BRONCHOSPASM ON β-BLOCKERS USED IN ASTHMATICS

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BRONCHOSPASM ON USED IN ASTHMATICS Responses to a recent report concerning nadolol Considering in retrospect the report ofa near-fatal case of bronchospasm from the nadolol [see Inpharma 277: 6 (7 Mar 1981 JJ, perhaps a more aggressive approach with salbutamol (albuteroJ) might have been attempted. A should be able to override but in normal patients a 60-fold increase in salbutamol dose is needed to achieve bronchodilation after 80mg propranolol. This means a dose of I Dmg salbutamol every 10 min by inhalation - heart rate, ECG and BP permitting. Other alternatives worth trying may be ipratropium or atropine, perhaps aminophylline, or even dinoprostone (prostaglandin E 1 ) which should bypass the effects of though it has not been tried in practice [Tatlersjield. A . E.: British Medical lournal282: 901 (J 4 Mar 1981 JJ . The dangers of in asthma are still not fully appreciated by many. The suggestion that a j3-blocker, in an :lsthmatic, should be started under medical supervision, monitoring peak flow, is wise but may not be enough, since several non-responses do not guarantee that bronchospasm may not occur later under other conditions such as with cold or exercise. Any asthmatic given a should be well versed in aerosol technique and should always carry a bronchodilator inhaler. Even then, bronchoconstriction does not always respond to perhaps because the bronchospasm is a consequence of some action other than j3-blockade, from which it follows that the cardioselective may be no safer than the non-selective ones. Skinner suggests that a possible alternative to a may be the combined a- and labetalol [Skinner. C:: British Medical lournal282: 901 (14 Mar 1981))./ And the manufacturer (Squibb) comments The report is a timely reminder of the care needed in giving any j3-blocker (cardioselective or otherwise) to any patient with a history of wheezing from any cause. Cardioselectivity is not absolute but relative and dose-dependent, and selectivity can be lost in some, even at normal therapeutic plasma levels. Several studies attest to this. Despite the selectivity of atenolol, for example, the inCidence of frequent or sporadic bronchospasm with this drug varies between 5-10 % whiie, with the non-selective nadolol, an incidence of 2 % (in 10,000 cases) has been reported. In patients with airway obstruction all should be avoided [Jackson. D.: British Medicallou rna I 282: 902 (J 4 Mar 198 I)]. The reaction to nadolol was also referred to in The Pharmaceutical Journal 226: 197 (21 Feb 1981), bringing a similar reply from the manufacturer [Woods. P.: Pharmaceutical lournal226: 290 (21 Mar 1981]..J 2 INPHARMA 28 Mar 1981 0156-2703 / 81 / 0328-0002 $00.50/ 0 © ADIS Press

Transcript of BRONCHOSPASM ON β-BLOCKERS USED IN ASTHMATICS

Page 1: BRONCHOSPASM ON β-BLOCKERS USED IN ASTHMATICS

BRONCHOSPASM ON ~-BlOCKERS USED IN ASTHMATICS

Responses to a recent report concerning nadolol Considering in retrospect the report ofa near-fatal case of bronchospasm from the ~-blocker nadolol [see Inpharma 277: 6 (7 Mar 1981 JJ, perhaps a more aggressive approach with salbutamol (albuteroJ) might have been attempted. A ~-agonist should be able to override ~-blockade, but in normal patients a 60-fold increase in salbutamol dose is needed to achieve bronchodilation after 80mg propranolol. This means a dose of I Dmg salbutamol every 10 min by inhalation - heart rate, ECG and BP permitting. Other alternatives worth trying may be ipratropium or atropine, perhaps aminophylline, or even dinoprostone (prostaglandin E1) which should bypass the effects of ~-blockade, though it has not been tried in practice [Tatlersjield. A .E.: British Medical lournal282: 901 (J 4 Mar 1981 JJ. The dangers of ~-blockade in asthma are still not fully appreciated by many. The suggestion that a j3-blocker, in an :lsthmatic, should be started under medical supervision, monitoring peak flow, is wise but may not be enough, since several non-responses do not guarantee that bronchospasm may not occur later under other conditions such as with cold or exercise. Any asthmatic given a ~-blocker should be well versed in aerosol technique and should always carry a ~-agonist bronchodilator inhaler. Even then, bronchoconstriction does not always respond to ~-agonists, perhaps because the bronchospasm is a consequence of some action other than j3-blockade, from which it follows that the cardioselective ~-blockers may be no safer than the non-selective ones. Skinner suggests that a possible alternative to a ~-blocker may be the combined a- and ~-blocker labetalol [Skinner. C:: British Medical lournal282: 901 (14 Mar 1981))./

And the manufacturer (Squibb) comments The report is a timely reminder of the care needed in giving any j3-blocker (cardioselective or otherwise) to any patient with a history of wheezing from any cause. Cardioselectivity is not absolute but relative and dose-dependent, and selectivity can be lost in some, even at normal therapeutic plasma levels. Several studies attest to this. Despite the selectivity of atenolol , for example, the inCidence of frequent or sporadic bronchospasm with this drug varies between 5-10 % whiie, with the non-selective nadolol, an incidence of 2 % (in 10,000 cases) has been reported. In patients with airway obstruction all ~-blockers should be avoided [Jackson. D.: British Medicallou rna I 282: 902 (J 4 Mar 198 I)]. The reaction to nadolol was also referred to in The Pharmaceutical Journal 226: 197 (21 Feb 1981), bringing a similar reply from the manufacturer [Woods. P.: Pharmaceutical lournal226: 290 (21 Mar 1981]..J

2 INPHARMA 28 Mar 1981 0156-2703 / 81 / 0328-0002 $00.50 / 0 © ADIS Press