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Dive into the research topics where Niyamat Ali Siddiqui is active.

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Featured researches published by Niyamat Ali Siddiqui.


American Journal of Tropical Medicine and Hygiene | 2010

Asymptomatic infection with visceral leishmaniasis in a disease-endemic area in bihar, India.

Roshan Kamal Topno; Vidya Nand Rabi Das; Alok Ranjan; Krishna Pandey; Dharmender Singh; Nawin Kumar; Niyamat Ali Siddiqui; Vijay P. Singh; Shreekant Kesari; Narendra Kumar; Sanjeev Bimal; Annadurai Jeya Kumar; Chetram Meena; Ranjeet Kumar; Pradeep Das

A prospective study was carried out in a cohort of 355 persons in a leishmaniasis-endemic village of the Patna District in Bihar, India, to determine the prevalence of asymptomatic persons and rate of progression to symptomatic visceral leishmaniasis (VL) cases. At baseline screening, 50 persons were positive for leishmaniasis by any of the three tests (rK39 strip test, direct agglutination test, and polymerase chain reaction) used. Point prevalence of asymptomatic VL was 110 per 1,000 persons and the rate of progression to symptomatic cases was 17.85 per 1,000 person-months. The incidence rate ratio of progression to symptomatic case was 3.36 (95% confidence interval [CI] = 0.75-15.01, P = 0.09) among case-contacts of VL compared with neighbors. High prevalence of asymptomatic persons and clinical VL cases and high density of Phlebotomus argentipes sand flies can lead to transmission of VL in VL-endemic areas.


Transactions of The Royal Society of Tropical Medicine and Hygiene | 2011

Asymptomatic infection of visceral leishmaniasis in hyperendemic areas of Vaishali district, Bihar, India: a challenge to kala-azar elimination programmes

V. N. R. Das; Niyamat Ali Siddiqui; Rakesh Bihari Verma; Roshan Kamal Topno; Dharmendra Singh; Sushmita Das; Alok Ranjan; Krishna Pandey; Nawin Kumar; Pradeep Das

A cohort of 91 asymptomatic individuals with visceral leishmaniasis (VL) were identified during base line screening using recombinant 39-aminoacid antigen (rk-39) and polymerase chain reaction (PCR) conducted from December 2005 to June 2006 involving 997 individuals of two highly endemic villages of Vaishali district, Bihar. The point prevalence of asymptomatic infection was 98 per 1000 persons at baseline. There was no statistically significant difference between rk-39 and PCR positivity rate (P>0.05), even though PCR positivity alone was found significantly higher (4.2%) than rk-39 positivity alone (2.6%). The monthly follow-up of the asymptomatic cohort revealed a disease conversion rate of 23.1 per 100 persons within a year. There was a statistically significant difference in conversion of disease when individuals were positive by both tests as compared to single tests by rk-39 and PCR (P<0.01). Disease conversion rate in the subjects residing in households with a history of VL (62%, 13/21) was higher than those residing in the households without a history of VL (38%, 8/21). Most of the identified asymptomatic individuals were from low socio-economic strata similar to that of VL cases in general. Apart from rk-39, PCR may be considered for screening of asymptomatic Leishmania donovani infection in large-scale epidemiological studies. Screening of asymptomatic cases and their close follow-up to ascertain early detection and treatment of VL may be considered in addition to the existing VL control strategies.


Tropical Medicine & International Health | 2010

The economic impact of visceral leishmaniasis on rural households in one endemic district of Bihar, India

Rhonda Sarnoff; Jaikishan Desai; Philippe Desjeux; Atul Mittal; Roshan Kamal Topno; Niyamat Ali Siddiqui; Arvind Pandey; Dipika Sur; Pradeep Das

Objective To estimate the economic burden of visceral leishmaniasis (VL) on the rural population of one VL endemic district of Bihar, the state with 85% of India’s cases.


Tropical Medicine & International Health | 2010

Annual incidence of visceral leishmaniasis in an endemic area of Bihar, India

Pradeep Das; Steven Samuels; Philippe Desjeux; Atul Mittal; Roshan Kamal Topno; Niyamat Ali Siddiqui; Dipika Sur; Arvind Pandey; Rhonda Sarnoff

The study presents the findings of a population‐based survey of the annual incidence of visceral leishmaniasis (VL) in the rural areas of one VL‐endemic district in Bihar, India. Stratified multi‐stage sampling was applied in the selection of blocks, villages, hamlets, and households. We screened 15 178 households (91 000 individuals) in 80 villages in 7 of 27 administrative blocks of the district, East Champaran. We identified 227 VL cases that occurred in the past 12 months: 149 treated individuals who survived, 14 who died from VL, and 64 active cases. The high‐incidence stratum had an estimated incidence of 35.6 cases per 10 000 persons per year (90% CI: 27.7–45.7). The annual incidence rate in the medium stratum areas was 16.8 cases per 10 000 (90% CI: 9.3–30.6). The combined annual incidence rate for the high and medium areas combined was 21.9 cases per 10 000 per year, (90% CI: 14.0–34.2). The Government of India’s VL elimination goal is to reduce the VL incidence to one case per 10 000 at the sub‐district level; thus, a 35‐fold reduction will be required in those areas with the highest VL incidence.


