Effects of Heparin on Hypertonic Potassium Chloride—Induced Bronchoconstriction
BACKGROUND: Changes in bronchial osmolarity is a well-known factor for bronchoconstriction. Recently, nonisotonic aerosols have begun to be used for the assessment of bronchial hyperreactivity. Hypertonic KCl can cause bronchoconstriction even in non-symptomatic asthmatic patients. OBJECTIVE: To eva...
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Veröffentlicht in: | The Annals of pharmacotherapy 2001-10, Vol.35 (10), p.1161-1165 |
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Sprache: | eng |
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Zusammenfassung: | BACKGROUND:
Changes in bronchial osmolarity is a well-known factor for bronchoconstriction. Recently, nonisotonic aerosols have begun to be used for the assessment of bronchial hyperreactivity. Hypertonic KCl can cause bronchoconstriction even in non-symptomatic asthmatic patients.
OBJECTIVE:
To evaluate the protective role of heparin on hypertonic KCl-induced bronchospasm in asthma.
METHODS:
Thirty-eight asthmatic patients were included in this double-blind, placebo-controlled study. On day 1 of the study, after performing the respiratory function test (RFT), patients had inhaled KCl 10% and RFTs were done after 20 minutes. On day 2 of the study, after the basal RFT, 18 patients inhaled NaCl 0.9% 0.2 mL/kg solution. After the completion of this procedure, patients waited for 20 minutes and inhaled KCl 10% 10 mL, and RFTs were repeated 20 minutes later. The second group consisted of 20 patients who inhaled heparin 1000 units/kg after the RFTs were performed. Twenty minutes later, they inhaled KCl 10% and waited for 20 minutes. Finally, RFTs were done and compared with those from the other group.
RESULTS:
In the control group, forced expiratory volume in one second (FEV1) decreased 17.4% on day 1 and 16.4% on day 2. In the heparin-treated group, FEV1 decreased 18.6% on day 1, but almost no change occurred after this group was treated with heparin before inhalation of hypertonic KCl on day 2.
CONCLUSIONS:
Heparin was found to be highly protective against hypertonic KCl—induced bronchospasm in bronchial asthma. |
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ISSN: | 1060-0280 1542-6270 |
DOI: | 10.1345/aph.10140 |