Login to your account

Username *
Password *
Remember Me

Blog With Right Sidebar

Comparison of molecular and immunological methods for the rapid diagnosis of smear-negative tuberculosis.

Related Articles

Comparison of molecular and immunological methods for the rapid diagnosis of smear-negative tuberculosis.

Int J Tuberc Lung Dis. 2013 Nov;17(11):1459-65

Authors: Jafari C, Ernst M, Kalsdorf B, Lange C

Abstract
SETTING: The rapid diagnosis of pulmonary tuberculosis (TB) can be challenging if acid-fast bacilli are not detected by sputum smear microscopy.
OBJECTIVE: To compare the results of the GeneXpert® MTB/RIF assay on a single sputum or bronchoalveolar lavage (BAL) specimen test with local immunodiagnosis from the site of disease using the T-SPOT®.TB assay on BAL (BAL T-SPOT).
DESIGN: The Xpert and BAL T-SPOT tests were compared in 96 patients suspected of having sputum smear-negative pulmonary TB admitted to a referral centre in Germany.
RESULTS: BAL T-SPOT identified 10 of 11 patients with pulmonary TB (including 3/4 patients with culture-confirmed TB) with a negative Xpert test. Using Xpert, the sensitivity, specificity and positive and negative likelihood ratios (LRs) were respectively 60.0%, 97.4%, 30.0% and 0.4% in culture-confirmed cases and 42.1%, 97.4%, 21.1% and 0.6% in all TB patients. In contrast, using BAL T-SPOT, the sensitivity, specificity and positive and negative LRs were respectively 80.0%, 62.6%, 2.1% and 0.3% in culture-confirmed cases and 89.4%, 62.6%, 2.4% and 0.2% in all TB patients.
CONCLUSION: In sputum smear-negative TB suspects, a positive Xpert result is strongly indicative of culture confirmation; however, a negative result is insufficient to rule out active TB. Where clinical suspicion of pulmonary TB persists despite a negative Xpert result, local immunodiagnosis using T-SPOT on BAL may increase diagnostic accuracy.

PMID: 24125451 [PubMed - in process]

Update in tuberculosis and nontuberculous mycobacterial disease 2012.

Related Articles

Update in tuberculosis and nontuberculous mycobacterial disease 2012.

Am J Respir Crit Care Med. 2013 Oct 15;188(8):923-7

Authors: Menzies D, Nahid P

Abstract
In 2012, new publications in the Journal described both the predictive value of the new IFN-γ release assays for diagnosis of latent tuberculosis (TB), but also provided evidence that these new tests cannot be interpreted simply as positive or negative, as initially hoped. Surgical masks can reduce transmission of TB infection, but other measures such as state-wide implementation of targeted testing and treatment of latent TB or active case finding require substantial and sustained effort to successfully reduce TB morbidity and mortality. A quasiexperimental study revealed that a package of social interventions could substantially reduce risk of TB disease in heavily exposed (and infected) children in the preantibiotic era. A study in a high-TB burden setting suggested that a new rapid drug-susceptibility test for TB may be more practical for implementation than traditional culture-based phenotypic tests. And two studies of TB vaccines revealed that currently used bacillus Calmette-Guérin strains vary in their ability to affect correlates of immunogenicity, whereas a new candidate vaccine, MVA85A, was safe and immunogenic in adults. Studies of nontuberculous mycobacteria (NTM) described a rapid rise in the prevalence and spatial clustering of NTM in the United States over the past decade. Although risk factors for pulmonary NTM such as advanced age and low BMI are known, the mechanisms underlying infection and disease remain mysterious. Four studies of therapy of NTM disease highlighted the pressing need for well-designed international randomized controlled trials to improve our management of NTM disease.

PMID: 24127799 [PubMed - in process]

South African tobacco smoking cessation clinical practice guideline.

Related Articles

South African tobacco smoking cessation clinical practice guideline.