Therapeutics and Clinical Risk Management | 2008

A controlled, randomized nonblinded clinical trial to assess the efficacy of amphotericin B deoxycholate as compared to pentamidine for the treatment of antimony unresponsive visceral leishmaniasis cases in Bihar, India

Vidya Nand Rabi Das; Niyamat Ali Siddiqui; Krishna Pandey; Vijay P. Singh; Roshan Kamal Topno; Dharmendra Singh; Rakesh Bihari Verma; Alok Ranjan; Prabhat Kumar Sinha; Pradeep Das

Background: There is significant variation in Amphotericin B (AMB) efficacy and relapses in antimony unresponsive visceral leishmaniasis (VL) cases over a period of time (10–15 years). Keeping in mind the above mentioned view this study was undertaken with an objective to assess the magnitude of cure and relapse rates of AMB in the treatment of antimony unresponsive VL cases. Methods: In a controlled, randomized nonblinded clinical trial, we evaluated the cure and relapse rate of Amphotericin B deoxycholate as compared to pentamidine. A total of 82 sodium stibogluconate (SSG) unresponsive and parasitologically confirmed VL cases were included in this study and randomized into two groups, test (Amphotericin B) and control (Pentamidine). Both the groups were treated with recommended dosages (as per World Health Organization guidelines) of respective medicines. All the patients were followed up on 1st, 2nd, and 6th month after end of treatment. Results: Apparent cure rate in the Amphotericin B group was found to be 95% (39/41) compared with 83% (34/41) in the Pentamidine group, which shows significant statistical difference (p = 0.05). The ultimate cure rate was found 92% (38/41) in the Amphotericin B group compared to 73% (30/41) in the Pentamidine group, which shows a significant statistical difference (Yates corrected chi-square = 4.42, p = 0.04). Similarly, significant statistical difference was observed in the relapse rate of the Amphotericin group compared to the Pentamidine group (p = 0.03). Conclusions: AMB may still be the drug of choice in the management of resistant VL cases in Bihar, India. This is due to its consistent apparent cure rate (95%), low relapse rate (2.5%), and cost effectiveness compared with other available antileishmanial drugs. It is a safe drug even in case of pregnancy. Efforts should be taken to form a future strategy so that this drug and coming newer drugs do not meet a similar fate as has happened to SSG and pentamidine over a span of 10–15 years.


American Journal of Tropical Medicine and Hygiene | 2012

Clinical epidemiologic profile of a cohort of post-kala-azar dermal leishmaniasis patients in Bihar, India.

Vidya Nand Rabi Das; Alok Ranjan; Krishna Pandey; Dharmendra Singh; Neena Verma; Sushmita Das; Chandra Shekhar Lal; Naresh K. Sinha; Rakesh Bihari Verma; Niyamat Ali Siddiqui; Pradeep Das

Post-kala-azar dermal leishmaniasis (PKDL) has important public health implications for transmission of visceral leishmaniasis (VL). Clinical and epidemiologic profiles of 102 PKDL patients showed that median age of males and females at the time of diagnosis was significantly different (P = 0.013). A significant association was observed between family history of VL and sex of PKDL patients (χ(2) = 5.72, P < 0.01). Nearly 33% of the patients showed development of PKDL within one year of VL treatment. The observed time (median = 12 months) between appearance of lesions and diagnosis is an important factor in VL transmission. A significant association was observed between type of lesions and duration of appearance after VL treatment (χ(2) = 6.59, P = 0.001). Because PKDL was observed during treatment with all currently used anti-leishmanial drugs, new drug regimens having high cure rates and potential to lower the PKDL incidence need to be investigated.


