Literature DB >> 9407424

Long-term progression of chronic renal insufficiency in the AIPRI Extension Study. The Angiotensin-Converting-Enzyme Inhibition in Progressive Renal Insufficiency Study Group.

F Locatelli1, I R Carbarns, G Maschio, J F Mann, C Ponticelli, E Ritz, D Alberti, M Motolese, G Janin, P Zucchelli.   

Abstract

The Angiotensin-converting-enzyme Inhibition on Progressive Renal Insufficiency (AIPRI) Study showed that the ACE inhibitor benazepril provides protection against loss of renal function in patients with chronic renal insufficiency (CRI) caused by various renal diseases. As a result of unexpectedly low mortality in the placebo group, there was a substantial imbalance in mortality during the course of this study (8 patients on benazepril vs. 1 on placebo). The aim of the extension study was to follow-up the patients from the AIPRI core study until autumn 1996, focusing on CRI progression and mortality. Data collection was post hoc. Patients were treated according to investigators' usual practices, without knowledge of the core study trial medication or (initially) the core trial results. A new primary efficacy parameter was defined as the time from the start of core study treatment to the occurrence of the first event in the combined composite end-point of dialysis, renal transplantation or death related to renal disease. Serial serum creatinine levels and all-cause mortality were also recorded. The median total follow-up for core + extension periods was 6.6 years. Many patients from both treatment groups (64% on benazepril and 61% on placebo) received ACE inhibitors during follow-up. In the intention-to-treat analysis of the core + extension data, only 79 of 300 patients from the benazepril group, compared to 102 of the 283 patients from the placebo group needed dialysis or renal transplantation, or died related to renal disease (P < 0.013, log-rank test). The mortality imbalance seen in the core trial was not evident with the longer follow-up (25 deaths in the benazepril and 23 in the placebo group, before dialysis). These data clearly demonstrate a long-term beneficial effect in patients randomized to take benazepril during the core study, but because treatment during the extension period was not randomized, the results of this intention-to-treat analysis need to be interpreted with care.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9407424

Source DB:  PubMed          Journal:  Kidney Int Suppl        ISSN: 0098-6577            Impact factor:   10.545


  10 in total

Review 1.  Angiotensin converting enzyme inhibition: from viper to patient.

Authors:  M Komajda; M C Wimart
Journal:  Heart       Date:  2000-09       Impact factor: 5.994

2.  Antihypertensive treatment with and without benazepril in patients with chronic renal insufficiency: a US economic evaluation.

Authors:  Thomas J Hogan; William J Elliott; Arnold H Seto; George L Bakris
Journal:  Pharmacoeconomics       Date:  2002       Impact factor: 4.981

Review 3.  The RAAS in the pathogenesis and treatment of diabetic nephropathy.

Authors:  Piero Ruggenenti; Paolo Cravedi; Giuseppe Remuzzi
Journal:  Nat Rev Nephrol       Date:  2010-05-04       Impact factor: 28.314

4.  Clinical problem solving based on the 1999 Canadian recommendations for the management of hypertension.

Authors:  R D Feldman; N R Campbell; P Larochelle
Journal:  CMAJ       Date:  1999       Impact factor: 8.262

5.  1999 Canadian recommendations for the management of hypertension. Task Force for the Development of the 1999 Canadian Recommendations for the Management of Hypertension.

Authors:  R D Feldman; N Campbell; P Larochelle; P Bolli; E D Burgess; S G Carruthers; J S Floras; R B Haynes; G Honos; F H Leenen; L A Leiter; A G Logan; M G Myers; J D Spence; K B Zarnke
Journal:  CMAJ       Date:  1999       Impact factor: 8.262

Review 6.  Renin-angiotensin-aldosterone system blockade in chronic kidney disease: current strategies and a look ahead.

Authors:  Francesca Viazzi; Barbara Bonino; Francesca Cappadona; Roberto Pontremoli
Journal:  Intern Emerg Med       Date:  2016-03-17       Impact factor: 3.397

Review 7.  Renal protection and antihypertensive drugs: current status.

Authors:  A Salvetti; P Mattei; I Sudano
Journal:  Drugs       Date:  1999-05       Impact factor: 9.546

8.  Effects of angiotensin-converting enzyme inhibitors in systolic heart failure patients with chronic kidney disease: a propensity score analysis.

Authors:  Ali Ahmed; Thomas E Love; Xuemei Sui; Michael W Rich
Journal:  J Card Fail       Date:  2006-09       Impact factor: 5.712

9.  Protection of Renal Function with ACE Inhibitors: Experience with Benazepril.

Authors:  J C Aldigier; Y L Meur; P Brunel
Journal:  Clin Drug Investig       Date:  1998       Impact factor: 2.859

Review 10.  Interventions for preventing the progression of autosomal dominant polycystic kidney disease.

Authors:  Davide Bolignano; Suetonia C Palmer; Marinella Ruospo; Carmine Zoccali; Jonathan C Craig; Giovanni F M Strippoli
Journal:  Cochrane Database Syst Rev       Date:  2015-07-14
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.