Abstract
Background
Although tuberculosis (TB) patients often incur high costs to access TB-related services, it was unclear beforehand whether the implementation of universal health coverage (UHC) in Indonesia in 2014 would reduce direct costs and change the pattern of care-seeking behaviour. After its introduction, we therefore assessed TB patients’ care-seeking behaviour and the costs they incurred for diagnosis, and the determinants of both.
Methods
In this cross sectional study, we interviewed adult TB patients in urban, suburban, and rural districts of Indonesia in July–September 2016. We selected consecutively patients who had been treated for TB in primary health centers for at least 1 month until we reached at least 90 patients in each district. After establishing which direct and indirect costs they had incurred during the pre-diagnostic phase, we calculated the total costs (in US Dollars). To identify the determinants of these costs, we applied a general linear mixed model to adjust for our cluster-sampling design.
Results
Ninety-three patients of the 282 included in our analysis (33%) first sought care at a private clinic. The preference for such clinics was higher among those living in the rural district (aOR 1.88, 95% CI 0.85–4.15, P = 0.119) and among those with a low educational level (aOR 1.69, 95% CI 0.92–3.10, P = 0.090). Visiting a private clinic as the first contact also led to more visits (β 0.90, 95% CI 0.57–1.24, P < 0.001) and higher costs than first visiting a Primary Health Centre, both in terms of direct costs (β = 16.87, 95%CI 10.54–23.20, P < 0.001) and total costs (β = 18.41, 95%CI 10.35–26.47, P < 0.001).
Conclusion
Despite UHC, high costs of TB seeking care remain, with direct medical costs contributing most to the total costs. First seeking care from private providers tends to lead to more pre-diagnostic visits and higher costs. To reduce diagnostic delays and minimize patients’ costs, it is essential to strengthen the public-private mix and reduce the fragmented system between the national health insurance scheme and the National TB Programme.
Keywords: Tuberculosis, Costs, Care-seeking behaviour, Universal health coverage, Indonesia
Background
Studies in Asian countries suggest that the private healthcare sector has the potential to play an important role in national and global tuberculosis (TB) control [1–4]. Many studies have shown that patients initially visit private providers to relieve them from TB-related symptoms [5]. In Indonesia, many patients also prefer first to seek care from private providers [4]. However, private providers often fail to comply with TB practice guidelines, including those for the screening and diagnosis of TB cases [4, 6]. In the pre-diagnostic phase, failure to comply with TB practice guidelines may lead to missed TB cases. Patients who continue to have TB related symptoms then have many healthcare visits [7], leading to diagnostic delays and high costs during seeking care [8, 9]. This eventually worsens disease prognosis at the individual level, increases costs in the household level, and spreads TB in the community [8, 10].
In 2014, Indonesia started implementing a universal health coverage (UHC) scheme, also called the Indonesian National Health Insurance scheme (Jaminan Kesehatan Nasional, JKN), to ensure people’s access to healthcare. This insurance scheme is managed by the Social Security Agency for Health (Badan Penyelenggara Jaminan Sosial Kesehatan, BPJS-K) and covers all essential care services, including TB diagnostic tests through healthcare providers that are linked to the BPJS-K [9, 11]. In the first 4 years after the JKN was implemented, the number of private providers linked to the BPJS-K – clinics and solo practices alike – increased substantially, from 6369 private providers to 11,507 [12].
However, BPJS-K is not directly linked to the network of the Indonesian National Tuberculosis Program (NTP), which are national level government boards that are responsible for TB control. Private providers that are linked to the BPJS-K are therefore also not necessarily linked to the NTP. Responding to this problem, the NTP launched a guideline of TB care to coordinate the care with the BPJS-K [13]. Although there has been no direct linkage between the NTP and BPJS-K, the private providers that are linked with BPJS-K can conduct the TB tests in their laboratories, if available, or can refer suspected TB patients for diagnostic tests to a BPJS-K-linked facility [13]. All consultation and diagnostic test fees are covered by the BPJS-K. If the suspected patient has received the final TB diagnosis, the private providers can refer the patient to the NTP-linked facilities to receive free TB treatment. As most TB patients seek initial care with a private provider [6], this coordinated scheme between BPJS-K and the NTP is assumed to reduce patient’s direct costs during the pre-diagnostic phase.
