Literature DB >> 32425563

Treatment Costs for Patients with Chronic Kidney Disease Who Received Multidisciplinary Care in a District Hospital in Thailand.

Suwaporn Songsermlosakul1, Unchalee Permsuwan1, Wanchana Singhan1.   

Abstract

AIM: To estimate direct medical treatment costs in patients with pre-dialysis chronic kidney disease (CKD) in a district hospital and to analyze the factors that affected the treatment costs. PATIENTS AND METHODS: Data were retrospectively retrieved from the hospital database in the period from January 2015 to December 2017. Patients who were diagnosed with CKD and had visited ambulatory care services at least two times during the index year (January to December 2015) were included. Patients' data were excluded if they had cancer, had received renal replacement therapy, or had been referred to receive treatment at other hospitals. Treatment costs based on the providers' perspectives in the first and second years after the index year were assessed. Descriptive statistics were used to analyze patients' characteristics, and multiple linear regression was used to analyze the factors in the cost model.
RESULTS: Data of 212 patients with CKD stage G3a, G3b, or G4 who met inclusion and exclusion criteria were included for analysis. Average costs for treatment in year 1 and year 2 were not statistically different. Total cost was 5701.34 Thai Baht (THB) per year. The total cost for patients with CKD stage G4 was two times greater than for patients with CKD stage G3. Costs were increased for longer hospitalization, more frequent ambulatory visits, having diabetes mellitus or dyslipidemia as a comorbidity, and uncontrolled fasting blood glucose (FBG). A cost model with R 2=0.906 was provided. Significant predictors were length of stay, ambulatory visits, diabetes mellitus, dyslipidemia, serum creatinine, FBG, and body mass index.
CONCLUSION: Total annual treatment costs for the 2 years were not different. A more advanced stage of CKD, having diabetes mellitus or dyslipidemia as comorbidities, and uncontrolled FBG were significantly associated with increased costs for treatment in patients with pre-dialysis CKD.
© 2020 Songsermlosakul et al.

Entities:  

Keywords:  chronic kidney disease; cost; district hospital; multidisciplinary

Year:  2020        PMID: 32425563      PMCID: PMC7196240          DOI: 10.2147/CEOR.S253252

Source DB:  PubMed          Journal:  Clinicoecon Outcomes Res        ISSN: 1178-6981


Introduction

Chronic kidney disease (CKD) is a chronic disease that causes a public health burden worldwide. Global CKD prevalence is approximately 13.4%1 while it has increased to 17.7% in Thailand.2 Hypertension and diabetes mellitus are common comorbidities in CKD patients. Uncontrolled comorbidities precipitate CKD progression3,4 and lead to costly medical treatment,5–7 especially in dialysis patients.8–10 The multidisciplinary care (MDC) approach, compared with the usual care model, has shown benefits in terms of lower risk of all-cause mortality, lower rate of hospitalization, slower rate of glomerular filtration rate (GFR) decline, and less requirement for long-term dialysis.6,7,11,12 However, its benefit in cost savings is still controversial among different countries. The studies conducted in Taiwan indicated that the MDC approach has lower direct medical treatment costs for patients with advanced stages of CKD than the costs associated with usual care.6,11 A study conducted in the USA showed that the MDC approach was more cost-effective for patients with CKD stage G3 to G4 compared with usual care.7 Conversely, studies conducted in Germany reported greater direct medical costs incurred with MDC than those with usual care.13 Based on the scoping review of 40 studies in 2019,14 there is inconsistency due to various MDC team compositions. In Thailand, the MDC approach has been utilized for a decade. Thai MDC teams are composed of 2 general practitioners, 2 chronic care nurses, 1 pharmacist, 1 physical therapist, and 1 nutritionist.15 Teams are aimed at reducing the incidence of CKD and end-stage renal disease, improving patients’ quality of life, and increasing access to renal replacement therapy (RRT). From a previous randomized controlled trial in Thailand comparing integrated care with an MDC approach and usual care,16 the result shows that patients who received integrated care with MDC have better GFR over the 2 years of follow up. However, studies related to costs and outcomes of the MDC approach are still limited; therefore, this study aimed to estimate the direct medical treatment costs for patients with pre-dialysis CKD in Thailand.

