in retail pharmaceutical expenditure from public to private spending?

  2. Did the internal composition of private and public expenditure change?

  3. What correlation can be found between retail pharmaceutical expenditures and relevant supply/demand variables?

Materials and methods

This study used a time-trend analysis of annual secondary data from Italy covering the 10-year period between 2010 and 2019. We obtained official data from the Italian Medicine Agency (AIFA), Organisation for Economic Co-operation and Development (OECD), National Institute of Statistics and Eurostat. The indicators considered here are shown in table 1, which lists the definition and source for each. These indicators were chosen because of data availability and for the following reasons: as demographic factors potentially driving pharmaceutical expenditure, we used the most commonly used variables (sex and age structure of the population); as a link to socioeconomic gradient, we used the Gini index; as behavioural factors driving prescription habits, we opted for type of medical practitioners (generalist vs specialist) and age composition of prescribing physicians; as economic factors, we opted for an international indicator, that is, public versus private expenditures share of gross domestic product.

Table 1

Indicators, definitions and data sources

A time-trend analysis was performed using the average annual per cent change (AAPC) as the summary measure for the rate of change over the period 2010–2019. The AAPC is a method that uses an underlying segmented regression in which a number of significant breakpoints in the time series (if any) are allowed, and is computed as a weighted average of the annual per cent changes estimated over each time segment. In our analysis, the AAPC was estimated by fitting a log-linear segmented regression model, assuming the homoscedasticity of the random errors and allowing two breakpoints over the time series.8

Kendall’s τ coefficient was used to investigate the correlations between the observed pharmaceutical expenditure items and other relevant health statistics over the period 2010–2019, including the ages and categories of practising physicians, current expenditure on health, the Gini coefficient and resident population demographics; values of τ range from –1 (perfect negative association) to +1 (perfect positive association). Kendall’s τ was preferred over Spearman’s ρ because its normal approximation does not require large-sized or moderate-sized datasets to be valid.9 The correlation analysis was performed on first-differenced (detrended) data.

Time-trend analysis was conducted with Joinpoint Regression Program V.4.8.0.1 (April 2020; Statistical Methodology and Applications Branch, Surveillance Research Program, National Cancer Institute), while correlation analysis was conducted with Stata V.15 (StataCorp. 2017. Stata Statistical Software: Release 15. College Station, TX: StataCorp LLC). All tests were two sided and the significance level was set at 5%. Raw data used for the analysis are presented in online supplemental file 1.

Patient and public involvement

Patients and the public were not involved in the design or planning of the study.

Results

Italy’s public pharmaceutical expenditure did not change significantly between 2010 and 2019 (AAPC = –1.0%, 95% CI –3.0% to +1.1%), while private pharmaceutical spending increased significantly (AAPC =+1.5%, 95% CI +0.3% to +2.6%). As shown in figure 1, nearly all single items of expenditure did exhibit significant patterns of change over the study period. More specifically, public pharmaceutical expenditure without the direct distribution of drugs in class A experienced a pronounced slowdown (AAPC = –3.9%, 95% CI –4.5% to –3.4%), and public pharmaceutical expenditure with the direct distribution of drugs in class A exhibited a significant increase (AAPC =+8.4%, 95% CI +3.6% to +13.3%) over 10 years. The increase in private pharmaceutical expenditure was mainly driven by an increase in expenditure on drugs in class A (AAPC =+6.1%, 95% CI +1.7% to +10.7%) and in copayments (AAPC =+4.9%, 95% CI +3.6% to +6.0%).

Figure 1

Public (red) and private (blue) pharmaceutical spending in Italy between 2010 and 2019 (millions of euros). The average annual per cent change (AAPC) of each item is reported on the right side of the chart; * indicates that the AAPC is significantly different from zero at the 5% level. Notes: the AAPC is a summary measure of the trend over a prespecified fixed interval. It is obtained from an underlying segmented regression in which a number of significant breakpoints in the times series (if any) are allowed, calculating a weighted average of the annual per cent changes estimated over each time segment. Data source: AIFA: Italian Medicine Agency; NHS, National Health Service.

Table 2 shows the results of the correlation analysis, which evaluates the relationship between supply/demand variables and pharmaceutical expenditures. The only slightly significant results relate to the positive correlation between income inequality and out-of-pocket expenses for drugs without prescription requirement (over/behind the counter) (τ=0.62, p value=0.046).