Nevertheless, there is no evidence available on the costs incurred during the pre-diagnostic phase of TB and TB patients’ care seeking behaviour since the implementation of UHC in Indonesia. It is therefore unclear to which extent UHC has saved patients from high costs during this phase. The aims of this study are to assess the costs incurred before diagnosis by patients seeking care for TB after the implementation of UHC in Indonesia, and to assess care-seeking behaviour of TB patients in this period on the basis of the first contact facility and the number of healthcare visits.
Methods
Study design and setting
To assess patients’ TB care-seeking behaviour and the costs they incurred during the pre-diagnostic phase, we conducted a cross-sectional study that was a part of a larger study on measuring catastrophic costs in Indonesia [9]. In this study, we interviewed patients who had undergone TB treatment in PHCs (i.e. public facilities for primary-level care). We selected three districts in Java, the most populous island of Indonesia, purposively to represent urban (Jakarta), suburban (Depok), and rural (Tasikmalaya) areas of Indonesia.
Study population
We included all subjects who met the inclusion criteria of our main study, which were adult patients who had received TB treatment in a PHC for at least 1 month. We excluded extra-pulmonary cases, as these are diagnosed using different methods that may result in bias on pre-diagnostic costs.
Sampling method
The sample size and sampling methods in this study followed that of our larger study, which assumed an incidence of catastrophic costs due to TB of 20–30% [9]. We used a sample size formula for a cross sectional study (Zα2.p.q/d2) with assumptions of a power of 0.90 and an error of 0.05. With a ratio of TB patients of 1:1:1 in each district, we required 90 patients per district. In each district, we included all the PHCs that were linked to the Indonesian NTP in our sampling framework, and then randomly selected five PHCs per district. We chose only PHCs since most of TB patients were treated in PHCs. In each PHC, we selected consecutively adult TB patients until we reached at least 90 patients per district. If the sample size was not reached, we randomly selected additional PHCs until we obtained at least 90 patients per district. In total, 19 PHCs were included in our study.
Data collection
All patients were interviewed by four medical students and six public health graduates we had recruited and trained for the purpose. As a part of our main study on measuring catastrophic costs, the interview was conducted during the TB treatment phase – 48% of patient in their intensive phase and 52% of patients in their continuous phase [9]. To interview the patients and/or the drug observer who accompanied each patient as a direct observation of treatment (DOT) supporter, these interviewers used the adapted and validated Bahasa Indonesia version of the Tool to Estimate Patient Costs [14].
Retrospectively, each respondent listed each healthcare facility he or she had visited between developing TB-related symptoms (e.g., chronic cough, bloody cough, weight loss, or night sweating) and the establishment of their TB diagnosis [14]. We also calculated the number of healthcare visits and costs incurred during the pre-diagnostic phase, and then assessed the determinants of the number of visits and costs.
Care seeking behavior
First, to assess patients’ care-seeking behaviour, we established the nature of their first contact facility, i.e., a primary health centre (PHC); a private clinic (whether a solo practice or part of a multiple practice); a public hospital; a private hospital; or ‘other’, such as a pharmacy, a practitioner of alternative medicine, or a mantri (i.e., a registered nurse practicing as an unauthorized physician). We then assessed whether the first contact facility was associated with the district (urban/suburban/rural), household income level (poor/non-poor household), educational level (low/middle-high), health insurance status (being covered/not being covered by the BPJS-K scheme), and formal employment (yes/no).
Number of visits
Second, we calculated the number of healthcare visits made during the pre-diagnostic phase. To assess the determinants of the number of visits, we also included first contact as an independent variable, together with the other independent variables.
Costs of care seeking
Third, we asked patients the details of all the types of cost they had incurred in each facility visited during the pre-diagnostic phase, i.e., direct medical costs, direct non-medical costs, and indirect costs related to seeking care for their TB-related symptoms. The definitions of cost items used in this study conformed with the WHO handbook on TB costs survey [15]. The direct medical costs included all out-of-pocket (OOP) payments to the healthcare facilities for medical fees, such as administrative charges and the cost of drugs, laboratory analyses, or X-ray examinations. The direct non-medical costs included the cost of food and travel for patients and/or their guardian during their visits to healthcare facilities. The indirect costs consisted of loss of income incurred by the patients and their guardians on their visits to healthcare facilities. The total costs were the sum of direct medical costs, direct non-medical costs, and indirect costs. All costs were provided in Indonesian Rupiahs (IDR) and then converted to US dollars using the World Bank’s average exchange rate for 2015 (1 USD = 13,389.41 IDR). We then assessed whether the total costs, direct costs, and indirect costs were associated with the first contact, district, household income level, educational level, health insurance status, and formal employment.