Patients and Methods

Study Design and Patients

This retrospective cohort study was conducted at a public district hospital in Kamphaengphet province, Thailand. MDC members of CKD clinic in this setting comprised of 1 general practitioner, 2 nurses, 1 pharmacist, 1 dietician, and 1 physical therapist. There was also a home visit team that provide health care at patients’ homes for every 3 months. Home visit team members comprised of 2 nurses or public health officers and at least 3 village health volunteers. Patients included in the study were aged 18 years or above, had been diagnosed with CKD (ICD 10 N138, N184 and N185) according to eGFR calculated by CKD-EPI equation, regularly received treatment at the aforementioned hospital, and had visited ambulatory care services at least two times during the index year (January to December 2015). Serum creatinine or GFR data were required to confirmed CKD stage. Patients were excluded if they met at least one of the following criteria: 1) were diagnosed with having cancer, 2) received RRT including chronic intermittent hemodialysis or peritoneal dialysis, 3) had been referred to other hospitals, or 4) were lost to follow up or death. CKD stages were classified by the recommendation of Kidney Disease Improving Global Outcomes (KDIGO).17 GFR was calculated using the CKD-EPI equation.18 The study protocol was in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of Faculty of Pharmacy, Chiang Mai University (No. 010/2561). Since the hospital database was retrospectively retrieved in this study, written informed consent was not obtained from an individual patient. Code numbers were used in data collection to prevent individual identification and maintain patients’ confidentiality.

Data Collection

Data were retrieved from the hospital database for 3 years starting from January 2015 to December 2017. The first year would be the index year. Patients who had visited the hospital in the index year and met the inclusion and exclusion criteria above would be included in this study. Demographic and clinical data of those included patients were collected in the first year; then costs would be collected for the next 2 years. Resource uses of these following items for both ambulatory care and in-patient care such as medications, parenteral nutrition, medical supplies, blood products, laboratory tests, and other medical services were collected. Unit costs of the items above were obtained from the standard unit cost list for medical and health services in Thailand.19

Cost Estimation

This study considered the health-care provider’s perspective. Therefore, only direct medical costs were included. Direct medical costs comprised of cost in diagnosis, laboratory test, pharmacological and non-pharmacological treatment, and services for ambulatory care in outpatient clinics and emergency room, and hospitalization care. The cost estimation was analyzed by the multiplication of unit cost times the number of uses. Total cost was the summation of all cost items. Ambulatory cost was calculated for all patients, but hospitalization cost was calculated only for admitted patients. Costs were inflated using Thailand’s consumer price index20 and presented in the year 2019.

Statistical Analysis

Patients’ characteristics and clinical data were reported as descriptive statistics. Annual costs of different years and patients’ characteristics were analyzed using the Independent t-test or the analysis of variance test as appropriate. Multiple linear regression analysis was used for forecasting cost models in CKD patient care. Stepwise method was used to plugged variables in the model. Statistical analyses were executed using SPSS 17.0 (SPSS, Chicago, IL, USA) and statistical significance was considered if P < 0.05.

Results

A total of 331 patients were eligible based on inclusion criteria. However, 116 patients were excluded due to the following reasons: 1) referral to other settings (53 patients), 2) having cancer (52 patients), 3) receiving RRT (11 patients), and 4) loss to follow up or death (3 patients). Therefore, 212 patients with CKD stage G3 to G4 were included in the analysis. The average age was 69.42 years and 35.40% were male. Hypertension (93.90%) was the most common comorbidity found in this group of patients. Diabetes mellitus was doubled in patients with CKD stage G4 compared with patients with CKD stage G3. Of the 41 total admissions, patients with stage G3a, G3b, and G4 were accounted for at 20 (48.78%), 12 (29.27%), and 9 (21.95%), respectively. Patients’ characteristics are shown in Table 1.
Table 1

