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Randomized controlled trial of standard versus double dose cotrimoxazole for childhood pneumonia in Pakistan.

机译:标准和双重剂量曲美唑对巴基斯坦儿童肺炎的随机对照试验。

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摘要

OBJECTIVE: Increasing concern over bacterial resistance to cotrimoxazole, which is recommended by WHO as a first-line drug for treating non-severe pneumonia, led to the suggestion that this might not be optimal therapy. However, changing to alternative antimicrobial agents, such as amoxicillin, is costly. We compared the clinical efficacy of twice-daily cotrimoxazole in standard versus double dosage for treating non-severe pneumonia in children. METHODS: A randomized controlled multicentre trial was implemented in seven hospital outpatient departments and two community health programmes. A total of 1143 children aged 2-59 months with non-severe pneumonia were randomly allocated to receive 4 mg trimethoprim plus 20 mg sulfamethoxazole/kg of body weight or 8 mg trimethoprim plus 40 mg sulfamethoxazole/kg of body weight orally twice-daily for 5 days Treatment failure occurred when a child required a change of therapy, died or was lost to follow-up. Children required a change of therapy if their condition worsened (they developed chest indrawing or danger signs) or if at 48 hours after enrollment, their clinical condition was the same (defined as having a respiratory rate that was 5 breaths/minute higher or lower than at the time of enrollment). FINDINGS: The results of 1134 children were analysed: 578 were assigned to the standard dose of cotrimoxazole and 556 to the double dose. Treatment failed in 112 children (19.4%) in the standard group and 118 (21.2%) in the double-dose group (relative risk 1.10; 95% confidence interval = 0.87-1.37). Using multivariate analysis we found that treatment was more likely to fail in children who were not given the medicine correctly (P = 0.001), in those younger than 12 months (P = 0.004), those who had used antibiotics previously (P = 0.002), those whose respiratory rate was > or =20 breaths/minute above the age-specific cut-off point (P = 0.006), and those from urban areas (P = 0.042). CONCLUSION: Both standard and double strength cotrimoxazole were equally effective in treating non-severe pneumonia. Close follow-up of patients is essential to prevent worsening of disease. Definitions of clinical failure need to be more specific. Surveillance in both rural and urban areas is essential in the development of treatment policies that are based on clinical outcomes.
机译:目的:世卫组织推荐将它作为治疗非重症肺炎的一线药物,越来越关注细菌对甲氧咪唑的耐药性,这提示这可能不是最佳疗法。然而,更换为替代的抗微生物剂,例如阿莫西林是昂贵的。我们比较了标准剂量和双剂量每日两次cotrimoxazole治疗儿童非严重肺炎的临床疗效。方法:在七个医院门诊部和两个社区卫生计划中实施了一项随机对照的多中心试验。总共随机分配1143名2至59个月大的非严重肺炎患儿,每天口服两次,分别口服4 mg甲氧苄啶+ 20 mg磺胺甲恶唑/ kg体重或8 mg甲氧苄啶+ 40 mg磺胺甲恶唑/ kg体重。 5天,当一个孩子需要改变治疗方法,死亡或失去后续治疗时,发生治疗失败。如果儿童的病情恶化(他们出现胸部抽搐或危险迹象),或者入院后48小时,他们的临床病情相同(定义为呼吸频率高于或低于5次呼吸/分钟),则需要更改治疗方案。在注册时)。结果:对1134名儿童的结果进行了分析:578例为卡曲美唑标准剂量,556例为双倍剂量。标准组112例儿童(19.4%)和双剂量组118例儿童(21.2%)治疗失败(相对危险度1.10; 95%置信区间= 0.87-1.37)。通过多变量分析,我们发现,未正确使用药物的儿童(P = 0.001),未满12个月的儿童(P = 0.004),以前使用过抗生素的儿童(P = 0.002)更有可能导致治疗失败,呼吸速率高于或高于特定年龄的临界点的呼吸频率大于或等于20呼吸/分钟的患者(P = 0.006),以及城市地区的患者(P = 0.042)。结论:标准和双重强度cotrimoxazole治疗非严重肺炎均有效。密切随访患者对于预防疾病恶化至关重要。临床失败的定义需要更具体。在制定基于临床结果的治疗政策时,农村和城市地区的监视都是必不可少的。

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