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1.
Int J Tuberc Lung Dis ; 19(5): 545-51, 2015 May.
Article in English | MEDLINE | ID: mdl-25868022

ABSTRACT

SETTING: The Xpert(®) MTB/RIF assay is a highly sensitive molecular test with the potential to improve tuberculosis (TB) case detection. However, evidence supporting this potential at a programme level is minimal. METHODS: Xpert testing following smear microscopy and chest X-ray was implemented as part of routine case finding in 16 districts of Eastern Nepal. Changes in TB case notification were evaluated based on a pre/post analysis, as were expected notifications based on linear trend. RESULTS: A total of 9723 Xpert tests were performed, resulting in the identification of 1662 Mycobacterium tuberculosis-positive patients. Despite a previous declining trend in notifications, annual bacteriologically positive TB notifications increased by 15.2% during the intervention, from 3390 to 3906. However, annual notifications of pulmonary TB dropped by 8.5% overall, from 5123 to 4688. Both observations were significantly different from expected notifications based on historical trends. Treatment initiation for drug-resistant TB almost doubled. DISCUSSION: Xpert testing significantly increased bacteriologically positive TB notifications, but large reductions in empiric treatment of smear-negative disease reduced the number of pulmonary TB notifications overall. While better diagnostics remain critical, focusing solely on superior test sensitivity may not increase TB case notifications. Additional interventions are required to reach the millions of people with TB who are missed by routine services.


Subject(s)
Antitubercular Agents/administration & dosage , Communicable Disease Control/organization & administration , Disease Notification/statistics & numerical data , Molecular Diagnostic Techniques/methods , Tuberculosis, Pulmonary/diagnosis , Adolescent , Antitubercular Agents/pharmacology , Child , Child, Preschool , Confidence Intervals , DNA, Bacterial/analysis , Disease Notification/methods , Female , Humans , Male , Nepal/epidemiology , Polymerase Chain Reaction/methods , Quality Improvement , Radiography, Thoracic/methods , Sensitivity and Specificity , Sputum/microbiology , Tuberculosis, Multidrug-Resistant/diagnosis , Tuberculosis, Multidrug-Resistant/drug therapy , Tuberculosis, Pulmonary/drug therapy , Tuberculosis, Pulmonary/epidemiology , Young Adult
2.
Kathmandu Univ Med J (KUMJ) ; 11(41): 14-7, 2013.
Article in English | MEDLINE | ID: mdl-23774406

ABSTRACT

BACKGROUND: Visceral leishmaniasis is potentially fatal protozoan diseases caused by Leishmania donovani. Nepal is an endemic region in which visceral leishmaniasis causes a major public health problem in the lowland areas that border the endemic areas of Bihar state in India. Accurate diagnosis to inform treatment is a first step in achieving the goal of visceral leishmaniasis elimination from South East Asian regions by 2020. OBJECTIVE: The objective of the present study was to compare between the Microcopy and polymerase chain reaction for diagnosis of visceral leishmaniasis. METHODS: In the present study, 236 bone marrow aspirations were collected from suspected visceral leishmaniasis patients in Janakpur Zonal Hospital, Dhanusa district, Terai region of Nepal in between 2003-2007. We evaluated bone marrow samples by microscopic examination with subsequent testing of the same sample by polymerase chain reaction and sequence analysis. RESULTS: Giemsa's solution stained bone marrow slides stored for over five years were used for polymerase chain reaction amplification. The result showed that 71% were polymerase chain reaction positive and 56% were microscopic positive. Out of 104 microscopic negative bone marrow samples, 15% of samples were positive by polymerase chain reaction. CONCLUSION: Polymerase chain reaction could make a very good option for diagnosis by using less or non-invasive material from visceral leishmaniasis patients in endemic areas of Nepal.


Subject(s)
Bone Marrow/pathology , DNA, Protozoan/analysis , Leishmania donovani/genetics , Leishmaniasis, Visceral/diagnosis , Polymerase Chain Reaction/methods , Adolescent , Adult , Animals , Biopsy, Needle , Bone Marrow/parasitology , Diagnosis, Differential , Female , Humans , Leishmaniasis, Visceral/genetics , Leishmaniasis, Visceral/parasitology , Male , Middle Aged , Reproducibility of Results , Retrospective Studies , Young Adult
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