S Afr Med J. 2013 Nov;103(11):869-76

Authors: Van Zyl-Smit RN, Allwood B, Stickells D, Symons G, Abdool-Gaffar S, Murphy K, Lalloo U, Vanker A, Dheda K, Richards G

Abstract
Tobacco smoking (i.e. cigarettes, rolled tobacco, pipes, etc.) is associated with significant health risks, reduced life expectancy and negative personal and societal economic impact. Smokers have an increased risk of cancer (i.e. lung, throat, bladder), chronic obstructive pulmonary disease (COPD), tuberculosis and cardiovascular disease (i.e. stroke, heart attack). Smoking affects unborn babies, children and others exposed to second hand smoke. Stopping or 'quitting' is not easy. Nicotine is highly addictive and smoking is frequently associated with social activities (e.g. drinking, eating) or psychological factors (e.g. work pressure, concerns about body weight, anxiety or depressed mood). The benefits of quitting, however, are almost immediate, with a rapid lowering of blood pressure and heart rate, improved taste and smell, and a longer-term reduction in risk of cancer, heart attack and COPD. Successful quitting requires attention to both the factors surrounding why an individual smokes (e.g. stress, depression, habit, etc.) and the symptoms associated with nicotine withdrawal. Many smokers are not ready or willing to quit and require frequent motivational input outlining the benefits that would accrue. In addition to an evaluation of nicotine dependence, co-existent medical or psychiatric conditions and barriers to quitting should be identified. A tailored approach encompassing psychological and social support, in addition to appropriate medication to reduce nicotine withdrawal, is likely to provide the best chance of success. Relapse is not uncommon and reasons for failure should be addressed in a positive manner and further attempts initiated when the individual is ready.Key steps in smoking cessation include: (i) identifying all smokers, alerting them to the harms of smoking and benefits of quitting; (ii) assessing readiness to initiate an attempt to quit; (iii) assessing the physical and psychological dependence to nicotine and smoking; (iv) determining the best combination of counselling/support and pharmacological therapy; (v) setting a quit date and provide suitable resources and support; (vi) frequent follow-up as often as possible via text/telephone or in person; (vii) monitoring for side-effects, relapse and on-going cessation; and (viii) if relapse occurs, providing the necessary support and encourage a further attempt when appropriate. 

PMID: 24148176 [PubMed - in process]

Corticosteroids for prevention of tuberculosis mortality.

Related Articles

Corticosteroids for prevention of tuberculosis mortality.

Lancet Infect Dis. 2013 Nov;13(11):915

Authors: Madan K, Yadav SS, Wig N, Guleria R

PMID: 24156890 [PubMed - in process]

Serial lobar lung lavage in pulmonary alveolar proteinosis.

Related Articles

Serial lobar lung lavage in pulmonary alveolar proteinosis.

J Bronchology Interv Pulmonol. 2013 Oct;20(4):333-7

Authors: Baldi MM, Nair J, Athavale A, Gavali V, Sarkar M, Divate S, Shah U

Abstract
Pulmonary alveolar proteinosis (PAP) is a rare disease with worldwide distribution and an estimated incidence of 0.36 cases per million. We report a case of a PAP coexisting with Pneumocystis jiroveci pneumonia and Mycobacterium tuberculosis infection. The patient was treated with serial lobar lung lavages, GM-CSF, cotrimoxazole, and antituberculosis drugs. His PaO2 on room air improved from 45.7 to 63.8 torr and pulmonary functions normalized (FVC 81.2%, FEV1 95.3%, FEV1/FVC 91.8). A high-resolution computed tomography scan of the thorax showed clearing of both lower lobes. Whole-lung lavage is used in the treatment of PAP, but it may worsen the hypoxemia and lead to hemodynamic instability during the procedure. To the best of our knowledge, there are no reports of bronchoscopic serial lobar lung lavages in cases of PAP performed in India. This method can be performed in bronchoscopic suites having general anesthesia facilities without the requirement of special gadgets.

PMID: 24162118 [PubMed - in process]

Search