Treatment of severe intermittent claudication with PGE1 a short-term vs a long-term infusion plan a 20-week, European randomized trial analysis of efficacy and costs

被引:13
|
作者
Belcaro, G
Laurora, G
Nicolaides, AN
Agus, G
Cesarone, MR
DeSanctis, MT
Incandela, L
Ricci, A
Cazaubon, M
Ippolito, E
Barsotti, A
Vasdekis, S
Ledda, A
Iacobitti, P
Christopoulos, D
Errichi, BM
Helmis, H
Cornelli, U
Ramaswami, G
Bucci, M
Ferrari, PG
Corsi, M
Pomante, P
Mezzanotte, L
Cacchio, M
Simeone, E
Geroulakos, G
机构
[1] Univ G dAnnunzio, San Valentino PAP PEA Inst, Pescara, Italy
[2] Univ G dAnnunzio, Cardiovasc Inst, Pescara, Italy
[3] St Marys Hosp, London, England
[4] Univ London Imperial Coll Sci Technol & Med, London, England
关键词
D O I
10.1177/000331979804901103
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The efficacy, safety, and cost of prostaglandin E-1 (PGE(1)) in the treatment of severe intermittent claudication was studied by comparing a long-term treatment protocol (LTP) with a short-term treatment protocol (STP) in a randomized 20-week study. The study included 109 patients (96 completed the study) with an average total walking distance of 65.5 +/- 8 m (range 20-109). Phase 1 was a 2-week run-in phase (no treatment) for both protocols. In LTP, phase 2 was the main treatment phase. In the LTP, treatment was performed with 2-hour infusions (60 mu g PGE(1), 5 days each week for 4 weeks). In phase 3 (4-week interval period) PGE(1) was administered twice a week (same dosage). In phase 4 (monitoring lasting 3 months, from week 9 to 20) no drugs were used. In STP, phase 2 treatment was performed in 2 days by a 2-hour infusion (1st day: morning 20 mu g, afternoon 40 mu g; 2nd day morning and afternoon 60 mu g). The reduced dosage was used only at the first cycle (week 0) to evaluate reduced tolerability or side effects. Full dosage (60 mu g bid) was used for all other cycles. The same cycle was repeated at the beginning of weeks 4, 8, and 12. The observation period was between weeks 12 and 20, A treadmill test was performed at inclusion, at the beginning of each phase, and at the end of the 20th week. A similar progressive physical training plan (based on walking) and a reduction in risk factors levels plan was used in both groups. Intention-to-treat analysis indicated an increase in walking distance, which improved at 4 weeks (101.5% in STP vs 78.3% in LTP), at 8 weeks (260.9% STP vs 107.3% LTP), and at 20 weeks (351% STP vs 242% LTP). Comparable increases in pain-free walking distance were observed in the two groups. No serious drug-related side effects were observed. Local, mild adverse reactions were seen in 7% of the treated subjects in the LTP and 5% in the STP. Average cost of LTP was approximate to 6,588 ECU; for STP the average cost was approximate to 1,881 ECU. The cost to achieve an improvement in walking distance of 1 m was 35.6 ECU with the LTP and 9.45 ECU with the STP (26% of the LTP cost; p<0.02). For an average 100% increase in walking distance the LTP cost was 1,937 ECU vs 550 ECU with STP (p<0.02). The cost of PGE(1) (including infusion and operative costs) was 25% of the total cost for LTP (24.9% for STP). In summary, between-group-analysis favors STP, in terms of walking distance and costs. Results indicate good efficacy and tolerability of PGE(1) treatment. With STP less time is spent in infusion and more can be spent in the exercise program. STP reduces costs, speeds up rehabilitation, and may be used in a larger number of nonspecialized units available to follow the protocol.
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页码:885 / 894
页数:10
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