Patients’ Characteristics

CharacteristicsCKD G3a (n=123)CKD G3b (n=67)CKD G4 (n=22)All (n=212)P-value
Male sex (n)50 (40.70)17 (25.40)8 (36.40)75 (35.40)0.110
Age (years)68.11 ± 10.0572.00 ± 9.7068.82 ± 10.5269.42 ± 10.100.038*
 <6544 (35.80)15 (22.40)8 (36.40)67 (31.60)
 ≥6579 (64.20)52 (77.60)14 (63.60)145 (68.40)
Hypertension (n)117 (95.10)64 (95.50)18 (81.80)199 (93.90)0.045*
Diabetes mellitus (n)37 (30.10)23 (34.30)14 (63.60)74 (34.90)0.009*
Dyslipidemia (n)61 (49.60)31 (46.30)13 (59.10)105 (49.50)0.584
MI/CHF (n)1 (0.80)3 (4.50)2 (9.10)6 (2.80)0.060
Length of stay (day)1.19 ± 0.451.19 ± 0.441.50 ± 0.671.29 ± 0.680.001*
 0103 (83.74)55 (82.09)13 (59.08)171 (80.70)
 1–717 (13.82)11 (16.42)7 (31.82)35 (16.50)
 ≥83 (2.44)1 (1.49)2 (9.10)6 (2.80)
Ambulatory visit (visit)6.55 ± 2.746.22 ± 2.216.32 ± 1.966.42 ± 2.500.674
 1–415 (12.20)11 (16.40)3 (13.60)29 (13.70)
 5–782 (66.70)44 (65.70)13 (59.10)139 (65.60)
 ≥826 (21.10)12 (17.90)6 (27.30)44 (20.80)
BMI (kg/m2)23.94 ± 3.8523.77 ± 4.9223.93 ± 3.5523.89 ± 4.170.962
SBP (mmHg)140.38 ± 14.42140.54 ± 13.67141.59 ± 15.51140.55 ± 14.240.935
FBG (mg/dL)103.41 ± 28.63109.10 ± 41.98121.11 ± 25.60107.04 ± 33.470.060
HbA1c (%), n=746.46 ± 0.847.10 ± 1.706.80 ± 1.306.72 ± 1.260.151
 <7%29 (78.40)13 (56.50)7 (50.00)49 (66.20)
 ≥7%8 (21.60)10 (43.50)7 (50.00)25 (33.80)
TG (mg/dL)159.82 ± 83.65165.69 ± 119.90180.34 ± 79.79163.81 ± 96.000.643
LDL (mg/dL)114.80 ± 31.31110.48 ± 39.13120.89 ± 39.76114.07 ± 34.820.449
HDL (mg/dL)45.82 ± 11.7643.80 ± 8.6842.18 ± 10.5844.80 ± 10.780.227
BUN (mg/dL)16.65 ± 4.9722.28 ± 12.5429.12 ± 7.7719.72 ± 9.29<0.001*
Scr (mg/dL)1.20 ± 0.171.45 ± 0.212.29 ± 0.561.39 ± 0.41<0.001*
eGFR (mL/min/1.73m2)53.11 ± 3.4139.43 ± 4.0225.08 ± 6.3345.88 ± 10.23<0.001*

Note: *P-value <0.05.

Abbreviations: BMI, body mass index; BUN, blood urea nitrogen; CHF, chronic heart failure; CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate; FBG, fasting blood glucose; HbA1c, hemoglobin A1c; HDL, high-density lipoprotein cholesterol; LDL, low-density lipoprotein cholesterol; MI, myocardial infarction; SBP, systolic blood pressure; Scr, serum creatinine; TG, triglyceride; CKD G3a, chronic kidney disease stage G 3a (GFR 45–59 mL/min/1.73 m2); CKD stage 3b, chronic kidney disease stage G 3b (GFR 30–44 mL/min/1.73 m2); CKD G4, chronic kidney disease stage G 4 (GFR 15–29 mL/min/1.73 m2).

Patients’ Characteristics Note: *P-value <0.05. Abbreviations: BMI, body mass index; BUN, blood urea nitrogen; CHF, chronic heart failure; CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate; FBG, fasting blood glucose; HbA1c, hemoglobin A1c; HDL, high-density lipoprotein cholesterol; LDL, low-density lipoprotein cholesterol; MI, myocardial infarction; SBP, systolic blood pressure; Scr, serum creatinine; TG, triglyceride; CKD G3a, chronic kidney disease stage G 3a (GFR 45–59 mL/min/1.73 m2); CKD stage 3b, chronic kidney disease stage G 3b (GFR 30–44 mL/min/1.73 m2); CKD G4, chronic kidney disease stage G 4 (GFR 15–29 mL/min/1.73 m2). Table 2 shows that the average total treatment costs in year 1 and year 2 were 5701.34 and 5697.24 THB per year, respectively. Total costs were divided into ambulatory and hospitalization costs. It was found that ambulatory costs were greater than hospitalization costs for both years. However, total costs in year 1 and year 2 were not statistically significantly different (P > 0.05).
Table 2