Data management and analysis
Data were double-entered into Microsoft Excel 2010 and EpiInfo version 7 (CDC, Atlanta) and then exported to IBM SPSS 21 for data analysis. Number of visits and costs data were displayed as means and their 95% confidence intervals (CIs) while categorical variables as numbers and proportions (%). To examine the determinants of the patients’ first contact facility, the number of visits, and their costs during the pre-diagnostic phase, we applied the generalized linear mixed models (GLMMs) with random effects to adjust for our cluster sampling design (19 PHCs), since we selected the PHCs randomly. We assessed the goodness of fit for models by examining the Akaike corrected and the Bayesian information criterion provided by SPSS. To analyse the determinants of the first health-service contact, we estimated crude odds ratios (cORs), adjusted odds ratios (aORs), and their 95% CIs with a target distribution of multinomial regression. To analyse the determinants of number of visits and costs incurred by patients and their family, we established crude and adjusted GLMM regression coefficients (β) and their 95% CIs with a target distribution of linear regression.
Ethical issues
Before the interview, we provided all respondents with a written and oral explanation of the study. Only those who had signed an informed consent form were interviewed. Before the study, we received ethical clearance from the Ethical Committee at the Faculty of Medicine of Universitas Indonesia–Cipto Mangunkusumo Hospital, Jakarta, Indonesia (No. 416/UN2.F1/ETIK/VI/2016).
Results
We included the interviews of 282 patients. Whereas a PHC had been the first point of diagnostic care-seeking for 45% of them, 33% had first sought care at a private clinic, 11% at a public hospital, 7% at a private hospital, and 4% at a pharmacy, practitioner of alternative medicine, or other healthcare provider. (Table 1) A majority of patients (58%) had been diagnosed at a PHC. The remainder had been diagnosed at a private clinic (15%), public hospital (18%), or private hospital (9%) before they were referred to PHCs for TB treatment.
Table 1.
Healthcare service | First point of care | Place of diagnosis | ||
---|---|---|---|---|
N | % | n | % | |
Primary health centre | 127 | 45 | 164 | 58 |
Private clinic | 93 | 33 | 43 | 15 |
Public hospital | 32 | 11 | 50 | 18 |
Private hospital | 20 | 7 | 25 | 9 |
Other health providera | 10 | 4 | 0 | 0 |
aPharmacy, practitioner of alternative medicine, mantri, or other health provider
Figure 1 shows the most common care-seeking patterns identified in this study. Seventeen percent of patients had been diagnosed during their first visit at PHC. This was higher than the percentage of patients who had been diagnosed during their first visit to any of the other healthcare settings. All patients who had first sought care at a pharmacy, practitioner of alternative medicine or other healthcare provider had moved to another provider – usually a private clinic – for their second visit.
Table 2 shows that in the urban and suburban districts, more patients initially sought care at a PHC than at another healthcare facility. In contrast, among patients with low education level, the proportion of those who initially sought care at a private clinic was higher than at another healthcare facility.
Table 2.
