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Denny John Prabir Chatterjee Shruti Murthy Ramesh Bhat Baba Maiyaki Musa 《The Indian journal of tuberculosis》2018,65(3):208-217
Background
In India, multidrug-resistant tuberculosis (MDR-TB) patients are usually treated in hospitals. Decentralised care model, however, has been suggested as a possible alternative by the World Health Organization (WHO). In the “End TB Strategy”, the WHO highlights, as one of the key targets for 2035, that ‘no TB-affected families should face catastrophic hardship due to the tuberculosis’. Removal of financial barriers to health-care access and mitigation of catastrophic expenditures are therefore considered vital to achieve the universal health coverage (UHC) goal. Since forgoing healthcare due to the financial constraints is a known fact in India, decentralised care as an intervention choice (as against hospital-based care) might enhance equity provided it is an affordable choice. Thus, an economic evaluation was conducted, from the perspective of the national health system in India, to assess the cost-effectiveness of decentralised care compared to centralised care for MDR-TB.Methods
This study uses a decision-analytic model with a follow-up of two years to assess the expected costs of the decentralised versus the centralised approaches for MDR-TB treatment. A published systematic review of observational studies yielded the MDR-TB treatment outcomes, which included treatment success, treatment default, treatment failure, and mortality parameters. It was observed that these parameters did not vary significantly between the two alternatives. Treatment costs included the following costs: hospital admission costs, clinic costs, visits to laboratory and MDR-TB centre, drug therapy, injections and food. Costs data of drugs, diagnosis, hospital stay and travel to public facilities, based on a simple market survey, were taken from a recently published study on MDR-TB expenditures in the Chhattisgarh state of India. Potential cost savings related to the implementation of decentralised MDR-TB care for all patients who initiated MDR-TB treatment in India were additionally estimated.Results
Estimated average expected total treatment cost was US$ 3390.56 for the hospital-based model and US$ 1724.1 for the decentralised model for a patient treated for MDR-TB in India, generating potential savings of US$1666.50 per case, with ICER US$ 2382.68 per QALY gained. One of the primary drivers of this difference was the significantly more intensive (thus expensive) stay charges in the hospital. If the costs and treatment probabilities are extrapolated to the whole country, with 48114 MDR-TB patients initiated on treatment in 2017, decentralised care would have additional 1058 patients cured, gain additional 3824 QALYs, and avert 2165 deaths, as compared to centralised care, in India. At various scenarios of coverage rates of decentralised and centralised care the cost difference would range between 23% and 94% for the country.Conclusion
Our study provides evidence of cost savings for MDR-TB patients if patients choose decentralised treatment in comparison to suggested hospitalisation of these patients for centralised treatment with similar outcomes. The economic evaluation presented in this study expected significant efficiency gains in choice of two treatment options and the cost savings may improve equity. In India, treatment of MDR-TB using decentralised care is expected to result in similar patient outcomes at markedly reduced public health costs compared with centralised care. 相似文献4.
Amit Kumar Sharma Neeraj Gupta Dilip Kumar Kala Tarun Patni Ramakant Dixit Satyadeep Verma Arjun Chandran 《The Indian journal of tuberculosis》2018,65(3):233-236
Aims and objectives
To determine the prevalence and pattern of resistance to second line drugs among multi drug resistant (MDR) tuberculosis patients being treated on category IV regimen.Methodology
This study was conducted at Department of Respiratory Medicine, J.L.N. Medical College, Ajmer in collaboration with IRL, STDC, Ajmer. Second line anti tubercular drug sensitivity for 398 multi drug resistant tuberculosis patients (between June-2015 and June-2016) was done to find out prevalence and pattern of resistance to second line drugs. Second line drug sensitivity was performed at accredited laboratory, Microbiology department, S.M.S. Medical College, Jaipur.Results
Among these 398 patients, 136 (34.17%) were resistant to fluoroquinolones (Ofloxacin) (Pre XDR); 18 (4.52%) were resistant to one of the aminoglycosides (Inj. Kanamycin, Capreomycin, Amikacin) (Pre XDR); while 22 (5.53%) patients were resistant to fluoroquinolones as well as aminoglycosides (XDR). 148 (37.18%) patients were found sensitive to both the drugs. Samples of 41 (10.3%) patients were contaminated and no growth was seen in 33 (8.29%) patients.Conclusion
Nearly half of the multi drug resistant (MDR) tuberculosis patients (44.22%) being treated on category IV regimen also have resistance to either fluoroquinolones or aminoglycosides or both i.e. Pre XDR or XDR. This may result in poor outcome of category IV regimen under RNTCP. There is a strong need for provision of culture sensitivity for all first line drugs and at least two second line drugs viz. Fluoroquinolones and aminoglycosides for all the patients registered as smear positive under RNTCP. There is also a need for development of rapid culture technique for sensitivity to second line drugs. 相似文献5.