Treatment Cost by Chronic Kidney Disease Stages (per Year)

CostCKD Stage G3a (n=123)CKD Stage G3b (n=67)CKD Stage G4 (n=22)All (n=212)
Mean ± SDDiffP-valueMean ± SDDiffP-valueMean ± SDDiffP-valueMean ± SDDiffP-value
Ambulatory Cost
 Year 1 THB3843.01 ± 1697.6312.420.9294407.83 ± 3238.75156.580.2356353.90 ± 3551.12−98.890.8514282.08 ± 2601.4346.430.658
 (USD)(117.13 ± 51.74)(0.38)(134.34 ± 98.71)(4.78)(193.66 ± 108.23)(−3.02)(130.51 ± 79.29)(1.41)
 Year 2 THB3855.43 ± 1642.644564.41 ± 2926.206255.00 ± 2901.364328.51 ± 2368.84
 (USD)(117.51 ± 50.06)(139.12 ± 89.18)(190.64 ± 88.43)(131.92 ± 8.19)
Hospitalization Costs (All Cases)
 Year 1 THB1070.58 ± 3353.69−260.300.4111066.23± 2974.421144.280.1064443.83 ± 6956.42−2516.420.1261419.26 ± 3892.43−50.520.880
 (USD)(32.63 ± 102.21)(−7.93)(32.50 ± 90.66)(34.87)(135.44 ± 212.02)(76.7)(43.26 ± 118.63)(−1.54)
 Year 2 THB810.28 ± 2169.132210.51 ± 6503.921927.41 ± 3242.371368.74 ± 4175.85
 (USD)(24.70 ± 66.11)(67.37 ± 198.23)(58.74 ± 98.82)(41.72 ± 127.27)
Hospitalization Cost (only Admitted Patients)
 Year 1 THB(n=20) 6584.08 ± 5831.56−1838.150.209(n=12) 5953.11 ± 4620.216388.920.074(n=9) 10,862.70 ± 6970.38−4805.130.109(n=41) 7338.62 ± 5949.43−84.320.954
 (USD)(200.67 ± 177.74)(−56.02)(181.44 ± 140.82)(144.28)(331.08 ± 212.44)(−146.46)(223.67 ± 181.33)(−2.57)
 Year 2 THB(n=21) 4745.93 ± 3014.80(n=12) 12,342.03 ± 10,834.89(n=7) 6057.57 ± 2758.04(n=40) 7254.30 ± 7110.02
 (USD)(144.65 ± 91.88)(376.16 ± 330.23)(184.62 ± 84.06)(221.10 ± 216.70)
Total Cost
 Year 1 THB4913.59 ± 4266.90−247.880.5295474.06 ± 5230.631300.860.06810,797.73 ± 8950.33−2615.310.1875701.34 ± 5490.35−4.100.991
 (USD)(149.76 ± 130.05)(−7.56)(166.84 ± 159.42)(39.65)(329.10 ± 272.79)(−79.72)(173.77 ± 167.34)(−0.13)
 Year 2 THB4665.71 ± 3027.526774.92 ± 7976.688182.41 ± 5235.815697.24 ± 5437.23
 (USD)(142.20 ± 92.27)(206.49 ± 243.12)(249.38 ± 159.58)(173.64 ± 165.72)

Notes: 1 THB = 0.03048 USD (exchange rate from Bank of Thailand on March 30, 2020). Diff, difference which calculated by cost in year 1 minus cost in year 2; P, p-value; CKD stage 3a, GFR 45–59 mL/min/1.73 m2; CKD stage 3b, GFR 30–44 mL/min/1.73 m2; CKD stage 4, GFR 15–29 mL/min/1.73 m2.

Abbreviations: SD, standard deviation; CKD, chronic kidney disease.

