Effectiveness and safety of the angiotensin II antagonist irbesartan in children with chronic kidney diseases

被引:29
作者
Franscini, LMD
Von Vigier, RO
Pfister, R
Casaulta-Aebischer, C
Fossali, E
Bianchetti, MG [2 ]
机构
[1] Univ Milan, Sch Med, Clin De Marchi, Pediatric Renal Unit, Milan, Italy
[2] Univ Bern, Childrens Hosp,Inselspital, Kinderklin, Div Nephrol, CH-3010 Bern, Switzerland
关键词
irbesartan; chronic kidney disease; hypertension; proteinuria; childhood;
D O I
10.1016/S0895-7061(02)03083-2
中图分类号
R6 [外科学];
学科分类号
1002 [临床医学]; 100210 [外科学];
摘要
Background: Studies in adults with chronic kidney diseases demonstrate that the orally available angiotensin 11 antagonist irbesartan reduces arterial pressure and pathological proteinuria, mostly with an excellent tolerability profile. Little information is available on irbesartan in childhood. Methods: A total of 44 pediatric outpatients with chronic kidney disease (27 male and 17, aged 3.7 to 18 years, median 10 years) were given irbesartan once a day during 18 weeks for arterial hypertension (N = 23), proteinuria (N = 8), or both (N = 13). Results: In patients with hypertension, the use of irbesartan 4.1 (3.1-5.3) mg/kg body weight daily (median and interquartile range) was associated with a decrease (P < .005) in arterial pressure by 17 (13-22)/10 (7-12) mm Hg. In patients with overt proteinuria the urinary protein excretion decreased (P < .01) during treatment with irbesartan (2.9 [2.0-4-81 mg/kg body weight) by 52 (0-75) mg/[m(2) X h]), whereas plasma albumin increased (P < .05) by 4 (1-5) g/L. The frequency of abdominal pain, constipation, cough, diarrhea, dizziness, edema, fatigue, headache, insomnia, myalgia, orthostasis, and rash was similar before and with irbesartan. Plasma sodium slightly decreased, whereas plasma potassium increased, with irbesartan (P < .01). Conclusions: In pediatric patients with chronic kidney diseases, irbesartan given once a day for 18 weeks significantly reduces arterial pressure and proteinuria, with an excellent tolerability and side effect profile. (C) 2002 American Journal of Hypertension, Ltd.
引用
收藏
页码:1057 / 1063
页数:7
相关论文
共 21 条
[1]
COUGH AND CONVERTING ENZYME-INHIBITORS [J].
BIANCHETTI, MG ;
CAFLISCH, M ;
OETLIKER, OH .
EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (03) :225-226
[2]
Angiotensin II receptor antagonists [J].
Burnier, M ;
Brunner, HR .
LANCET, 2000, 355 (9204) :637-645
[3]
Pharmacologic management of childhood hypertension: Current status, future challenges [J].
Flynn, JT .
AMERICAN JOURNAL OF HYPERTENSION, 2002, 15 (02) :30S-33S
[4]
GEOMETRIC METHOD FOR MEASURING BODY-SURFACE AREA - HEIGHT-WEIGHT FORMULA VALIDATED IN INFANTS, CHILDREN, AND ADULTS [J].
HAYCOCK, GB ;
SCHWARTZ, GJ ;
WISOTSKY, DH .
JOURNAL OF PEDIATRICS, 1978, 93 (01) :62-66
[5]
Renoprotection: One or many therapies? [J].
Hebert, LA ;
Wilmer, WA ;
Falkenhain, ME ;
Ladson-Wofford, SE ;
Nahman, NS ;
Rovin, BH .
KIDNEY INTERNATIONAL, 2001, 59 (04) :1211-1226
[6]
Prevention of end-stage renal disease due to type 2 diabetes. [J].
Hostetter, TH .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (12) :910-912
[7]
A cautionary note for nephrologists: Is it time to abandon the use of dihydropyridine calcium channel blockers? [J].
Jafar, TH ;
Pereira, BJG .
SEMINARS IN DIALYSIS, 1999, 12 (03) :137-139
[8]
Angiotensin II-receptor blockers: will they replace angiotensin-converting enzyme inhibitors in the treatment of hypertension? [J].
Kaplan, NM .
JOURNAL OF HUMAN HYPERTENSION, 2000, 14 (Suppl 1) :S87-S90
[9]
Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes [J].
Lewis, EJ ;
Hunsicker, LG ;
Clarke, WR ;
Berl, T ;
Pohl, MA ;
Lewis, JB ;
Ritz, E ;
Atkins, RC ;
Rohde, R ;
Raz, I .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (12) :851-860
[10]
Mackay FJ, 1999, BRIT J CLIN PHARMACO, V47, P111