Trial of Amoxicillin Compared With Placebo for Pneumonia in Children Aged 2-59 Months

Pneumonia Clinical Trial

Official title: A Randomized Multicentre Double Blind Trial of Amoxicillin Compared With Placebo for Treatment of WHO Defined Non-Severe Pneumonia in Children Aged 2-59 Months: NARIMA Study Group

Status Completed

Clinical Trial Summary

Many children with "non-severe pneumonia" (cough and fast breathing) have neither clinical pneumonia as assessed by physicians nor pneumonia on chest radiographs. Inappropriate use of antibiotics for these cases is leading to resistant strains of bacteria in the community. Evidence shows that almost 50% of antibiotic prescription is unnecessary.As over half of antibiotic prescription for ARI are not necessary since most of these infections are viral and do not respond to antibiotic therapy which will be source of resistance in the community.

To address this issue the investigators conducted this randomized, double blind placebo controlled clinical trial of oral Amoxicillin versus placebo in children with non-severe pneumonia taking into account all the necessary safety precautions for their well being.

The study hypothesis was that the clinical outcome of children 2 to 59 months of age with cough and fast breathing (WHO defined non-severe pneumonia) with or without wheezing is equivalent, whether they are treated with amoxicillin or placebo.

Clinical Trial Description

Pneumonia is one of the major cause of childhood morbidity and mortality in developing countries. Burden of acute respiratory infections (ARI) is high with an estimated 5-7 episodes in under 5 population every year resulting in 2 million deaths. However, most of these are due to severe bacterial pneumonia.

In order to reduce pneumonia related deaths in communities where qualified personnel and diagnostic facilities are often not available WHO developed management guidelines based on simple clinical signs followed by empirical treatment. All children with cough and fast breathing are classified into management categories: Children with fast breathing only are classified as having non-severe pneumonia requiring oral antibiotic at home, children who have lower chest indrawing and /or general danger signs (GDS) are classified as severe pneumonia, and very severe pneumonia respectively. Both these groups require referral to a hospital and injectible antibiotic therapy. These guidelines have shown to effectively reduce ARI related mortality by 34% (?) in communities where they have been successfully implemented.

However, there are certain concerns regarding these guidelines. It is felt that using the sign of fast breathing alone for prescribing antibiotic may not be the most judicious thing from a public health perspective as it may lead to the spread of antibiotic resistance. Fast breathing could be due to many other causes not related to pneumonia.

There are many factors affecting the respiratory rate I children. Children with fever will have elevated respiratory rates in any case. Although WHO guidelines recommend that respiratory rate must be counted when child is afebrile, calm and preferably sleeping. In real life such practice is not always possible.

Another issue is the children with cough and fast breathing who have wheezing. In many developing countries wheeze is commonly associated with fast and difficult breathing. Data from the developed countries shows that wheeze is more common in viral than bacterial infections. Likewise, data from the developing countries has shown that viruses, especially respiratory syncytial virus (RSV), are isolated more frequently than bacteria from children with episodes of acute lower respiratory tract infections. A randomized trial of infants with bronchiolitis and pneumonia found no difference in clinical outcome in children with antibiotics compared with placebo(ref?). Wheeze has long been unaddressed and is one of the major cause for overuse of antibiotics. Evidence shows that three cycles of inhaled bronchodilator was found to be associated with a significant decrease in respiratory rate leading to revised classification of "no pneumonia" in these children. It has convincingly shown that majority of these children continue to do well when sent home without an antibiotic.

Though fast breathing is an important indicator for clinical diagnosis of pneumonia it cannot distinguish viral from bacterial pathogens Controversy still exists concerning the relative importance of viral and bacterial pathogens so a reliable distinction between bacterial and viral infection has yet to be established and this issue has raised a lot of questions for the programme managers, senior researchers and technical experts, which still need to be answered.

Many children with "non-severe pneumonia" (cough and fast breathing) have neither clinical pneumonia as assessed by physicians nor pneumonia on chest radiographs. Inappropriate use of antibiotics for these cases is leading to resistant strains of bacteria in the community. Evidence shows that almost 50% of antibiotic prescription is unnecessary. As over half of antibiotic prescription for ARI are not necessary since most of these infections are viral and do not respond to antibiotic therapy which will be source of resistance in the community. When resistant bacteria become common, we may begin to see treatment failures in the children with severe pneumonia who really require an effective antibiotic. It is imperative to have the knowledge of likely cause and pattern of pneumonia which could be utilized to better understand the model of antibiotic resistance.

For the above stated reasons, there is a need to further elaborate the role of antibiotics in children with cough and fast breathing. To address this issue we conducted this randomized, double blind placebo controlled clinical trial of oral Amoxicillin versus placebo in children with non-severe pneumonia taking into account all the necessary safety precautions for their well being. The primary objective was to determine whether children aged 2 to 59 months with cough and fast breathing, with or without wheezing, but no evidence of WHO defined severe illness, have equivalent clinical failure at 72 hours of therapy when treated with Amoxicillin compared to placebo. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Acute Respiratory Infections
• Pneumonia
• Respiratory Tract Infections

• NCT number: NCT00851487
• Study type: Interventional
• Source: Pakistan Institute of Medical Sciences
• Status: Completed
• Phase: N/A
• Start date: January 2006
• Completion date: April 2008