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| Name | Class |
|---|---|
| National Health Laboratory, Myanmar | UNKNOWN |
| Magway General Hospital, Magway | UNKNOWN |
| Monywa Hospital, Sagaing | UNKNOWN |
| Mandalay General Hospital and University of Medicine, Mandalay |
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Rickettsial infections have been found to be the second most common cause of non-malarial febrile illness in Southeast Asia, just after dengue, and are largely neglected treatable causes of morbidity and mortality. The rickettsiae can be divided into three major groups: the scrub typhus group (STG), the typhus group (TG) and the spotted fever group (SFG). Rickettsial infections typically present with an acute fever and are difficult to diagnose due to the many different causes of undifferentiated fever in Southeast Asia. Rickettsial IgG seroprevalence, reflecting past infection, will give an estimate of the burden of rickettsial infections in the population. Background seroprevalence studies in countries around Myanmar have found high rates of rickettsial infections. Yet, in Myanmar there have been no prevalence studies on rickettsial infections since the Second World War. We plan to determine IgG levels to the three different groups of rickettsial infections in leftover blood samples in several clinics and hospitals in different regions of Myanmar.
Rickettsial infections have been found to be the second most common cause of non-malarial febrile illness in Southeast Asia, just after dengue, and are largely neglected treatable causes of morbidity and mortality. The rickettsiae can be divided into three major groups: the scrub typhus group (STG), the typhus group (TG) and the spotted fever group (SFG). Rickettsial infections typically present with an acute fever and are difficult to diagnose due to the many different causes of undifferentiated fever in Southeast Asia. Rickettsial IgG seroprevalence, reflecting past infection, will give an estimate of the burden of rickettsial infections in the population. The current best test for IgG serological diagnosis of previous rickettsial infections is the indirect immunofluorescence assay (IFA). IFA has several limitations
in that it is difficult to standardize due to operator subjectivity, it needs appropriate local diagnostic cut- offs and requires improvement in terms of standardization and ease of use. An alternative serological test that is cheaper and is easier to use is the enzyme-linked immunosorbent assay (ELISA), which is more suited to screen for the burden of rickettsial diseases in low-resource countries. Background seroprevalence studies in countries around Myanmar have found high rates of rickettsial infections. Yet, in Myanmar there have been no prevalence studies on rickettsial infections since the Second World War. We plan to determine IgG levels to the three different groups of rickettsial infections in leftover blood samples in several clinics and hospitals in different regions of Myanmar. Participants with leftover blood samples after having undergone a blood draw for any clinical reason or a blood donation will be requested to participate in the study. The participant will be informed about the study and requested to provide informed consent when agreeing to participate. The leftover sample will be anonymized and frozen. The gender, age and location of clinic/hospital of the participant will be recorded. All samples will be tested for IgG antibodies using an in-house ELISA test in the Mahidol Oxford Tropical Medicine Research Unit (MORU), Bangkok, Thailand for scrub typhus (Orientia tsutsugamushi strains Karp, Kato, Gilliam and TA716), murine typhus (Rickettsia typhi strain type Wilmington), and spotted fever rickettsioses (Rickettsia honei and Rickettsia conorii). If the sample tests positive for IgG antibodies, an IFA test will be performed as the gold standard reference test to confirm the finding. The anonymous samples will be discarded as soon as they are no longer needed for the study. The population investigated will be 700 patients attending seven different clinics and hospitals in different regions of Myanmar with each site including 100 patients.
We will include patients at the following study sites:
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MORU in-house ELISA test followed by IFA if positive | Diagnostic Test | An in-house rickettsial IgG ELISA test will be used for this study to determine previous rickettsial infections by measuring IgG levels. All specimens will be tested for IgG antibodies using ELISA tests for scrub typhus (Orientia tsutsugamushi strains Karp, Kato, Gilliam and TA716), murine typhus (Rickettsia typhi strain type Wilmington), and spotted fever rickettsiosis (Rickettsia honei and Rickettsia conorii). If the sample tests positive, it will be retested for the same antigens using the IFA test. The sample will be considered positive if both the ELISA and the IFA are positive. |
| Measure | Description | Time Frame |
|---|---|---|
| Positive ELISA confirmed by positive IFA | Proportion of patients with a positive IgG ELISA, subsequently confirmed with IFA, for scrub typhus (Orientia tsutsugamushi strains Karp, Kato, Gilliam and TA716), murine typhus (Rickettsia typhi strain type Wilmington), and spotted fever rickettsiosis (Rickettsia honei and Ricketsia conorii). | January, 2020 |
| Measure | Description | Time Frame |
|---|---|---|
| Patient characteristics associated with rickettsial infections | Correlation of different patient characteristics with a positive ELISA and IFA test indicating a previous rickettsial infection. | January, 2020 |
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Inclusion Criteria:
Exclusion Criteria:
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The population investigated will be patients who had a leftover samples from routine clinical blood draw when attending seven different Medical Action Myanmar (MAM) clinics and hospitals in different regions of Myanmar with each site including approximately 100 patients.
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| Name | Affiliation | Role |
|---|---|---|
| Elizabeth Anne Ashley, Dr | Myanmar Oxford Clinical Research Unit | Principal Investigator |
| Stuart Blacksell, Prof | Mahidol Oxford Tropical Medicine Research Unit | Principal Investigator |
| Philip Elders, MSc | Myanmar Oxford Clinical Research Unit | Study Director |
| Wei Yan Aung Htay, Dr | Myanmar Oxford Clinical Research Unit | Study Director |
| Yin Yin Htwe, Dr | National Health Laboratory, Myanmar | Study Director |
| Myat Myat Moe, Dr | Magway General Hospital, Magway | Study Director |
| Wai Mon Kyaw, Dr | Monywa Hospital, Sagaing | Study Director |
| Ni Ni Zaw, Dr | Mandalay General Hospital and University of Medicine, Mandalay | Study Director |
| Win May Thein, Prof | Mandalay General Hospital and University of Medicine, Mandalay | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Myanmar Oxford Clinical Research Unit | Yangon | Burma |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22970193 | Background | Acestor N, Cooksey R, Newton PN, Menard D, Guerin PJ, Nakagawa J, Christophel E, Gonzalez IJ, Bell D. Mapping the aetiology of non-malarial febrile illness in Southeast Asia through a systematic review--terra incognita impairing treatment policies. PLoS One. 2012;7(9):e44269. doi: 10.1371/journal.pone.0044269. Epub 2012 Sep 6. | |
| 24957537 |
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| UNKNOWN |
| University of Medicine, Magway | UNKNOWN |
| Mahidol Oxford Tropical Medicine Research Unit | OTHER |
| Medical Action Myanmar | OTHER |
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| Thin Thin Nwe, Prof | University of Medicine, Magway | Study Director |
| Kyaw Soe, BSc | Myanmar Oxford Clinical Research Unit | Study Director |
| Ampai Tanganuchitcharnchai, BSc | Mahidol Oxford Tropical Medicine Research Unit | Study Director |
| Ni Ni Tun, Dr | Myanmar Oxford Clinical Research Unit and Medical Action Myanmar | Study Director |
| Frank Smithuis, Prof | Myanmar Oxford Clinical Research Unit and Medical Action Myanmar | Study Director |
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