Characteristics | Primary health centre N (%) |
Private clinic N (%) |
Public hospital N (%) |
Private hospital N (%) |
Other health providera N (%) |
Total |
---|---|---|---|---|---|---|
Number of patients | 127 (45) | 93 (33) | 32 (11) | 20 (7) | 10 (4) | 282 (100) |
Districts | ||||||
Urban | 51 (54) | 26 (27) | 11 (12) | 4 (4) | 3 (3) | 95 (100) |
Suburban | 40 (44) | 25 (28) | 10 (11) | 13 (14) | 2 (2) | 90 (100) |
Rural | 36 (37) | 42 (43) | 11 (11) | 3 (3) | 5 (5) | 97 (100) |
Household income levelb | ||||||
Non-Poor | 51 (48) | 30 (28) | 12 (11) | 13 (12) | 1 (1) | 107 (100) |
Poor | 76 (43) | 63 (36) | 20 (11) | 7 (4) | 9 (5) | 175 (100) |
Education levelc | ||||||
Middle-High | 89 (49) | 50 (27) | 22 (12) | 15 (8) | 7 (4) | 183 (100) |
Low | 38 (38) | 43 (43) | 10 (10) | 5 (5) | 3 (3) | 99 (100) |
National health insurance | ||||||
Not covered | 48 (44) | 41 (37) | 8 (7) | 7 (6) | 6 (5) | 106 (100) |
Covered | 79 (46) | 52 (30) | 24 (14) | 13 (8) | 4 (2) | 176 (100) |
Workers in informal sectors | ||||||
No | 41 (51) | 25 (31) | 7 (9) | 5 (6) | 3 (4) | 81 (100) |
Yes | 86 (43) | 68 (34) | 25 (12) | 15 (7) | 7 (3) | 201 (100) |
a Pharmacy, alternative medicine, mantri, and other health providers
b household earning below 1.9 USD per capita per day was classified as a poor household
c a patient who did not graduate from elementary school was classified as having low education level
Table 3 shows that more patients in the rural district preferred to seek care first at a private clinic (cOR 2.27, 95% CI 1.14–4.53, P = 0.020). Seeking inital care at a private provider rather than a PHC was also greater among patients with a low educational level than among those with a middle to high educational level (cOR 1.93, 95% CI 1.09–3.41, P = 0.024). Despite the borderline statistical significance of the result, multivariable analysis showed that the odds of seeking care at a private clinic rather than at a PHC was higher in the rural district (aOR 1.87, 95% CI 0.85–4.15, P = 0.119) and in patients with low education level (aOR 1.69, 95% CI 0.51–1.65, P = 0.090). There were no statistically significant differences regarding first contact preferences for the following: between patients with insurance and without insurance; between patients living in a poor household and a non-poor household; and between patients with and without formal work.
Table 3.
Characteristics | Private clinic N (%) |
PHCa N (%) |
P | cOR (95% CI) | P | aOR (95% CI) |
---|---|---|---|---|---|---|
Districts | ||||||
Urbana | 26 (27) | 51 (54) | 1 | 1 | ||
Suburban | 25 (28) | 40 (44) | 0.557 | 1.24 (0.60–2.55) | 0.462 | 1.32 (0.63–2.76) |
Rural | 42 (43) | 36 (37) | 0.020 | 2.27 (1.14–4.53) | 0.119 | 1.88 (0.85–4.15) |
Household income level‡ | ||||||
Poor | 63 (36) | 76 (43) | 0.355 | 1.32 (0.74–2.35) | 0.824 | 1.07 (0.57–2.01) |
Non-Poora | 30 (28) | 51 (48) | 1 | 1 | ||
Education level± | ||||||
Low | 43 (43) | 38 (38) | 0.024 | 1.93 (1.09–3.41) | 0.090 | 1.69 (0.92–3.10) |
Middle to higha | 50 (27) | 89 (49) | 1 | 1 | ||
National health insurance | ||||||
Covered | 52 (30) | 79 (46) | 0.468 | 0.81 (0.46–1.43) | 0.768 | 0.92 (0.51–1.65) |
Not covereda | 41 (37) | 48 (44) | 1 | 1 | ||
Workers in informal sectors | ||||||
Yes | 68 (34) | 86 (43) | 0.364 | 1.32 (0.72–2.41) | 0.284 | 1.40 (1.76–2.58) |
Noa | 25 (31) | 41 (51) | 1 | 1 |
aReference category; ‡ household earning below 1.9 USD per capita per day was classified as a poor household; ± a patient who did not graduate from elementary school was classified as having low education level
The average number of visits during the pre-diagnostic phase was 2.56 (95% CI 2.41–2.71). Patients who first sought care at private clinics and other health care providers had more visits until their diagnosis was confirmed than patients who first visited a PHC (aβ 0.90, 95% CI 0.57–1.24, P < 0.001 for private clinics and aβ 1.77, 95% CI 0.97–2.57, P < 0.001 for other health care providers). (Table 4) There were no statistically significant differences in the number of visits regarding the following determinants: district, household income level, educational level, having insurance, and employment status.
