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Volume 15, Number 11—November 2009

Screening Practices for Infectious Diseases among Burmese Refugees in Australia

Nadia J. Chaves1, Katherine B. Gibney1, Karin Leder, Daniel P. O’Brien, Caroline Marshall, and Beverley-Ann BiggsComments to Author 
Author affiliations: Royal Melbourne Hospital, Parkville, Victoria, Australia (N.J. Chaves, K.B. Gibney, K. Leder, D.P. O’Brien, C. Marshall, B.-A. Biggs); Monash University, Melbourne, Victoria, Australia (K. Leder); Médecins sans Frontières Holland, Amsterdam, the Netherlands (D.P. O’Brien); University of Melbourne, Parkville (C. Marshall, B.-A. Biggs); 1These authors contributed equally to this article.

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Increasing numbers of refugees from Burma (Myanmar) are resettling in Western countries. We performed a retrospective study of 156 Burmese refugees at an Australian teaching hospital. Of those tested, Helicobacter pylori infection affected 80%, latent tuberculosis 70%, vitamin D deficiency 37%, and strongyloidiasis 26%. Treating these diseases can prevent long-term illness.

Burma (Myanmar) has been the most common country of origin for refugees who have recently resettled in the United States and Australia (1,2). Before resettling in Australia, most refugees undergo testing for HIV, have a chest radiograph to exclude active tuberculosis (TB), and may undergo other testing, depending on exposure risk. Many refugees also receive a health check and treatment for malaria and stool parasites within 72 hours of departure for Australia (3,4). Most refugees who resettle in Victoria, Australia, are screened by primary care doctors and then referred to specialist clinics as appropriate. In this study, we examined the effect of illness and the adequacy and completeness of health screening among Burmese refugees referred to the infectious diseases clinic of an Australian tertiary hospital during a 5-year period.


We performed a retrospective cohort study of all Burmese refugees who attended the Victorian Infectious Diseases Service outpatient clinics at the Royal Melbourne Hospital, Australia, during January 1, 2004–December 31, 2008. Patients were identified through the hospital registration database, and medical, pathologic, radiologic, and pharmacologic records were reviewed. Screening tests audited included those suggested by the Australasian Society for Infectious Diseases refugee screening guidelines (5), along with vitamin D and hematologic studies. These latter tests included full blood count, mean corpuscular volume, and platelet count. Investigations were performed at the discretion of the treating doctor, and not all tests were performed for each patient. Time was calculated from time of arrival in Australia to first clinic attendance. The results of serologic tests and QuantiFERON-TB Gold tests (QFT-G; Cellestis Limited, Carnegie, Victoria, Australia), were interpreted according to the manufacturers’ recommendations.

Conditions were defined according to prespecified criteria as follows: schistosomiasis; strongyloidiasis; HIV and syphilis (positive serologic test results); hepatitis C virus (RNA detected by PCR); Helicobacter pylori (positive results for fecal antigen test, carbon-14 breath test, or serologic analysis); malaria (thick and thin blood films or immunochromatographic test result positive for Plasmodium species); chlamydia and gonorrhea (DNA detected by PCR in first-pass urine); active TB (microbiologic or histologic evidence of Mycobacterium tuberculosis infection or receiving treatment for active TB during the study period); latent TB infection (Mantoux test result >10 mm or positive QFT-G result and no clinical evidence of active disease); chronic hepatitis B virus (HBV; hepatitis B surface antigen detected); isolated core antibody against HBV (hepatitis B core antibody detected, hepatitis B surface antibody and hepatitis B surface antigen not detected); pathologic stool parasites (stool microscopy positive for a pathogenic species); vitamin D deficiency (serum 25[OH] vitamin D level <50 nmol/L); anemia (hemoglobin level <120g/L); and eosinophilia (eosinophil count >0.4 × 109 cells/L). The Melbourne Health Human Research Ethics Committee approved this study as a quality assurance audit.



Thumbnail of Proportion of 156 recently arrived Burmese refugees with documented screening tests for common health conditions, Australia, 2004–2008. Most of these tests are recommended by the Australasian Infectious Diseases Society guidelines (5). Tests for vitamin D levels are beyond the scope of these guidelines. Black, tested; red, not tested.