Table 2

Kendall’s τ correlation coefficients (p values) for annual detrended pharmaceutical expenditure items (millions of euros) versus the number of medical practitioners aged 55–64 and ≥65 years, number of specialists, current expenditure on health (% of GDP), Gini coefficient (%), and resident population demographics (female, 65–79 and ≥80 years); Italy, 2010 to 2019 (10 years)

Discussion

The switch feared between public and private pharmaceutical expenditures was not found: between 2010 and 2019, Italy’s private pharmaceutical expenditure increased, but public spending remained stable.

Composition of private pharmaceutical expenditure

The composition of private expenditure seems to have changed due to significant growth in copayments. This result may be explained by the combined effect of the different trends in the two types of pharmaceutical expenditure sharing the differential with respect to the reference price and fixed rate tickets. Since 2001 (law 405/2001),10 the regions have been given the right to apply a prescription fee with the dual aim of reducing government expenditure through a payment shift from third-party payers to patients and of promoting the rational use of drugs. In 2014, drugs were subjected to prescription fees in 16 out of 21 regions; in 2019, drugs were subjected to prescription fees in 18 out of 21 regions. This policy seems to have led to a reduction in the weight of fixed rate tickets, which was estimated to have fallen by –17.7% between 2013 and 2019,11 and seems to confirm the results of previous studies according to which copayment policies have been shown to decrease purchases of pharmaceuticals in countries with diverse health systems.12 13

This decrease is hard to interpret because, as suggested by some authors, an explanation could be sought in a more responsible use of medicines.12 14 A different explanation, as suggested by other authors, could be sought in decreased patient access to drugs and reduced drug cart, leading to a negative impact on long-term health outcomes.15 16

The different composition of private expenditure may also be attributable to the differential share of brand-name drugs in total drug purchases, as such drugs are preferred to generic equivalents. Although Italy has implemented actions to favour generic consumption, such as the introduction of mandatory generic substitution by pharmacists in 2005 and mandatory generic prescription by physicians in 2012 (Law 135/2012),17 the low diffusion of equivalent drugs in our country persists. This finding is documented in numerous international comparisons: although between 2005 and 2017 it went from 7% to 25% in volume, the market share of generic drugs in Italy remains considerably below the EU average, and in 2019, out of 13 OECD countries, Italy ranked last in terms of the value (9.1%) and second-to-last in terms of the volume (27.7%) of equivalent drugs purchased. This result can be explained by the combined effect of (1) a reduction in the price of generic drugs that occurred in 2011 and (2) the remuneration of pharmacists calculated on the basis of a fixed percentage of the price of the products, an aspect that constitutes a disincentive to propose generic drugs to customers (less expensive). Indeed, if they are paid by fixed margins of the retail price, the pharmacists have an incentive to sell the highest priced pharmaceuticals. In addition, according to the literature, the roots of this demand for brand-name medicines rather than generics could be found in consumer behaviours affected by negative perceptions of generic medicines18 and subsequent negative attitudes towards generic substitution.19–23 A strong lack of confidence in the quality of ‘copycat’ medicines attributed to the decreased effectiveness of generic medicines18 24 may explain the willingness to pay slightly more for an original drug than for a generic alternative. This suggestion is supported by a previous study showing an incoherent generic medicine policy in Italy, with demand-side policies for physicians and pharmacists but not for patients,25 who have not received any information or education about generic drugs.

Composition of private and public pharmaceutical expenditure for drugs in class A

A surprising and unexpected result of this study is the increase in expenses for medicines that are reimbursable (class A) but were bought privately; even more surprising is that both the expenditure for the direct distribution of drugs in class A and the expenditure for class A drugs borne by the citizens grew as if there were a complementarity between the two items. A previous study26 showed a positive correlation between the volumes (and expenditure) of prescription-only drugs reimbursed by the National Health System (NHS; class A) and non-prescription drugs for several therapeutic classes, but to our knowledge, no study has explained this correlation. The explanation for this phenomenon does not seem to be rooted in social and economic inequality or in ageing or gender, as suggested by previous studies.27 28 Since no significant correlation was found between the Gini index or the elderly resident population and the level of private pharmaceutical expenditure, it cannot be inferred that these variables lead to a certain expenditure level. A possible explanation could be the presence of a barrier in access to GPs, implying that patients do not go to the GP to be prescribed drugs, but due to the prescription of a specialist, they go directly to community pharmacies.