Treatment Cost by Chronic Kidney Disease Stages (per Year) Notes: 1 THB = 0.03048 USD (exchange rate from Bank of Thailand on March 30, 2020). Diff, difference which calculated by cost in year 1 minus cost in year 2; P, p-value; CKD stage 3a, GFR 45–59 mL/min/1.73 m2; CKD stage 3b, GFR 30–44 mL/min/1.73 m2; CKD stage 4, GFR 15–29 mL/min/1.73 m2. Abbreviations: SD, standard deviation; CKD, chronic kidney disease. Ambulatory costs for patients aged less than 65 years were higher than those of patients aged more than 65 years (4902.94 and 3995.19 THB per year, P=0.018). Ambulatory costs, hospitalization costs, and total costs for treatment were higher for patients who had been hospitalized, especially those who had lengths of stay for more than 8 days, as opposed to those who had not been hospitalized. Costs were also higher for patients who had visited ambulatory services more than eight times per year, had diabetes mellitus as a comorbidity, and/or uncontrolled fasting blood glucose (FBG) which is defined as FBG > 130 mg/dL. Treatment costs by patients’ characteristics are shown in Table 3 and .
Table 3

Treatment Costs by Patients’ Characteristics (THB per Year)

CharacteristicsAmbulatory Cost (n=212)Hospitalization Cost (n=41)Total Cost (n=212)
Mean ± SDDifferenceP-valueMean ± SDDifferenceP-valueMean ± SDDifferenceP-value
Age (years)
 <654902.94 ± 3405.33−907.750.018*9545.47 ± 8838.39−2918.740.1816327.64 ± 7220.89−915.700.260
 ≥653995.19 ± 2083.036626.73 ± 4648.885411.94 ± 4472.62
Length of Stay (days)
 04002.04 ± 1940.27Reference4002.04 ± 1940.27Reference
 1–74547.37 ± 4586.44545.320.4283903.96 ± 1550.772465.140.1829979.88 ± 5068.615977.84<0.001*
 ≥810,715.47 ± 7697.896713.43<0.001*6369.09 ± 5265.0929,173.01 ± 9021.0725,170.97<0.001*
Ambulatory Visit
 1–42527.25 ± 1483.11Reference3903.95 ± 3101.54Reference3065.73 ± 2233.43Reference
 5–74176.08 ± 2013.181648.830.003*6369.09 ± 5265.092465.140.4475046.68 ± 3807.181980.950.142
 ≥85773.50 ± 3792.003246.25<0.001*9125.26 ± 6710.315221.310.1149506.57 ± 8789.966440.84<0.001*
CKD Stage
 G3a3843.01 ± 1697.63Reference6584.08 ± 5831.56Reference4913.59 ± 4266.90Reference
 G3b4407.83 ± 3238.75564.820.2995953.11 ± 4620.21−630.970.7675474.06 ± 5230.63560.470.076
 G46353.90 ± 3551.432510.89< 0.001*10,862.70 ± 6970.384278.620.07310,797.73 ± 8950.335884.14<0.001*
Diabetes Mellitus
 No3352.95 ± 1390.182661.82<0.001*5598.83 ± 3794.463754.280.042*4245.52 ± 3133.924170.73<0.001*
 Yes6014.77 ± 3355.369353.10 ± 7340.058416.24 ± 7564.27
Dyslipidemia
 No3759.87 ± 1924.761054.360.003*7121.05 ± 6438.63594.690.7625490.22 ± 5624.31426.260.573
 Yes4814.23 ± 3063.937715.74 ± 5182.835916.48 ± 5368.77
Hypertension
 No3276.24 ± 2057.611071.540.1514585.05 ± 4015.542970.950.4124334.33 ± 3578.071456.310.355
 Yes4347.78 ± 2623.827556.00 ± 6060.595790.64 ± 5587.17
SBP (mmHg)
 <1404603.53 ± 3108.22−577.520.0687771.54 ± 6105.70−682.680.7285843.66 ± 5857.02−321.810.703
 ≥1404026.00 ± 2091.917088.86 ± 5964.835587.96 ± 5202.42
DBP (mmHg)
 <904300.28 ± 2678.46−35.810.9537309.20 ± 6139.521635.260.6095677.93 ± 5539.30375.430.772
 ≥904264.48 ± 1701.448944.45 ± 4375.186053.37 ± 5237.80
LDL (mg/dL)
 <1004433.17 ± 2307.64−368.190.5075661.73 ± 3591.882750.090.1515551.54 ± 3740.60242.420.756
 ≥1004188.65 ± 2772.008411.82 ± 6917.725793.96 ± 6347.66
HDL (mg/dL)
 <604049.17 ± 1693.96258.510.6674723.94 ± 2162.583062.910.2495398.59 ± 3199.23335.730.791
 ≥604307.68 ± 2684.537786.85 ± 6288.165734.59 ± 5690.96
TG (mg/dL)
 <2004206.30 ± 2655.47303.120.4646847.94 ± 6120.102514.690.2895627.57 ± 5565.77295.080.736
 ≥2004509.42 ± 2442.169362.64 ± 5021.795922.17 ± 5303.17
Hemoglobin A1c (%)
 <75428.80 ± 3159.081734.470.035*9840.34 ± 7797.68−1029.670.7707437.16 ± 7211.252898.100.120
 ≥77163.27 ± 3494.268811.07 ± 7224.2310,335.26 ± 8015.06
FBG (mg/dL)
 <1303888.79 ± 1871.022779.19<0.001*6528.22 ± 5178.294153.310.0765072.48 ± 4249.674443.91<0.001*
 ≥1306667.98 ± 4531.0110,681.52 ± 7988.239516.39 ± 9437.57

