[Drug-resistant pulmonary tuberculosis at Maradi Regional Hospital Center, Niger (2014-2018)].

Medecine tropicale et sante internationale Pub Date : 2023-11-06 eCollection Date: 2023-12-31 DOI:10.48327/mtsi.v3i4.2023.438
Mahaman Laouali Harouna Amadou, Ibrahim Maman Lawan, Ousmane Abdoulaye, Abdoul Kadir Ibrahim Mamadou, Oumarou Amadou, Hassane Boureima, Biraima Ahamadou, Nouhou Hama Aghali, Nana Hadiza Abdourahamane Maifada, Abdoulaziz Kabirou Amoussa, Chaibou Maidakouale
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Abstract

Aim of study: To describe the clinical, therapeutic and evolutionary profile of patients followed for rifampicin-resistant pulmonary tuberculosis (RR-TB) at the Regional Hospital Centre (RHC) of Maradi (Niger) from 2014 to 2018.

Methods: We conducted a retrospective and descriptive study based on the records of patients followed for Multidrug-resistant tuberculosis (MDR-TB) between January 1, 2014 and June 30, 2018 at the resistant tuberculosis management unit in Maradi (Niger). This unit is located within the RHC of Maradi and has a capacity of 20 beds in 4 wards. It receives patients with tuberculosis resistant to first-line anti-tuberculosis drugs. In this study, patients diagnosed with RR-TB by genotypic (GeneXpert MTB/RIF) or phenotypic (culture) testing were included. We excluded from this study: patients previously treated for more than 1 month with second-line anti-TB drugs; patients with resistance to second-line injectables (SLI) and/or fluoroquinolones (FQ); patients with an electrocardiogram QTc greater than 500 ms (the corrected QT (QTc) estimates the QT interval at a rate of 60 beats per second); cases of atypical mycobacteriosis detected by phenotypic testing.Patients were previously on 2RHZE/4RH prior to the discovery of resistance. The treatment protocol for resistant TB was as follows: 4KmMfxPtoCfzHZE/5MfxCfzZE (The second-line injectable was replaced by Lzd in case of initial or treatment-emergent deafness). HIV co-infected patients received, in addition to anti-tuberculosis drugs, antiretrovirals and cotrimoxazole in preventive doses.

Results: A total of 80 patients were included in the present study (70 males and 10 females, mean age 34.4 years with extremes ranging from 18 to 71 years). Patients aged 18-35 years accounted for more than half. Patients with primary treatment failure were the most frequent type (36%) followed by patients with retreatment failure (24%) and patients with retreatment relapse (17%). It should be noted that 77 patients (96%) were previously treated for TB and only 3 patients (4%) were new cases. The majority of patients (70%) had a Body mass index of less than 18 kg/m2. 7.5% of patients were HIV positive, one was diabetic, 52% of the patients had grade 2 radiological lesions. Grade 1 deafness was noted at the beginning of treatment in 3%. A third of patients (36%) were primary treatment failures. The treatment protocol was as follows: 4KmMfxPtoCfzHZE/5MfxCfzZE. Only 1 patient had a positive culture at the end of the 4th month of treatment. Most of the patients had experienced adverse events, mainly digestive, with vomiting being the most common. The therapeutic success rate was 88%. We noted 10% of deaths, 1% of therapeutic failure and 1% of lost to follow-up.Six months after treatment, 48 patients (60%) were smear negative and 43 (54%) were culture negative. In 32 patients (40%), the smear was not performed and culture was not performed in 37.

Conclusion: The short treatment regime gives satisfactory results in the absence of resistance to fluoroquinolones, with rare adverse effects. In Niger, further efforts should be made to minimize the delay in diagnosis which is responsible for most deaths during treatment. A centre could usefully be designated to organize "TB consiliums" allowing any practitioner to submit difficult cases of MDR-TB.

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[尼日尔马拉迪地区医院中心耐药肺结核(2014-2018 年)]。
研究目的描述2014年至2018年期间尼日尔马拉迪地区医院中心(RHC)随访的耐利福平肺结核(RR-TB)患者的临床、治疗和演变概况:我们根据2014年1月1日至2018年6月30日期间马拉迪(尼日尔)耐多药肺结核管理单位随访的耐多药肺结核(MDR-TB)患者的记录进行了一项回顾性和描述性研究。该病房位于马拉迪地区医疗中心内,4间病房可容纳20张病床。它接收对一线抗结核药物产生耐药性的结核病患者。本研究纳入了通过基因型(GeneXpert MTB/RIF)或表型(培养)检测确诊为 RR-TB 的患者。我们将以下患者排除在本研究之外:曾接受过 1 个月以上二线抗结核药物治疗的患者;对二线注射剂(SLI)和/或氟喹诺酮类(FQ)产生耐药性的患者;心电图 QTc 超过 500 毫秒的患者(校正 QT(QTc)以每秒 60 次的速度估算 QT 间期);通过表型检测发现的非典型分枝杆菌病病例。耐药性肺结核的治疗方案如下:耐药性肺结核的治疗方案如下:4KmMfxPtoCfzHZE/5MfxCfzZE(二线注射剂由 Lzd 取代,以防初次或治疗后出现耳聋)。合并感染艾滋病毒的患者除服用抗结核药物外,还服用抗逆转录病毒药物和预防剂量的复方新诺明:本研究共纳入 80 名患者(70 名男性和 10 名女性,平均年龄为 34.4 岁,极端年龄为 18 至 71 岁)。年龄在 18-35 岁之间的患者占一半以上。初治失败的患者最多(36%),其次是再治疗失败的患者(24%)和再治疗复发的患者(17%)。值得注意的是,77 名患者(96%)曾接受过肺结核治疗,只有 3 名患者(4%)是新病例。大多数患者(70%)的体重指数低于 18 kg/m2。7.5%的患者艾滋病毒呈阳性,一人患有糖尿病,52%的患者有二级放射病变。3%的患者在治疗初期出现一级耳聋。三分之一的患者(36%)初治失败。治疗方案如下4KmMfxPtoCfzHZE/5MfxCfzZE。只有 1 名患者在治疗的第 4 个月末出现培养阳性。大多数患者出现了不良反应,主要是消化系统,其中最常见的是呕吐。治疗成功率为 88%。治疗六个月后,48 名患者(60%)涂片阴性,43 名患者(54%)培养阴性。32名患者(40%)未进行涂片检查,37名患者未进行培养:短期治疗方案在氟喹诺酮类药物无耐药性的情况下取得了令人满意的效果,不良反应极少。在尼日尔,应进一步努力减少诊断延误,因为大多数死亡病例都是由诊断延误造成的。可以指定一个中心来组织 "结核病联合会",允许任何医生提交耐多药结核病疑难病例。
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