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在修订后的国家结核病控制规划中接受治疗的免疫功能正常的结核性淋巴结病患者中III类和I类的治疗结果

Outcomes of category III and I in immunocompetent patients of tuberculous lymphadenopathy treated in revised national tuberculosis control programme.

作者信息

Jain Nageen Kumar, Bajpai Ashok, Jain Shikha

机构信息

Department of Medicine, M.G.M. Medical College, Indore, India.

出版信息

Lung India. 2010 Jul;27(3):115-7. doi: 10.4103/0970-2113.68305.

Abstract

BACKGROUND

Retrospective observation analysis to evaluate the outcome of six month treatment regimen, CAT-III and CAT-I, for all patients diagnosed with tubercular lymphadenopathy at M.G.M. Medical College and M.Y. Hospital, Indore, India from January 2006 to December 2008.

MATERIALS AND METHODS

Out of 3158 cases of tuberculosis, there were 337 (10.67%) lymphnode cases; 31 (9.19%) HIV positive and 11(3.26 %) defaulters were excluded from the study. Of the remaining 295 cases of lymphadenopathy enrolled, 240 were on CAT-III and 55 cases of complicated lymphadenopathy were on CAT-I. All patients were followed for six months, to monitor response and complications. Patients with abscess formation or sinus formation underwent aspiration, AFB smear and culture sensitivity. In patients with persistent lymphadenopathy, repeat FNAC of the gland and in cases of hard lymphnode excision biopsy was done before receiving re-treatment regimen category -II or reserved drugs.

RESULT

Out of 295 patients, 212 (71.86%) responded to treatment, however, 83 (28.14%) did not show response at the end of treatment. Of the 83 patients, 54 (65.06%) responded to re-treatment regimen CAT-II, while 29 (34.93%) were found to be drug resistant and were given second line anti tubercular drugs. In the follow-up at six months and later after the end of treatment, 11 (5.18%) relapse was seen.

CONCLUSION

In our study, success rate of currently recommended regimens, category III and I under the revised national tuberculosis control programme in tubercular lymphadenopathy was 71.86%; with 28.34% of patients requiring re-treatment regimen. This requires a lager study involving more number of patients to prove adequacy of regimen.

摘要

背景

对2006年1月至2008年12月期间在印度印多尔市M.G.M.医学院和M.Y.医院被诊断为结核性淋巴结病的所有患者,采用CAT - III和CAT - I六个月治疗方案进行回顾性观察分析,以评估治疗结果。

材料与方法

在3158例结核病病例中,有337例(10.67%)为淋巴结病例;31例(9.19%)HIV阳性和11例(3.26%)未坚持治疗者被排除在研究之外。在纳入的其余295例淋巴结病病例中,240例采用CAT - III治疗,55例复杂淋巴结病病例采用CAT - I治疗。所有患者均随访六个月,以监测反应和并发症。有脓肿形成或窦道形成的患者接受抽吸、抗酸杆菌涂片和培养药敏试验。对于持续性淋巴结病患者,在接受重新治疗方案II类或储备药物治疗前,对腺体进行重复细针穿刺抽吸活检,对于坚硬淋巴结则进行切除活检。

结果

295例患者中,212例(71.86%)对治疗有反应,然而,83例(28.14%)在治疗结束时未显示反应。在这83例患者中,54例(65.06%)对重新治疗方案CAT - II有反应,而29例(34.93%)被发现耐药,并给予二线抗结核药物治疗。在治疗结束后六个月及以后的随访中,出现了11例(5.18%)复发。

结论

在我们的研究中,目前修订的国家结核病控制规划中推荐的III类和I类方案在结核性淋巴结病中的成功率为71.86%;28.34%的患者需要重新治疗方案。这需要一项涉及更多患者的更大规模研究来证明方案的充分性。

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