| Literature DB >> 21985340 |
Francesco De Blasio1, Johann C Virchow, Mario Polverino, Alessandro Zanasi, Panagiotis K Behrakis, Gunsely Kilinç, Rossella Balsamo, Gianluca De Danieli, Luigi Lanata.
Abstract
Cough is one of the most common symptoms for which patients seek medical attention from primary care physicians and pulmonologists. Cough is an important defensive reflex that enhances the clearance of secretions and particles from the airways and protects the lower airways from the aspiration of foreign materials. Therapeutic suppression of cough may be either disease-specific or symptom related. The potential benefits of an early treatment of cough could include the prevention of the vicious cycle of cough. There has been a long tradition in acute cough, which is frequently due to upper respiratory tract infections, to use symptom-related anti-tussives. Suppression of cough (during chronic cough) may be achieved by disease-specific therapies, but in many patients it is often necessary to use symptomatic anti-tussives, too. According to the current guidelines of the American College of Chest Physician on "Cough Suppressants and Pharmacologic Protussive Therapy" and additional clinical trials on the most frequent anti-tussive drugs, it should be possible to diagnose and treat cough successfully in a majority of cases. Among drugs used for the symptomatic treatment of cough, peripherally acting anti-tussives such as levodropropizine and moguisteine show the highest level of benefit and should be recommended especially in children. By improving our understanding of the specific effects of these anti-tussive agents, the therapeutic use of these drugs may be refined. The present review provides a summary of the most clinically relevant anti-tussive drugs in addition to their potential mechanism of action.Entities:
Year: 2011 PMID: 21985340 PMCID: PMC3205006 DOI: 10.1186/1745-9974-7-7
Source DB: PubMed Journal: Cough ISSN: 1745-9974
Figure 1The acute cough algorithm for the management of patients aged ≥15 years with cough lasting < 3 weeks. PE = pulmonary embolism; Dx = diagnosis; Rx = treatment; URTI = upper respiratory tract infection; LRTI = lower-respiratory tract infection. Taken from Ref [61] with permission from the publisher.
Figure 2Sub acute cough algorithm for the management of patients aged > 15 years with cough lasting 3 to 8 weeks. See the legend of Figure 1 for other section references. Taken from Ref [61] with permission from the publisher.
Figure 3Chronic cough algorithm for the management of cough ≥15 years of age with cough lasting > 8 weeks. ACE-I; ACE-inhibitor; BD = Bronchodilator; LTRA = Leukotrienes receptor antagonist; PPI = Proton Pump Inhibitor. Taken from Ref [61] with permission from the publisher.
Clinical Studies with Codeine
| Study | Sample Size | Design | Disease | Results |
|---|---|---|---|---|
| 81 adults | Not reported | URTI's | Codeine was no more effective | |
| 82 adults | A double-blind, stratified, placebo-controlled, parallel-group, | URTI's | The results demonstrate that codeine is no more effective than placebo in reducing cough associated with acute URTI, as measured by CSPLs, cough frequency or subjective symptom scores |
Clinical Studies with Dextromethorphan
| Study | Sample Size | Design | Disease | Results |
|---|---|---|---|---|
| 44 adults | A double-blind, stratified, randomized and parallel group design | URTI's | This study provides very little if any support for clinically significant antitussive activity of a single 30 mg dose of dextromethorphan in patients with cough associated with URTI's | |
| 451 adults | Review of three different studies randomized, double blind, placebo controlled | URTI's | The results establish the sensitivity and robustness of the cough quantization methodology in the objective evaluation of cough treatments | |
| 710 adults | Six studies used for the meta-analysis were randomized, double-blind, parallel-group, single-dose, placebo-controlled studies with a 3-h postdose cough evaluation period | URTI's | The results of a meta-analysis show that the antitussive effect of a single dose of dextromethorphan hydrobromide, 30 mg, has been established. |
Clinical Studies with Levodropropizine vs Central antitussives in adults
| Study | Sample Size | Design | Disease | Results |
|---|---|---|---|---|
| 174 adults | The studies have been conducted as follow: | Bronchitis | - LDP antitussive action resulted in being higher than placebo and morclofone and similar to cloperastin. | |
| 209 adults | Double blind randomized vs Dextromethorphan | Non productive cough | - The results bear out the effectiveness of LDP as an antitussive comparable with dextromethorphan | |
| 140 adults | Double blind randomized vs Dihydrocodeine | Lung Tumor | - The antitussive effect of LDP was comparable with the reference drug, Dihydrocodeine. LDP induced significantly less somnolence compared to Dihydrocodeine. |
Clinical Studies with Levodropropizine vs Central antitussives in Children
| Study | Sample Size | Design | Disease | Results |
|---|---|---|---|---|
| 254 children aged between | Double blind randomized Dropropizine vs | Non-Productive Cough | There were statistically significant decreases in the frequency of coughing spells and nocturnal awakenings after both LDP and dropropizine treatments with no statistical difference between both group. Somnolence was twice as frequent in the dropropizine group (10.3% vs 5.3%) and the difference is clinically relevant, though not statistically significant. | |
| 77 children aged 2 and 3 years | Double blind randomized LDP vs Dextromethorphan | Bronchitis | The results show the antitussive effectiveness of LDP and point out a more favourable benefit/risk profile when compared with dextromethorphan. | |
| 70 children, age ranged between 2 months and 14 years | Open Label | Respiratory tract disease | - The treatment was effective on 69/70 children. No child showed a worsening in the cough after 24 hours treatment. | |
| 180 children aged between 5 months and 12 years | Open Label | Respiratory tract disease | - The results of the present study prove that the treatment with LDP in children is excellently tolerated and clinically active | |
| 325 children aged between 2 and 14 years | Open label | Non-productive cough | - This study proved the a favourable therapeutic results with limited risk of inefficacy, with the subsequent improvement in the patient's and parents' quality of life, and with remarkably limited risk of intolerance, especially in terms of daytime somnolence. |