Table 4.
Variables | No of visits mean (95% CI) |
cβ (95% CI) | P | aβ (95% CI) | P |
---|---|---|---|---|---|
Total number of visits | 2.56 (2.41–2.71) | ||||
First contact facility | |||||
Primary Health Centre | 2.18 (1.96–2.41) | Ref | Ref | ||
Private clinic | 3.06 (2.83–3.30) | 0.89 (0.57–1.22) | < 0.001 | 0.90 (0.57–1.24) | < 0.001 |
Public hospital | 2.13 (1.77–2.48) | − 0.07 (− 0.55–0.41) | 0.766 | − 0.08 (− 0.56–0.41) | 0.750 |
Private hospital | 2.65 (2.06–3.24) | 0.44 (− 0.14–1.02) | 0.140 | 0.39 (− 0.20–0.99) | 0.194 |
Other health provider | 3.9 (2.66–5.14) | 1.70 (0.91–2.49) | < 0.001 | 1.77 (0.97–2.57) | < 0.001 |
District | |||||
Urban | 2.49 (2.18–2.63) | Ref | Ref | ||
Suburban | 2.63 (2.37–2.90) | 0.21 (−0.29–0.70) | 0.406 | 0.17 (− 0.31–0.66) | 0.484 |
Rural | 2.56 (2.34–2.78) | 0.11 (−0.39–0.62) | 0.667 | −0.05 (− 0.57–0.48) | 0.861 |
Household income levela | |||||
Poor | 2.58 (2.38–2.77) | 0.07 (−0.25–0.40) | 0.656 | 0.02 (−0.34–0.31) | 0.927 |
Non-poor | 2.53 (2.29–2.78) | Ref | Ref | ||
Education levelb | |||||
Low | 2.66 (2.39–2.92) | 0.16 (−0.17–0.49) | 0.336 | 0.14 (−0.22–0.43) | 0.526 |
Middle-high | 2.51 (2.32–2.70) | Ref | Ref | ||
National health coverage | |||||
Covered | 2.58 (2.37–2.79) | 0.07 (−0.25–0.39) | 0.673 | 0.18 (−0.13–0.49) | 0.259 |
Not covered | 2.53 (2.32–2.74) | Ref | Ref | ||
Workers in informal sectors | |||||
Yes | 2.55 (2.37–2.72) | −0.07 (−0.41–0.27) | 0.692 | −0.12 (− 0.44–0.21) | 0.480 |
No | 2.59 (2.29–2.90) | Ref | Ref |
β is the GLMM coefficient of the expected change in the number of visits compared to the reference category; cβ crude coefficient β; aβ adjusted coefficient β; CI confidence interval; Ref reference; P value of significance; a household earning below 1.9 USD per capita per day was classified as a poor household; b a patient who did not graduate from elementary school was classified as having low education level
The average total cost incurred during the pre-diagnostic phase was USD 22 (95% CI 18–26). It consisted mainly of direct costs (USD 16, 95% CI 13–19). (Table 5) Visiting a private clinic as the first point of contact led to statistically significantly higher costs than visiting a PHC as the first contact, both in terms of direct costs (β 16.87, CI 95% 0.54–23.20, P < 0.001) and of total costs (β 18.41, CI 95% 10.35–26.47, P < 0.001). Patients who visited a private hospital as the first contact also incurred statistically significantly higher direct costs (β 28.38, CI 95% 17.18–39.58, P < 0.001) and total costs (β 24.96, CI 95% 10.64–39.28, P = 0.001) than those visiting a PHC as the first contact. The direct medical costs incurred by patients who first sought care at private clinics (USD 21; 95% CI USD 15–28) and private hospitals (USD 32; 95% CI USD 17–48) were significantly higher than those who first sought care at PHCs (USD 5; 95% CI USD 3–7), while travel costs between private providers and PHCs did not differ significantly (See Additional file 1). Despite involving a higher number of visits, first visiting a pharmacy, practitioner of alternative medicine or other health provider did not lead to significantly higher costs than those incurred by patients who first sought care at a PHC. Between districts, insurance coverage, household income level, and education level, the differences in the total costs, direct costs, and indirect costs incurred were not statistically significant. Indirect costs during the pre-diagnostic phase were associated with employment status. In addition, patients who were formally employed had higher indirect costs than patients who did not have a job or were not formally employed (β 3.92, CI 95% 0.88–6.96, P = 0.012). No other variables determined the indirect costs.