Notes: * P-value <0.05. Mean ±SD, mean ± standard deviation.

Abbreviations: DBP, diastolic blood pressure; FBG, fasting blood glucose; HDL, high-density lipoprotein cholesterol; LDL, low-density lipoprotein cholesterol; SBP, systolic blood pressure; TG, triglyceride; CKD G3a, chronic kidney disease stage G 3a (GFR 45–59 mL/min/1.73 m2); CKD stage 3b, chronic kidney disease stage G 3b (GFR 30–44 mL/min/1.73 m2); CKD G4, chronic kidney disease stage G 4 (GFR 15–29 mL/min/1.73 m2); HDL, high-density lipoprotein; LDL, low-density lipoprotein.

Treatment Costs by Patients’ Characteristics (THB per Year) Notes: * P-value <0.05. Mean ±SD, mean ± standard deviation. Abbreviations: DBP, diastolic blood pressure; FBG, fasting blood glucose; HDL, high-density lipoprotein cholesterol; LDL, low-density lipoprotein cholesterol; SBP, systolic blood pressure; TG, triglyceride; CKD G3a, chronic kidney disease stage G 3a (GFR 45–59 mL/min/1.73 m2); CKD stage 3b, chronic kidney disease stage G 3b (GFR 30–44 mL/min/1.73 m2); CKD G4, chronic kidney disease stage G 4 (GFR 15–29 mL/min/1.73 m2); HDL, high-density lipoprotein; LDL, low-density lipoprotein. Although 15 variables of patients’ characteristics and clinical data obtained from the hospital database were plugged into the cost model, 6 variables demonstrated significant predictors at P-value <0.05. Those were age, length of stay, ambulatory visits, body mass index, diabetes mellitus, and FBG (Table 4 and ).
Table 4

Cost Model of Chronic Kidney Disease Treatment

Unstandardized CoefficientstSig.95% Confidence Interval for B
BSELower BoundUpper Bound
Constant−5072.638924.560−5.487<0.001−6895.557−3249.720
Length of stay2191.77665.02333.708<0.0012063.5732319.980
Ambulatory visit456.56050.9368.963<0.001356.131556.989
Diabetes mellitus1290.311303.5504.251<0.001691.8131888.808
Dyslipidemia719.157245.6772.9270.004234.7651203.550
Serum creatinine1672.233290.7725.751<0.0011098.9302245.536
Fasting blood glucose9.9824.2592.3440.0201.58418.380
Body mass index86.73728.7773.0140.00329.998143.476

Notes: Adjusted R2 = 0.906; probability of F-test <0.001

Abbreviations: SE, standard error; Sig., significance.

Cost Model of Chronic Kidney Disease Treatment Notes: Adjusted R2 = 0.906; probability of F-test <0.001 Abbreviations: SE, standard error; Sig., significance.

