Volume 10, Issue 5 pp. 520-524

Losartan reduces the costs of diabetic end-stage renal disease: An Asian perspective

WONG KOK SENG

WONG KOK SENG

Department of Nephrology, Singapore General Hospital, Singapore,

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SHANG-JYH HWANG

SHANG-JYH HWANG

Department of Nephrology, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan,

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DONG CHEOL HAN

DONG CHEOL HAN

Renal Division, SoonChunHyang University Medical Center, Seoul, Korea,

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CHUA CHIN TEONG

CHUA CHIN TEONG

Division of Nephrology, University Malaya Medical Centre, Kuala Lumpur, Malaysia,

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JULIANA CHAN

JULIANA CHAN

Department of Medicine and Therapeutics, The Chinese University of Hong Kong, The Prince of Wales Hospital, Hong Kong, China,

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THOMAS A BURKE

Corresponding Author

THOMAS A BURKE

Merck & Co., Inc., Worldwide Outcomes Research, Whitehouse Station, NJ and

TAB, GWC and YJC are employees of Merck & Co., Inc., which manufacture and market losartan (Cozaar).

Thomas Burke, Merck & Co., Inc., Director, Worldwide Outcomes Research, One Merck Drive, WS2E-65, Whitehouse Station, NJ 08889, USA. Email: [email protected]Search for more papers by this author
GEORGE W CARIDES

GEORGE W CARIDES

Merck Research Laboratories, Blue Bell, PA, USA and

TAB, GWC and YJC are employees of Merck & Co., Inc., which manufacture and market losartan (Cozaar).

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YON JONG CHOI

YON JONG CHOI

MSD Korea, Seoul, Korea

TAB, GWC and YJC are employees of Merck & Co., Inc., which manufacture and market losartan (Cozaar).

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First published: 13 October 2005
Citations: 7

SUMMARY:

Objective:  To evaluate losartan and conventional antihypertensive therapy (CT) compared with CT alone on the cost associated with end-stage renal disease (ESRD) in Hong Kong, Japan, Korea, Malaysia, Singapore and Taiwan.

Methods:  Reduction of end-points in non-insulin-dependent diabetes mellitus with the angiotensin II antagonist losartan (RENAAL) was a multinational, double-blind, randomized, placebo-controlled trial to evaluate the renal protective effects of losartan on a background of CT in patients with type 2 diabetes and nephropathy. The primary composite end-point was a doubling of serum creatinine, ESRD or death. Data on the duration of ESRD for the Asian subgroup of patients enrolled in RENAAL were used to estimate the economic benefits of slowing the progression of nephropathy. The cost associated with ESRD was estimated by combining the number of days each patient experienced ESRD with the average daily cost of dialysis from the third-party payer perspective in Hong Kong, Japan, Korea, Malaysia, Singapore and Taiwan. Total cost, converted to US dollars, was the sum of ESRD and losartan costs.

Results:  Losartan plus CT reduced the number of days with ESRD by 37.9 per patient over 3.5 years compared with CT alone. This reduction in ESRD days resulted in a decrease in the cost associated with ESRD, which ranges from $910 to $4346 per patient over 3.5 years across the six countries or regions. After accounting for the cost of losartan, the reduction in ESRD days resulted in net savings in each of the six countries or regions, ranging from $55 to $515 per patient.

Conclusion:  Treatment with losartan in patients with type 2 diabetic nephropathy not only reduced the incidence of ESRD among Asian patients, but resulted in direct medical cost savings in countries or regions representing Asia.

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