Table 5.
Variables | Total costs | Direct costs | Indirect costs | ||||||
---|---|---|---|---|---|---|---|---|---|
Mean (95% CI) |
β (95% CI) | P | Mean (95% CI) |
β (95% CI) | P | Mean (95% CI) |
β (95% CI) | P | |
Costs | 22 (18–26) | 16 (13–19) | 6 (4–7) | ||||||
First contact facility | |||||||||
Primary Health Centre | 14 (10–17) | Ref | 8 (6–10) | Ref | 6 (4–8) | Ref | |||
Private clinic | 32 (23–41) | 18.41 (10.35–26.47) | < 0.001 | 25 (18–32) | 16.87 (10.54–23.20) | < 0.001 | 7 (4–10) | 1.75 (−1.44–4.95) | 0.280 |
Public hospital | 18 (9–27) | 5.30 (−6.46–17.06) | 0.376 | 13 (7–18) | 4.98 (−4.22–14.18) | 0.288 | 6 (1–10) | 0.19 (− 4.48–4.85) | 0.937 |
Private hospital | 37 (22–52) | 24.96 (10.64–39.28) | 0.001 | 36 (20–51) | 28.38 (17.18–39.58) | < 0.001 | 1 (0–3) | −3.50 (−9.19–2.18) | 0.226 |
Other health provider | 18 (7–29) | 5.38 (−14.02–24.78) | 0.586 | 14 (5–24) | 6.83 (−8.40–22.06) | 0.378 | 4 (−1–8) | −1.32 (− 8.99–6.36) | 0.736 |
District | |||||||||
Urban | 23 (14–31) | Ref | 16 (9–22) | Ref | 7 (4–10) | Ref | |||
Suburban | 20 (15–25) | −1.18 (−12.55–10.20) | 0.839 | 16 (11–21) | 1.81 (−6.89–10.50) | 0.683 | 3 (2–5) | −3.23 (− 7.94–1.48) | 0.178 |
Rural | 23 (19–28) | 1.80 (−9.79–13.39) | 0.760 | 17 (13–20) | 1.57 (− 7.22–10.36) | 0.725 | 7 (5–9) | 0.23 (− 4.62–5.08) | 0.926 |
Household income level‡ | |||||||||
Poor | 22 (17–28) | 1.93 (−5.77–9.63) | 0.622 | 17 (13–21) | 1.59 (−4.57–7.74) | 0.612 | 6 (4–7) | 0.16 (−2.80–3.11) | 0.918 |
Non-poor | 21 (16–26) | Ref | 15 (11–19) | Ref | 6 (3–8) | Ref | |||
Education level± | |||||||||
Low | 22 (18–27) | 0.42 (−7.40–8.24) | 0.916 | 17 (13–20) | 0.61 (−5.638–6.86) | 0.848 | 6 (4–8) | −0.22 (−3.25–2.75) | 0.869 |
Middle-high | 22 (16–27) | Ref | 16 (12–20) | Ref | 6 (4–8) | Ref | |||
National health insurance | |||||||||
Covered | 20 (16–23) | −5.50 (−13.17–2.17) | 0.159 | 14 (12–17) | −4.785 (− 10.89–1.32) | 0.124 | 5 (4–7) | −0.64 (−3.59–2.32) | 0.672 |
Not covered | 26 (18–34) | Ref | 19 (13–26) | Ref | 7 (4–9) | Ref | |||
Workers in informal sectors | |||||||||
Yes | 23 (18–28) | 3.26 (−4.82–11.34) | 0.428 | 16 (12–20) | −0.52 (−7.04–6.00) | 0.876 | 7 (5–9) | 3.92 (0.88–6.96) | 0.012 |
No | 19 (15–24) | Ref | 16 (12–20) | Ref | 3 (2–4) | Ref |
Direct costs include those incurred by patients and/or their guardians during the pre-diagnostic phase for consultation, administrative fees, diagnostic tests (sputum and/or X-ray examination), food, and travel. Indirect costs include their income losses due to visits to healthcare facilities during the pre-diagnostic phase. Total costs are the sum of direct and indirect costs. β is the GLMM coefficient of the expected change in the number of visits compared to the reference category; CI confidence interval; Ref reference; P value of significance; ‡ Household earning below 1.9 USD per capita per day was classified as a poor household. ± A patient who did not graduate from elementary school was classified as having low education level
Discussion
Our results show that patients still incur high costs while seeking TB care. Direct medical costs contributed most to the total costs of TB care seeking, despite the implementation of UHC in Indonesia. Most patients who were treated for TB in a PHC had started their care-seeking in private sector. The number of those who first sought care at a private clinic first was significantly greater among patients who lived in the rural district and among those with a lower educational level. Before being diagnosed with TB, patients who had first sought care at such clinics made more healthcare visits and had higher costs than those whose first point of contact was a PHC.
