Causes of Pneumonia in Yangon

January 9, 2020 updated by: Myanmar Oxford Clinical Research Unit

A Cross-sectional Study Investigating the Causes of Pneumonia in Two Community Clinics in Two Yangon Townships, Myanmar

This study will evaluate a new point of care diagnostic test for the diagnosis of melioidosis pneumonia in patients attending outpatient clinics in Yangon, Myanmar

Study Overview

Detailed Description

Melioidosis is caused by Burkholderia pseudomallei, a Gram-negative saprophytic environmental bacterium that is an important emerging tropical infection. There are an estimated 165,000 cases and 89,000 deaths world-wide each year. Eighty-four percent of cases are in SE Asia where mortality is 40%; far exceeding most recognised neglected tropical diseases. Pneumonia, secondary to either inhalation of B.pseudomallei or to bacteraemic spread to the lung is the commonest presentation (51%). Annually the highest burden (75%) of infection occurs in the rainy season in (75% in Thailand). Up to 80% patients have at least one recognised risk factor for melioidosis including; diabetes, alcohol-dependence, glucocorticoid therapy, chronic obstructive pulmonary disease (COPD), chronic renal disease and cancer. COPD and diabetes mellitus are amongst the top ten causes of death in Myanmar (2018). Patients with HIV have not been shown to have greater risk of B. pseudomallei than immunocompetent patients.

Melioidosis was discovered in Myanmar in 1911 by British pathologist Alfred Whitmore and his assistant CS Krishnaswami. Yet since 1949 there have been few published cases. Under-reporting is partly due to difficulty in diagnosing melioidosis. Clinical and radiological findings are indistinguishable from tuberculosis. Laboratory diagnosis is challenging, lack of facilities, expertise and awareness of B.pseudomallei results in missed diagnostic opportunities.

Culture is the gold-standard diagnostic method but requires appropriate facilities and expertise which are not readily available in many developing countries like Myanmar. A rapid diagnostic (RDT) test has been developed for low resource settings that has been evaluated in Laos and India. The InBios® Active Melioidosis DetectTM-Lateral Flow Assay (AMD-LFA) detects B.pseudomallei 6-deoxyheptan capsular polysaccharide antigen. Shaw et al demonstrated sensitivity 85.71% (CI:74.61% to 93.25%) and specificity 93.62% (CI:88.23% to 97.04%), with positive predictive value of 85.71% (CI: 75.98% to 91.92%) compared to culture. We propose to evaluate this test for the diagnosis of melioidosis pneumonia in Myanmar.

Study Type

Observational

Enrollment (Actual)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Yangon, Myanmar
        • Medical Action Myanmar Clinics

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

The population investigated will be patients attending two non-governmental organisation community clinics in the most deprived areas of Yangon, Myanmar

Description

Inclusion Criteria:

  1. >18 years old
  2. Reported fever or axillary temperature > 37.5 °C
  3. Productive cough
  4. Written informed consent

Exclusion Criteria:

1. Inability to provide a sputum specimen

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of patients with a positive B.pseudomallei culture result
Time Frame: January 2019
Number of patients with a positive sputum culture for B.pseudomallei expressed as a proportion of all patients
January 2019
1) Sensitivity, specificity, positive predictive value, negative predictive value of the RDT compared to culture
Time Frame: January 2019
Using culture as the gold-standard the performance of the lateral flow assay will be assessed
January 2019

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of patients diagnosed with tuberculosis (TB) including multidrug resistant TB
Time Frame: January 2019
Proportion of enrolled participants with a positive GeneXpert MTB/RIF test on sputum
January 2019
Proportion of patients diagnosed with Influenza A/B
Time Frame: March 2019
Proportion of enrolled participants with a positive Xpert Flu test on nasopharyngeal swab
March 2019

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Elizabeth A Ashley, Dr, Myanmar Oxford Clinical Research Unit
  • Study Director: Clare Warrell, Dr, Myanmar Oxford Clinical Research Unit and Medical Action Myanmar
  • Study Director: David Dance, Prof, Lao-Oxford-Mahosot Hospital Wellcome Trust Research Unit
  • Study Director: Mo Mo Win, Dr, Department of Medical Research, Myanmar
  • Study Director: Alistair McLean, Dr, Myanmar Oxford Clinical Research Unit

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

July 9, 2018

Primary Completion (ACTUAL)

April 4, 2019

Study Completion (ACTUAL)

April 4, 2019

Study Registration Dates

First Submitted

June 24, 2018

First Submitted That Met QC Criteria

June 24, 2018

First Posted (ACTUAL)

July 5, 2018

Study Record Updates

Last Update Posted (ACTUAL)

January 13, 2020

Last Update Submitted That Met QC Criteria

January 9, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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