Free Content Pharmacodynamic effects of albuterol nebulization in hospitalized COPD-patients because of an exacerbation with blocked gastrointestinal absorption

Authors: Cromheecke, H.1; Grouls, R.1; Creemers, J.2; Smeenk, F.2; Verboom, L.2; Ackerman, E.1

Source: British Journal of Clinical Pharmacology, Volume 53, Number 5, May 2002 , pp. 556P-556P(1)

Publisher: Wiley-Blackwell

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Abstract:

Despite major improvements in drug output of new nebulizers and differences between nebulizers [ 1], doses of albuterol nebulizing therapy of hospitalized COPD-patients has not changed in the last decades.

The objective was to determine the optimal dose in the current setting according to a standardized protocol (10 min at flow 8 l min−1, MICRO MIST nebulizer, Hudson RCI).

After a washout of bronchodilators patients nebulized 5 mg (group A; n=21. FEV1=47.4 ± 2.9% predicted; Tiffeneau=48.1 ± 2.5%) or 10 mg (group B; n=21, FEV1=50.5 ± 3.8% predicted; Tiffeneau=49.5 ± 3.4%) albuterol (t=−10 to 0 min). Pulmonary function (PF) (FEV1, FVC, Tiffeneau), dyspnoea (modified Borg scale) and heart-frequency (HF), blood pressure (BP), breathing-frequency (BF), serum potassium (K), fingertremor, QTc-interval, were measured at t=−30, 10, 30, 60, 120, 240 min. Charcoal was administered to prevent gastrointestinal absorption (t=−10; 10 min (5 g) and 60 min (10 g). Pharmacodynamic (PD)-effects, relative to baseline, and correlation between effects, severeness of COPD and patient characteristics were analysed.

FEV1 and FVC increased significantly (FEV1: (A) 10-120 min; (B) 10-240 min; Figure 1), leaving Tiffeneau unchanged. FVC at t=10 is significantly greater for group B compared to A (P=0.009). PD-parameters ( Table 1) showed significant changes.

All changes in group B had an earlier onset and were of the same or longer duration. Parameters not mentioned did not change clinically significant. FEV1- and dyspnoeic-changes and FEV1 and FVC changes had a significant correlation in both groups. No other correlations or differences were seen.

Group B shows no greater PF improvements, only significant and clinical relevant greater changes in some side effects. In moderate to severe COPD-patients 5 mg albuterol is the highest recommended dose, lower doses should be investigated.

Document Type: Research article

DOI: http://dx.doi.org/10.1046/j.1365-2125.2002.161321.x

Affiliations: 1: Clinical Pharmacy and 2: Pulmonology, Catharina Hospital, Eindhoven, The Netherlands

Publication date: 2002-05-01

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