Discussion

The study estimated the direct medical costs for standard treatment with the MDC approach in patients with CKD stage G3 to G4 who received treatment at a district hospital. In Thailand, patients with an advanced CKD stage or who need RRT are referred to receive treatment with nephrologists at tertiary hospitals; hence, only CKD stages G3 and G4 patients receive treatment at district hospitals. The average age of our sample population was 69.42 years, which was older than those in other studies.6,11,16 We found that all samples remained in the same CKD stage and received the same standard treatment over the 2 years. This led to no statistically significant difference in the estimated treatment costs. More severe stages of CKD resulted in higher treatment costs. Although treatment costs for patients with CKD stage G3a and G3b were not different, it was doubled in patients with CKD stage G4 due to a higher hospitalization rate (16.26%, 17.91%, and 40.92% for patients with stage G3a, G3b, and G4, respectively). This finding was concordant with previous studies that estimated direct medical costs for treatment with the MDC approach.7,13 The cost model showed that ambulatory visits, hospitalization, diabetes mellitus, dyslipidemia, serum creatinine, FBG, and body mass index are the main cost drivers. The more frequent ambulatory visits, the longer the hospitalization, having diabetes mellitus or dyslipidemia as a comorbidity, having higher serum creatinine or FBG, and greater body mass index independently increase treatment costs. One-third of these CKD patients had diabetes mellitus and treatment costs were doubled compared to those with no diabetes mellitus. This might be due to a longer duration of hospitalization (1.20 vs 0.46 days) and more frequent ambulatory visits (6.81 vs 6.22 visits). Unexpectedly, patients with both CKD and diabetes mellitus who achieved the hemoglobin A1c (HbA1c) target had no significant difference in treatment costs compared with those who did not achieve the HbA1c target. This might be attributable to a small sample size (Table 1) and criteria. Due to FBG monitoring being more convenient and less expensive than HbA1c monitoring, it can be measured more frequently in district hospitals. We found that treatment costs for patients with uncontrolled FBG were substantially higher than for those who met the recommended FBG target of <130 mg/dL.21 About half of the patients had dyslipidemia as a comorbidity. Patients with dyslipidemia had slightly higher treatment costs than those without dyslipidemia. The difference in treatment costs was mainly from drug costs instead of laboratory monitoring, frequency of ambulatory visits, length of hospitalization, or CKD stage. Again, drug costs were the major component that affected the treatment costs for patients with serum creatinine ≥2 mg/dL compared with those with serum creatinine less than 2 mg/dL. All patients with serum creatinine ≥2 mg/dL, 92.31% were categorized into CKD stage G4. Ambulatory costs for patients aged less than 65 years were higher than those of patients aged more than 65 years. This finding was in line with results of the study conducted in Italy by Turchetti and colleagues.22 They reported that CKD patients aged more than 74 years had lower direct medical cost compared to those who aged less than 74 years due to lower costs of diagnostic exams, laboratory tests and hospital cares.22 A previous cost-effectiveness study of MDC in CKD patients in Thailand reported direct medical costs of 6265.86 THB per year22 (presented in the year 2019), which was slightly greater than our finding (5701.34 THB per year). Srisubat et al23 estimated total costs using unit costs from a district hospital while our study used the accepted national standard unit costs in Thailand.19 Various sources of unit costs might lead to unequal results. Based on our findings, treatment costs do not fluctuate with the implementation of the MDC approach in a district hospital. This might reflect stable clinical status of patients who benefit from MDC. Our results are quite in line with the clinical pieces of evidence from meta-analysis12 and other studies6,7,11 that report a lower risk of hospitalization and GFR decline. Approximately 20% of pre-dialysis CKD patients reached end-stage renal disease (ESRD) within 4–6 years.24,25 Most CKD patients also had at least 1 common comorbidity such as diabetes mellitus, dyslipidemia or cardiovascular disease and suffered from many complications. These patients should be referred to receive treatment with the nephrologist. Some strengths are needed to mention. Even though our center is a community hospital, the MDC team has established for several years due to the readiness of the collaboration among healthcare teams. This leads to a number of CKD patients regularly visiting the MDC clinic each week. In addition, we have the completed data for analyses in this study. Our study has some limitations. We did not compare the treatment costs of the MDC approach with treatment costs of usual care. This is still a gap for a further experimental study comparing these two approaches, analyzing their benefits in terms of cost and effectiveness. Since this study conducted in a single center in Thailand, the generalizability of our findings to other countries might be limited. However, we believe that in the country that has CKD patient care similar to our study and would like to establish an MDC team, our findings might provide some useful information.