Rural patients’ preference for starting to seek care at a private clinic may have been affected by the greater distance they had to travel to a PHC. The number of PHCs in these areas is limited, the cost of transport to them is higher, and the waiting times can be long [16]. This encourages patients to visit any private healthcare provider – whether clinic, solo practice or other – that is closer to their house.
However, to have their diagnosis of TB confirmed, patients whose first point of contact was a private clinic needed more visits than those who first visited a PHC. This higher number of visits may have been due to the poorer TB-service readiness of private clinics, most of which – particularly private solo practices – do not have appropriate facilities for TB diagnostic tests, i.e., a laboratory for sputum smear examination [17]. To solve this problem, we suggest that most clinics use sputum smear fixation and deliver the preparation for diagnosis to a referral PHC or a clinic linked with the BPJS-K [13].
Our findings also suggest that seeking care first at a private clinic or private hospital led to significantly higher costs during the pre-diagnostic phase. Except when covered by health insurance, each visit to a private hospital is costly [18, 19]. This explains why, despite the limited number of visits, high costs were incurred at private hospitals. However, while the high cost of private clinics sometimes resulted from the high costs per visit, it also may be resulted from a high number of visits or from a combination of both.
Patients who first sought care at a pharmacy, practitioner of alternative medicine or other healthcare provider had a higher number of visits than those who started care-seeking at PHCs. However, this high number of visits did not lead to significantly higher costs for diagnosis. This may have been because the costs of simple, generic medicine in a pharmacy or of consultations for alternative medicine were low.
Despite the implementation of UHC in Indonesia, excessive visits and costs during the pre-diagnostic phase remain. Although this study did not compare the situation before and after the implementation of UHC, we showed that there were no significant differences in number of visits and costs between patients who were and were not covered by national health insurance.
Excessive visits and costs can result in diagnostic delays, potential catastrophic costs during treatment, and poor outcome [10, 20]. To prevent high number of visits and high costs, the integration between the national health insurance and the NTP, which is still fragmented, should be improved [21]. Currently, there has been no direct link between the national health insurance system and the NTP. Private providers – despite linked to the BPJS-K – often unaware of the national tuberculosis guidelines and of TB referral system under the NTP [4]. The current practice of TB current guidelines in private providers seems not optimal. There has been also lack of incentives from the national health insurance to improve the quality of TB care in private sector [22]. Therefore, comprehensive strategies are imperative. To solve the fragmented system in TB care, the national health insurance needs to develop a mechanism of incentives whereby private physicians and clinics can screen and diagnose TB cases accurately and refer the case to facility where TB diagnostic tests and treatment are fully covered. In its pay-for-performance criteria [22], for example, BPJS-K should include the quality of the TB services a clinic provides. A contract of service provision that is signed between the BPJS-K and private providers should consider the readiness of the TB services including the availability of diagnostic tests, the adherence with TB management guidelines, and prior attendance of TB training. In addition, the strategies should include efforts to increase patients’ awareness, to reduce stigma and discrimination, to improve TB diagnostic options, and to increase the number of PHCs in rural districts.
This study has two main limitations. The first is our collection of data from patients who had ended up at a PHC for TB treatment, and thus our exclusion of those who had had TB treatment from a private provider. This may have led us to overestimate PHCs as the first point of contact and to underestimate the number of pre-diagnostic visits and the costs incurred during the pre-diagnostic phase. It may also have led to a misleadingly high figure for the number of visits – by at least one visit – by patients whose first point of care had not been been a PHC, particularly if this visit had involved a healthcare provider that could not itself diagnose TB. The second limitation is that, since we relied on patients’ memory to obtain the information, the number of visits and the costs incurred may also have been affected by recall bias. A patient may not remember the frequency and cost of buying medicine in a drug store or pharmacy, and thereby underestimate the number of visits and the total pre-diagnostic costs.