Composition of public pharmaceutical expenditure

The results of this study also showed a change in the trend in public expenditure and in its composition, with greater growth in the direct distribution of drugs and a significant reduction in expenditure without the direct distribution of drugs reimbursed by the NHS. The switch seems to be conditioned by the fact that all regions have activated direct pharmaceuticals through two different channels: distribution of reimbursable medicines to patients by hospitals and other healthcare structures; distribution of medicines directly bought by the NHS by community pharmacies (distribution on behalf of the NHS) through agreements stipulated with wholesalers and pharmacy associations.

In both channels, very aggressive procurement policies have been adopted in recent years through the establishment of hospital networks (even at the regional level) to increase their bargaining power, and require companies to offer further discounts.29 Faced with such policies, one would expect a reduction in the value of expenditure. Instead, this change suggests that direct price controls may be less effective in controlling spending, as savings are offset by a sharp increase in volume.30 Indeed, Tele and Groot found that most cost-containment policies consist of supply-side measures, as such measures have proven to be more effective than demand-side measures, and that price control policies are most effective in controlling expenditure when accompanied by complementary volume control measures.31

Study limitations

First, we use administrative data to analyse the composition of private and public expenditures. This database often does not record all data, and no information is available on volumes, types or mixes of drugs, as we only observed expenditures for drugs that were prescribed and sold. Consequently, we did not take into account the quantities of drugs used, an increase which may be explained by a range of factors: population ageing; the rise in the prevalence of chronic diseases such as cancer, cardiovascular disease and mental illnesses; the possibility that pharmaceutical companies may increase the prices of other drugs as a result of generic substitution; or the introduction of new and generally more expensive drugs—including new formulations of existing medicines—which pushes spending up.3 Second, we used aggregate data at the country level and, due to data unavailability, had no possibility to explore the impact of regional differences. Since 2001, the Italian healthcare system has been decentralised, and the regions have had the power to legislate and the responsibility to manage and organise the delivery of healthcare services. Many pharmaceutical policies are managed at the regional level, including the direct distribution of drugs and copayment measures, with huge differences across regions. These differences may explain the effects of pharmaceutical policies on the expenditure trend. A 2017 study showed that private spending grew at a higher rate in northern regions, which have introduced tickets since 2002/2003, than in southern regions, which adopted this policy later.32 Lastly, a lack of power due the short time period covered by our study may have been responsible for not finding significant correlations between supply/demand and pharmaceutical expenditure.

Conclusion

Despite some considerable limitations, this study contributes to the literature and fills a gap represented by the analysis of the trajectories of retail pharmaceutical expenditures and of the change in the composition of expenditures over time. Results of this study focus on the experience of Italy, but readers can take certain aspects of Italian experience and apply them to other contexts and the results offer policy-makers issues to reflect on. (1) Pharmaceutical expenditure has increased over time, and although there has been no switch from public to private, private expenditure has grown more than public expenditure. These results suggest that pharmaceutical policies can have unexpected combined effects over time and in contrast with the spirit of the public health system’s call for affordable and quality healthcare for all and a reduction in the direct financial burden on the population accessing care. (2) There has been a switch from expenditure without direct distribution of drugs reimbursed by the NHS to expenditure with direct distribution. The second grew more than twice as much as the first decreased. These results suggest that ‘policies have multiple effects that should be considered when they are designed’.2 For example, direct distribution may be intended to contain prices, but it may increase volumes or cause the mix of drugs, compensating for the expected effect. (3) There has been an increase in copayments (due to the preference for brand-name drugs over equivalents). The policies to be adopted must consider not only the payer’s perspective but also the perspectives of all other stakeholders (patients, prescribers, pharmacists, etc) and must provide for their direct involvement if one wants the effect expected from each policy. (4) There has been increasing expenditure on drugs reimbursable by the NHS but paid for by citizens. This could be an alarm for a public healthcare system that should be able to guarantee healthcare services, and suggests that health policies must be adopted with a systematic logic and a broad and unified vision,33 considering the fact that policies in different fields can interact with each other with unexpected effects.

Data availability statement

Data are available upon reasonable request. The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Ethics statements

Patient consent for publication

Ethics approval

This study does not involve human participants.

References

Supplementary materials

  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

Footnotes

  • Contributors MMG formulated the research goals; defined the design of the methodology; wrote the article. JL collected the data and managed the database, used statistical techniques to analyse the study data. All authors have read and approved the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.