Mi Yan Linlin Xu Yinhu Wang Jianhua Wan Ting Liu Wenjie Liu Yichao Wan Bin Zhang Rongmei Wang Qiang Li 《Drug development research》2020,81(4):402-418
Tuberculosis (TB), a chronic infectious disease, is one of the greatest risks to human beings and 10 million people were diagnosed with TB and 1.6 million died from this disease in 2017. In addition, with the emergence of multidrug-resistant tuberculosis (MDR-TB) and extensively drug-resistant tuberculosis (XDR-TB), the TB situation has become even worse, which has aggravated the mortality and spread of this disease. To overcome this problem, research into novel antituberculosis agents with enhanced activities against MDR-TB, reduced toxicity, and shortened duration of therapy is of great importance. Fortunately, many novel potential anti-TB drug candidates with five-membered rings, which are most likely to be effective against sensitive and resistant strains, have recently entered clinical trials. Different five-membered rings such as furans, pyranoses, thiazoles, pyrazolines, imidazoles, oxazolidinone, thiazolidins, isoxazoles, triazoles, oxadiazoles, thiadiazoles, and tetrazoles have been designed, prepared, and evaluated for their antimycobacterial activity against Mycobacterium tuberculosis. In this article, we highlight the recent advances made in the discovery of novel five-membered ring compounds and focus on their antitubercular activities, toxicity, structure–activity relationships, and mechanisms of action. 相似文献
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目的 分析中青年人初治耐多药肺结核患者的CT表现,探讨其影像学特点.方法 回顾性分析2013年1月至2014年12月本院经药敏试验证实的28例中青年人耐多药(观察组)及同期84例中青年人非耐药(对照组)肺结核患者的CT影像资料;运用统计学方法检验两组间影像表现差异.结果 两组间具有统计学意义的CT表现:(1)观察组少于对照组:病灶内钙化(x2 =5.60,P<0.025);(2)观察组多于对照组:肺毁损(x2=11.03,P<0.005)、胸膜钙化(x2=16.85,P<0.005)、脓气胸(x2=14.54,P<0.005)、支气管扩张(x2 =8.82,P<0.01).两组间无统计学意义的CT表现(P>0.05):斑片灶(x2=0.39)、结节灶(x2=0.9)、斑条灶(x2=2.68)、播散灶(x2=0.63)、空洞分布(x2=0.018)、多发空洞(x2=0.59)、空洞内液平(x2=0.11)、胸腔积液(x2=1.96)、纵隔肺门淋巴结肿大(x2=2.09)、纵隔肺门淋巴结钙化(x2 =0.72).结论 两组患者病灶内钙化的差异具有统计学意义(P<0.025);在肺毁损、胸膜钙化、脓气胸、支气管扩张的征象上差异具有显著统计学意义(P<0.01).在CT诊断肺结核时,除斑片、结节、斑条、播散灶及多发空洞、胸腔积液等结核征象外,如存在肺毁损、胸膜钙化、脓气胸、支气管扩张等征象,要高度怀疑为耐多药肺结核. 相似文献
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目的通过对如皋市耐多药肺结核(MDR-TB)患者的来源及转归进行分析,探索适合该地区MDR-TB的发现策略。方法 2010-2013年收集该市所有涂阳结核病患者的痰标本,开展药敏检查,分析不同来源患者中的MDR-TB发现及转归情况。结果 4年间确诊MDR-TB患者36例,结核病患者中MDR-TB检出率为9.3%,其中86.1%的MDR-TB患者来源于MDR-TB高危人群。初治凃阳者MDR-TB检出率为1.7%,MDR-TB高危人群为34.8%,差异有统计学意义(P0.001)。MDR-TB高危人群中,慢性排菌患者MDR-TB检出率为57.1%,复发患者为34.7%,其他复治患者为22.2%,2月或3月末未发现涂片仍阳性者。纳入治疗的MDR-TB患者治疗成功率为67.7%。不同来源的MDR-TB高危人群MDR-TB检出率及治疗成功率差异均无统计学意义(P0.05)。结论该市MDR-TB疫情低于全国水平,MDR-TB高危人群是该市发现耐多药肺结核最主要人群。 相似文献
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目的评价强力阿莫仙治疗耐多药肺结核的情况。方法采用中华医学会结核病分会耐多药肺结核诊断标准[1]。随机分组,69例耐多药肺结核病用强力阿莫仙治疗,为治疗组;66例耐多药肺结核采用常规抗痨药,为对照组。结果治疗2个月末痰菌阴转两组差异具有非常显著性(P〈0.01)。3个月末、6个月和12个月末痰涂阴转差异均无显著性。3个月末胸部X线检查差异有显著性(P〈0.05),6个月末和12个月末其差异分别有非常显著性(P〈0.01)。初始耐药率为52.2%,而获得性耐药率为47.8%。69例病例中,60例是暂住户口居民,9例为常住户口居民。结论强力阿莫仙对治疗肺结核治疗有效。在初结核病例中,治疗6个月末X线检查病灶吸收低于90%,或病灶边缘仍模糊,应考虑是初始耐多药病例。建议药敏试验列为肺结核综合治疗前的常规项目。 相似文献