The provision of TB services in Indonesia is similar to health-service delivery in other high TB-burden countries in Asia that need to improve their public-private mix. However, our findings require careful generalization before being applied to other countries or even to other regions of Indonesia. As this study was conducted only on the island of Java, it does not necessarily reflect the situation throughout Indonesia.
Conclusion
Despite the UHC, high costs of TB seeking care remain, with direct medical costs contributing most to the total costs. The preference of people with TB first to seek diagnosis from a private provider rather than a PHC leads to more pre-diagnostic visits and higher costs. The UHC scheme alone is not enough to improve TB control and reduce patients’ costs. A comprehensive strategy is required to improve TB-related services in the private healthcare sectors. To reduce diagnostic delays and minimize patients’ costs, it is essential to reduce the fragmented system between the national health insurance scheme and the National TB Programme, to improve the quality of TB care in the private sector, and to improve the availability of PHCs, particularly in rural areas.
Supplementary information
Acknowledgments
We would like to thank the Heads of Jakarta Provincial Health Office, Tasikmalaya District Health Office, and Depok District Health Office for issuing permits for data collection in their districts. We also thank Dedi Suhendar, all TB Programme Officers in Primary Health Centres, and all enumerators, for their support with data collection. Finally, we thank LPDP for funding this project and USAID, SHERA, and CCR SMART CITY Universitas Indonesia for their support through the Smart City Project. TAJH was supported by a Research Excellence Initiative Grant from Erasmus University Rotterdam, The Netherlands.
Abbreviations
- BPJS-K
Badan Penyelenggara Jaminan Sosial Kesehatan (The Social Security Agency for Health)
- CI
Confidence interval
- IDR
Indonesian Rupiah
- IQR
Interquartile range
- NTP
National Tuberculosis Programme
- PHC
Primary Health Centre
- OR
Odds ratio
- cORs
Crude Odds Ratio
- aORs
Adjusted Odds Ratio
- TB
Tuberculosis
- UHC
Universal Health Coverage
- USD
US Dollar
- WHO
World Health Organization
Authors’ contributions
AF, TAJH, and JHR together conceived and developed the study design. AF led data collection in Indonesia, then ran data analysis and drafted the paper. TAJH and JHR actively supervised and contributed to data interpretation and manuscript writing. MM and EB reviewed the questionnaires that was adapted to Bahasa Indonesia, supervised data collection in Indonesia, and provided feedback to interpretation of data. All authors read and approved the final manuscript.
Funding
This study was funded by the Indonesian Endowment Fund for Education (Lembaga Pengelola Dana Pendidikan, LPDP), Indonesia. The LPDP granted a funding for the study, but did not involve and interfere in designing the study protocol, conducting data collection and data analysis, as well as finalizing the manuscript.
Availability of data and materials
Data analysed during the current study available from the corresponding author on reasonable request.
Ethics approval and consent to participate
We received ethical clearance for this study from the Ethical Committee at the Faculty of Medicine of Universitas Indonesia – Cipto Mangunkusumo Hospital, Jakarta Indonesia (No. 416/UN2.F1/ETIK/VI/2016). Before interviewing selected TB patients, we provided them with written and oral explanations, and also with the informed-consent form necessary for their approval as subjects of this study.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher’s Note
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Contributor Information
Ahmad Fuady, Email: a.fuady@erasmusmc.nl, Email: ahmad.fuady01@ui.ac.id.
Tanja A. J. Houweling, Email: a.j.houweling@erasmusmc.nl
Muchtaruddin Mansyur, Email: muchtaruddin.mansyur@ui.ac.id.
Erlina Burhan, Email: erlina_burhan@yahoo.com.
Jan Hendrik Richardus, Email: j.richardus@erasmusmc.nl.
Supplementary information
Supplementary information accompanies this paper at 10.1186/s12913-020-05350-y.
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Supplementary Materials
Data Availability Statement
Data analysed during the current study available from the corresponding author on reasonable request.