Figure. Proportion of 156 recently arrived Burmese refugees with documented screening tests for common health conditions, Australia, 2004–2008. Most of these tests are recommended by the Australasian Infectious Diseases Society guidelines (<>

A total of 156 Burmese refugees were referred to the infectious diseases outpatient clinics at the Royal Melbourne Hospital during the study period. Table 1 summarizes the characteristics of these patients. Median age was 30 years (range 16–86 years); approximately half were male (51%) and of Karen ethnicity (48%). Most refugees were born in Burma (97%) and had spent time in a refugee camp (97%). The proportion of these patients who were screened according to the Australian refugee health guidelines is shown in the Figure. More than 90% of study patients were tested for 6 diseases (Mycobacterium TB, HIV, hepatitis B, hepatitis C, schistosomiasis, and Strongyloides stercoralis infection).

Table 2 shows the prevalence of selected medical conditions in this patient group. Chronic HBV infection was found in 14% of the group; isolated core antibody against HBV was found in 13%. Hepatitis B DNA was not detected in the serum of any patients with isolated core antibody against HBV. One person had HIV infection; this person had a chronic infection with HBV. H. pylori infection was identified in 80% of those tested (7 persons by carbon-14 breath test, 7 by fecal antigen test, and 19 by serologic analysis). No cases of multidrug-resistant TB were found.

Eosinophilia was documented in 35% of those tested, 47% of whom had strongyloidiasis, 4% schistosomiasis, and 24% a pathologic stool parasite that causes eosinophilia. Eosinophilia was not explained by these conditions in 33%.


In recent years, an increasing number of refugees from Burma have resettled in Australia, North America, and Europe. This study reports high rates of H. pylori infection (80%), latent TB infection (70%), vitamin D deficiency (37%), and strongyloidiasis (26%) in Burmese refugees attending the infectious diseases clinics of a Melbourne tertiary referral hospital.

A Canadian study of 68 Karen refugees, more than half of whom were <18 years of age, appears to be the only previously published study on the health status of Burmese refugees settled in a Western country (6). One unpublished study found on the Internet was conducted by the Minnesota Department of Health, which examined 159 Burmese migrants, but no demographic information was included (7). We have compared our screening results with those of these 2 studies in Table 2.

A high rate of parasitic intestinal infections has been documented in refugees from Burma in Thailand (810) and North America (6,7), and our findings are consistent with these studies. Parasitic intestinal infections were common in our study despite some refugees reporting that they had received predeparture drug therapy with albendazole. Therefore, we suggest that refugees migrating from Burma to Australia who underwent postarrival stool evaluation may not have received the predeparture antiparasitic, or if received, the treatment was ineffective. Moreover, infection with S. stercoralis was common in this study. This parasite is unlikely to be eradicated with only 1 dose of albendazole and is associated with chronic complications, including hyperinfection syndrome and death (11).

The rate of infection with H. pylori in this group was surprisingly high at 80% because the number of refugees tested was small and those tested were symptomatic. High rates of infection with H. pylori have been seen in other immigrant groups (12,13). This result reinforces the need to question refugees regarding dyspeptic symptoms and to test those with symptoms because of established links between H. pylori infection and iron deficiency, peptic ulcer disease, and gastric cancer (14,15).

National screening protocols for refugees were closely followed in this study for most infectious diseases. Lower compliance (<88%) with screening protocols was reported for malaria, chlamydia, and gonorrhea. However, these conditions were uncommon in this group. Ongoing education of health professionals who care for refugees is required to encourage more complete screening of refugees.

This study has a number of limitations. A relatively small number of patients were tested. Because this study was retrospective and screening was incomplete for some patients, certain diseases may be underestimated, or if testing was based on symptoms rather than true screening, diseases may be overestimated. Some conditions will be overrepresented because of referral bias and because certain tests (e.g., for H. pylori) were performed as diagnostic evaluation of symptomatic patients. This study highlights the difficulties in providing complete health screening for refugees, outlines the range of health problems among Burmese refugees referred to an adult tertiary hospital in Australia, and reinforces the high prevalence of treatable conditions in refugee communities.

Dr Chaves is an infectious diseases fellow at the Victorian Infectious Diseases Service at the Royal Melbourne hospital in Melbourne. Her primary research interests are immigrant and refugee health and travel medicine.



We thank Ashleigh Carr and Libby Matchett for assistance with medical record collection and database management and Chris Lemoh and other staff of the Immigrant and Travel Clinic at Royal Melbourne Hospital for critical review of the manuscript.



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DOI: 10.3201/eid1511.090777

Table of Contents – Volume 15, Number 11—November 2009

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Please use the form below to submit correspondence to the authors or contact them at the following address:

Beverley-Ann Biggs, Department of Medicine (RMH/WH), The University of Melbourne, 4th Floor, Clinical Sciences Bldg, The Royal Melbourne Hospital, Parkville, Victoria 3050, Australia

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