Gupte M D, Murthy B N, Mahmood K, Meeralakshmi S, Nagaraju B, Prabhakaran R
National Institute of Epidemiology, Mayor VR Ramanathan Road, Chetpet, Chennai-600 031,Tamil Nadu, India.
Int J Epidemiol. 2004 Apr;33(2):344-8. doi: 10.1093/ije/dyh024.
The concept of elimination of an infectious disease is different from eradication and in a way from control as well. In disease elimination programmes the desired reduced level of prevalence is set up as the target to be achieved in a practical time frame. Elimination can be considered in the context of national or regional levels. Prevalence levels depend on occurrence of new cases and thus could remain fluctuating. There are no ready pragmatic methods to monitor the progress of leprosy elimination programmes. We therefore tried to explore newer methods to answer these demands. With the lowering of prevalence of leprosy to the desired level of 1 case per 10000 population at the global level, the programme administrators' concern will be shifted to smaller areas e.g. national and sub-national levels. For monitoring this situation, we earlier observed that lot quality assurance sampling (LQAS), a quality control tool in industry was useful in the initially high endemic areas. However, critical factors such as geographical distribution of cases and adoption of cluster sampling design instead of simple random sampling design deserve attention before LQAS could generally be recommended. The present exercise was aimed at validating applicability of LQAS, and adopting these modifications for monitoring leprosy elimination in Tamil Nadu state, which was highly endemic for leprosy.
A representative sample of 64000 people drawn from eight districts of Tamil Nadu state, India, with maximum allowable number of 25 cases was considered, using LQAS methodology to test whether leprosy prevalence was at or below 7 per 10000 population. Expected number of cases for each district was obtained assuming Poisson distribution. Goodness of fit for the observed and expected cases (closeness of the expected number of cases to those observed) was tested through chi(2). Enhancing factor (design effect) for sample size was obtained by computing the intraclass correlation.
The survey actually covered a population of 62157 individuals, of whom 56469 (90.8%) were examined. Ninety-six cases were detected and this number far exceeded the critical value of 25. The number of cases for each district and the number of cases in the entire surveyed area both followed Poisson distribution. The intraclass correlation coefficients were close to zero and the design effect was observed to be close to one.
Based on the LQAS exercises leprosy prevalence in the state of Tamil Nadu in India was above 7 per 10000. LQAS method using clusters was validated for monitoring leprosy elimination in high endemic areas. Use of cluster sampling makes this method further useful as a rapid assessment procedure. This method needs to be tested for its applicability in moderate and low endemic areas, where the sample size may need increasing. It is further possible to consider LQAS as a monitoring tool for elimination programmes with respect to other disease conditions.
消除传染病的概念不同于根除,在某种程度上也不同于控制。在疾病消除计划中,设定了在实际时间框架内要实现的期望患病率降低水平作为目标。可以在国家或地区层面考虑消除。患病率水平取决于新病例的发生情况,因此可能会波动。目前尚无实用的方法来监测麻风病消除计划的进展。因此,我们试图探索新的方法来满足这些需求。随着全球麻风病患病率降至每10000人口1例的期望水平,计划管理者的关注点将转移到更小的区域,如国家和次国家层面。为了监测这种情况,我们早些时候观察到,工业中的质量控制工具——批量质量保证抽样(LQAS)在最初的高流行地区是有用的。然而,在普遍推荐LQAS之前,病例的地理分布以及采用整群抽样设计而非简单随机抽样设计等关键因素值得关注。本次研究旨在验证LQAS的适用性,并采用这些改进措施来监测印度泰米尔纳德邦的麻风病消除情况,该邦曾是麻风病的高流行地区。
采用LQAS方法,从印度泰米尔纳德邦的8个区抽取了64000人的代表性样本,以检验麻风病患病率是否达到或低于每10000人口7例,最大允许病例数为25例。假设服从泊松分布,计算每个区的预期病例数。通过卡方检验观察病例的拟合优度(预期病例数与观察病例数的接近程度)。通过计算组内相关系数获得样本量的增强因子(设计效应)。
该调查实际覆盖了62157人,其中56469人(90.8%)接受了检查。共检测到96例病例,这一数字远远超过了临界值25。每个区的病例数以及整个调查区域的病例数均服从泊松分布。组内相关系数接近零,观察到设计效应接近1。
基于LQAS研究,印度泰米尔纳德邦的麻风病患病率高于每10000人口7例。使用整群抽样的LQAS方法在高流行地区监测麻风病消除情况得到了验证。整群抽样的使用使该方法作为一种快速评估程序更有用。该方法在中度和低度流行地区的适用性需要进行测试,在这些地区可能需要增加样本量。进一步可以考虑将LQAS作为其他疾病状况消除计划的监测工具。