Conclusion

Total annual treatment costs for 2 years were not different. A more advanced stage of CKD, having diabetes mellitus or dyslipidemia as comorbidities, and uncontrolled fasting blood glucose were significantly associated with increased costs for treatment in patients with pre-dialysis CKD.
  22 in total

1.  Educational intervention in CKD retards disease progression and reduces medical costs for patients with stage 5 CKD.

Authors:  Chen-Chou Lei; Pei-Hsien Lee; Yung-Chien Hsu; Hung-Yu Chang; Chun-Wu Tung; Ya-Hsueh Shih; Chun-Liang Lin
Journal:  Ren Fail       Date:  2012-10-22       Impact factor: 2.606

2.  US Renal Data System 2019 Annual Data Report: Epidemiology of Kidney Disease in the United States.

Authors:  Rajiv Saran; Bruce Robinson; Kevin C Abbott; Jennifer Bragg-Gresham; Xiaoying Chen; Debbie Gipson; Haoyu Gu; Richard A Hirth; David Hutton; Yan Jin; Alissa Kapke; Vivian Kurtz; Yiting Li; Keith McCullough; Zubin Modi; Hal Morgenstern; Purna Mukhopadhyay; Jeffrey Pearson; Ronald Pisoni; Kaitlyn Repeck; Douglas E Schaubel; Ruth Shamraj; Diane Steffick; Megan Turf; Kenneth J Woodside; Jie Xiang; Maggie Yin; Xiaosong Zhang; Vahakn Shahinian
Journal:  Am J Kidney Dis       Date:  2019-11-05       Impact factor: 8.860

3.  Standard cost lists for health economic evaluation in Thailand.

Authors:  Arthorn Riewpaiboon
Journal:  J Med Assoc Thai       Date:  2014-05

4.  Incremental cost-effectiveness analysis of a multidisciplinary renal education program for patients with chronic renal disease.

Authors:  Carla Sabariego; Eva Grill; Mirjam Brach; Emanuel Fritschka; Jarmila Mahlmeister; Gerold Stucki
Journal:  Disabil Rehabil       Date:  2010       Impact factor: 3.033

5.  Short-term blood pressure variability in nondialysis chronic kidney disease patients: correlates and prognostic role on the progression of renal disease.

Authors:  Silvio Borrelli; Carlo Garofalo; Francesca Mallamaci; Giovanni Tripepi; Giovanna Stanzione; Michele Provenzano; Giuseppe Conte; Luca De Nicola; Carmine Zoccali; Roberto Minutolo
Journal:  J Hypertens       Date:  2018-12       Impact factor: 4.844

6.  Multidisciplinary care improves clinical outcome and reduces medical costs for pre-end-stage renal disease in Taiwan.

Authors:  Yue-Ren Chen; Yu Yang; Shu-Chuan Wang; Wen-Yu Chou; Ping-Fang Chiu; Ching-Yuang Lin; Wen-Chen Tsai; Jer-Ming Chang; Tzen-Wen Chen; Shyang-Hwa Ferng; Chun-Liang Lin
Journal:  Nephrology (Carlton)       Date:  2014-11       Impact factor: 2.506

Review 7.  Global Prevalence of Chronic Kidney Disease - A Systematic Review and Meta-Analysis.

Authors:  Nathan R Hill; Samuel T Fatoba; Jason L Oke; Jennifer A Hirst; Christopher A O'Callaghan; Daniel S Lasserson; F D Richard Hobbs
Journal:  PLoS One       Date:  2016-07-06       Impact factor: 3.240

8.  Healthcare costs in chronic kidney disease and renal replacement therapy: a population-based cohort study in Sweden.

Authors:  Jonas K Eriksson; Martin Neovius; Stefan H Jacobson; Carl-Gustaf Elinder; Britta Hylander
Journal:  BMJ Open       Date:  2016-10-07       Impact factor: 2.692

9.  End-stage renal disease-financial costs and years of life lost in Panama: a cost-analysis study.

Authors:  Ilais Moreno Velásquez; Maribel Tribaldos Causadias; Régulo Valdés; Beatriz Gómez; Jorge Motta; César Cuero; Víctor Herrera-Ballesteros
Journal:  BMJ Open       Date:  2019-05-27       Impact factor: 2.692

10.  Cost-effectiveness of multidisciplinary care in mild to moderate chronic kidney disease in the United States: A modeling study.

Authors:  Eugene Lin; Glenn M Chertow; Brandon Yan; Elizabeth Malcolm; Jeremy D Goldhaber-Fiebert
Journal:  PLoS Med       Date:  2018-03-27       Impact factor: 11.069

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  1 in total

1.  The economic burden of diabetic retinopathy care at a tertiary eye care center in South India.

Authors:  Andrea Orji; Padmaja K Rani; Raja Narayanan; Niroj K Sahoo; Taraprasad Das
Journal:  Indian J Ophthalmol       Date:  2021-03       Impact factor: 1.848

  1 in total

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