The pharmacologic treatment of uncomplicated arterial hypertension in patients with airway dysfunction

被引:30
作者
Cazzola, M
Noschese, P
D'Amato, G
Matera, MG
机构
[1] Osped A Cardarelli, Unita Operat Complessa Pneumol & Allergol, Dipartimento Pneumol, Naples, Italy
[2] Univ Naples 2, Fac Med & Chirurg, Dipartimento Med Sperimentale, Naples, Italy
关键词
airway response; antihypertensive drugs; arterial hypertension; asthma; COPD;
D O I
10.1378/chest.121.1.230
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Because many antihypertensive drugs can affect airway function, the treatment of hypertension in patients with airway dysfunction is complex. For example, the worsening or precipitation of asthma by beta-adrenoceptor antagonists is well-recognized, but beta(1)-adrenoceptor blockers that exert mild beta(2)-agonist effects, and those that modulate the endogenous production of nitric oxide, affect airway function to a lesser extent. Therapy with selective alpha(1)-blockers is not contraindicated in cases of chronic airway obstruction. Conversely, alpha(2)-agonists must not be given to asthmatic subjects because they can adversely affect the bronchi. Calcium channel blockers do not exert severe side effects on the airways. Angiotensin-converting enzyme inhibitors may, cause cough and exacerbate or even induce asthma; however, angiotensin II type I (AT(1)) antagonists do not cause cough. 5-Hydroxytryptamine modifiers such as urapidil are a treatment option for patients with chronic airway obstruction. In patients with airway dysfunction, we suggest treatment with thiazide diuretics as the initial drug choice, and calcium channel blockers if the response is poor. In the case of no response, calcium channel blockers alone must be used. However, there is no strict rule because individual patients may respond differently to individual drugs and drug combinations. Consequently, it is important to adopt a flexible approach. For patients who are unresponsive to the aforementioned drugs, AT(1) receptor antagonists, newer beta(1)-adrenoceptor-blocking agents with ancillary properties (eg, celiprolol or nebivolol), and/or vasodilators can be considered.
引用
收藏
页码:230 / 241
页数:12
相关论文
共 101 条
[61]   EFFECTS OF LABETALOL AND PROPRANOLOL ON HISTAMINE-INDUCED BRONCHOCONSTRICTION IN NORMAL SUBJECTS [J].
MACONOCHIE, JG ;
WOODINGS, EP ;
RICHARDS, DA .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1977, 4 (02) :157-162
[62]   Pharmacology of nebivolol [J].
Mangrella, M ;
Rossi, F ;
Fici, F ;
Rossi, F .
PHARMACOLOGICAL RESEARCH, 1998, 38 (06) :419-431
[63]  
Marcelle R, 1996, ARCH PHYSIOL BIOCHEM, V104, P851
[64]   Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3) [J].
Mastroianni, N ;
DeFusco, M ;
Zollo, M ;
Arrigo, G ;
Zuffardi, O ;
Bettinelli, A ;
Ballabio, A ;
Casari, G .
GENOMICS, 1996, 35 (03) :486-493
[65]   Nitric oxide and airways [J].
Matera, MG .
PULMONARY PHARMACOLOGY & THERAPEUTICS, 1998, 11 (5-6) :341-348
[66]   THE BRONCHOSPARING EFFECT OF CELIPROLOL, A NEW BETA-1- ALPHA-2-RECEPTOR ANTAGONIST ON PULMONARY-FUNCTION OF PROPRANOLOL-SENSITIVE ASTHMATICS [J].
MATTHYS, H ;
DOSHAN, HD ;
RUHLE, KH ;
BRAIG, H ;
POHL, M ;
APPLIN, WJ ;
CARUSO, FS ;
NEISS, ES .
JOURNAL OF CLINICAL PHARMACOLOGY, 1985, 25 (05) :354-359
[67]   ANGIOTENSIN CONVERTING ENZYME-INHIBITORS AND COUGH [J].
MCEWAN, JR ;
FULLER, RW .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1989, 13 :S67-S69
[68]   ANGIOTENSIN-II POTENTIATES METHACHOLINE-INDUCED BRONCHOCONSTRICTION IN HUMAN AIRWAY BOTH IN-VITRO AND IN-VIVO [J].
MILLAR, E ;
NALLY, JE ;
THOMSON, NC .
EUROPEAN RESPIRATORY JOURNAL, 1995, 8 (11) :1838-1841
[69]   ACTIVITY OF THE RENIN-ANGIOTENSIN SYSTEM IN ACUTE SEVERE ASTHMA AND THE EFFECT OF ANGIOTENSIN-II ON LUNG-FUNCTION [J].
MILLAR, EA ;
ANGUS, RM ;
HULKS, G ;
MORTON, JJ ;
CONNELL, JMC ;
THOMSON, MC .
THORAX, 1994, 49 (05) :492-495
[70]  
MOHAMMED AF, 1991, CLIN DRUG INVESTIG S, V3, P196