Comparative Evaluation of the Loop-Mediated Isothermal Amplification Assay for Detecting Pulmonary Tuberculosis.
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3343/alm.2018.38.2.119
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Chang Ki KIM
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Eun A CHO
			        		
			        		;
		        		
		        		
		        		
			        		Dong Mi SHIN
			        		
			        		;
		        		
		        		
		        		
			        		Sung Won CHOI
			        		
			        		;
		        		
		        		
		        		
			        		So Youn SHIN
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Department of Laboratory Medicine, Hanyang University Guri Hospital, Guri, Korea. psoas95@gmail.com
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Original Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Tuberculosis;
			        		
			        		
			        		
				        		TB-LAMP;
			        		
			        		
			        		
				        		Real-time PCR;
			        		
			        		
			        		
				        		Sensitivity;
			        		
			        		
			        		
				        		Specificity
			        		
			        		
	        			
        			
        		
 
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Acetylcysteine;
				        		
			        		
				        		
					        		Diagnosis;
				        		
			        		
				        		
					        		Methods;
				        		
			        		
				        		
					        		Microscopy;
				        		
			        		
				        		
					        		Nontuberculous Mycobacteria;
				        		
			        		
				        		
					        		Pathology, Molecular;
				        		
			        		
				        		
					        		Real-Time Polymerase Chain Reaction;
				        		
			        		
				        		
					        		Sensitivity and Specificity;
				        		
			        		
				        		
					        		Sputum;
				        		
			        		
				        		
					        		Tuberculosis;
				        		
			        		
				        		
					        		Tuberculosis, Pulmonary*
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:Annals of Laboratory Medicine
	            		
	            		 2018;38(2):119-124
	            	
            	
 
            
            
            	- CountryRepublic of Korea
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	BACKGROUND: Early detection of tuberculosis (TB) is challenging in resource-poor settings because of limited accessibility to molecular diagnostics. The aim of this study was to evaluate the performance of the loop-mediated isothermal amplification kit (TB-LAMP) for TB diagnosis compared with conventional and molecular tests. METHODS: A total of 290 consecutive sputum samples were collected from May till September, 2015. All samples were processed using the N-Acetyl-L-cysteine (NALC) NaOH method and tested by smear microscopy, solid and liquid culture, real-time PCR, and TB-LAMP. RESULTS: The sensitivity of TB-LAMP for smear-positive and smear-negative samples with culture positivity was 92.0% and 58.8%, respectively. TB-LAMP was positive in 14.9% of TB culture-negative samples; however, all those samples were also positive by real-time PCR. In addition, none of the samples positive for nontuberculous mycobacteria by culture were positive by TB-LAMP. The overall agreement between TB-LAMP and real-time PCR was good; however, the concordance rate was significantly lower for real-time PCR positive samples with Ct values of 30–35. CONCLUSIONS: TB-LAMP could replace smear microscopy and increase TB diagnostic capacity when Xpert MTB/RIF is not feasible because of poor infrastructure.