BMC Public Health | 2012

Active case detection in national visceral leishmaniasis elimination programs in Bangladesh, India, and Nepal: feasibility, performance and costs

M. Mamun Huda; Siddhivinayak Hirve; Niyamat Ali Siddiqui; Paritosh Malaviya; Megha Raj Banjara; Pradeep Das; Sangeeta Kansal; Chitra Kumar Gurung; Eva Naznin; Suman Rijal; Byron Arana; Axel Kroeger; Dinesh Mondal

BackgroundActive case detection (ACD) significantly contributes to early detection and treatment of visceral leishmaniasis (VL) and post kala-azar dermal leishmaniasis (PKDL) cases and is cost effective. This paper evaluates the performance and feasibility of adapting ACD strategies into national programs for VL elimination in Bangladesh, India and Nepal.MethodsThe camp search and index case search strategies were piloted in 2010-11 by national programs in high and moderate endemic districts / sub-districts respectively. Researchers independently assessed the performance and feasibility of these strategies through direct observation of activities and review of records. Program costs were estimated using an ingredients costing method.ResultsAltogether 48 camps (Bangladesh-27, India-19, Nepal-2) and 81 index case searches (India-36, Nepal-45) were conducted by the health services across 50 health center areas (Bangladesh-4 Upazillas, India-9 PHCs, Nepal-37 VDCs). The mean number of new case detected per camp was 1.3 and it varied from 0.32 in India to 2.0 in Bangladesh. The cost (excluding training costs) of detecting one new VL case per camp varied from USD 22 in Bangladesh, USD 199 in Nepal to USD 320 in India. The camp search strategy detected a substantive number of new PKDL cases. The major challenges faced by the programs were inadequate preparation, time and resources spent on promoting camp awareness through IEC activities in the community. Incorrectly diagnosed splenic enlargement at camps probably due to poor clinical examination skills resulted in a high proportion of patients being subjected to rK39 testing.ConclusionNational programs can adapt ACD strategies for detection of new VL/PKDL cases. However adequate time and resources are required for training, planning and strengthening referral services to overcome challenges faced by the programs in conducting ACD.


Journal of Clinical Microbiology | 2012

Post-Kala-Azar Dermal Leishmaniasis in a Patient Treated with Injectable Paromomycin for Visceral Leishmaniasis in India

Krishna Pandey; V. N. R. Das; Dharmendra Singh; Sushmita Das; C. S. Lal; Neena Verma; Sanjiva Bimal; Roshan Kamal Topno; Niyamat Ali Siddiqui; Rakesh Bihari Verma; P. K. Sinha; Pradeep Das

ABSTRACT Post kala-azar dermal leishmaniasis (PKDL) is a skin manifestation that usually develops after treatment of visceral leishmaniasis (VL), a major public health problem in India. The diagnosis and management of PKDL is complex. This is the first case report from India in which PKDL occurred after paromomycin treatment for VL in an Indian patient.


BMC Infectious Diseases | 2015

Visceral leishmaniasis diagnosis and reporting delays as an obstacle to timely response actions in Nepal and India

Jan Peter Boettcher; Yubaraj Siwakoti; Ana Milojkovic; Niyamat Ali Siddiqui; Chitra Kumar Gurung; Suman Rijal; Pradeep Das; Axel Kroeger; Megha Raj Banjara

BackgroundTo eliminate visceral leishmaniasis (VL) in India and Nepal, challenges of VL diagnosis, treatment and reporting need to be identified. Recent data indicate that VL is underreported and patients face delays when seeking treatment. Moreover, VL surveillance data might not reach health authorities on time. This study quantifies delays for VL diagnosis and treatment, and analyses the duration of VL reporting from district to central health authorities in India and Nepal.MethodsA cross-sectional study conducted in 12 districts of Terai region, Nepal, and 9 districts of Bihar State, India, in 2012. Patients were interviewed in hospitals or at home using a structured questionnaire, health managers were interviewed at their work place using a semi-structured questionnaire and in-depth interviews were conducted with central level health managers. Reporting formats were evaluated. Data was analyzed using two-tailed Mann-Whitney U or Fisher’s exact test.Results92 VL patients having experienced 103 VL episodes and 49 district health managers were interviewed. Patients waited in Nepal 30 days (CI 18-42) before seeking health care, 3.75 times longer than in Bihar (8d; CI 4-12). Conversely, the lag time from seeking health care to receiving a VL diagnosis was 3.6x longer in Bihar (90d; CI 68-113) compared to Nepal (25d; CI 13-38). The time span between diagnosis and treatment was short in both countries. VL reporting time was in Nepal 19 days for sentinel sites and 76 days for “District Public Health Offices (DPHOs)”. In Bihar it was 28 days for “District Malaria Offices”. In Nepal, 73% of health managers entered data into computers compared to 16% in Bihar. In both countries reporting was mainly paper based and standardized formats were rarely used.ConclusionsTo decrease the delay between onset of symptoms and getting a proper diagnosis and treatment the approaches in the two countries vary: In Nepal health education for seeking early treatment are needed while in Bihar the use of private and non-formal practitioners has to be discouraged. Reinforcement of VL sentinel reporting in Bihar, reorganization of DPHOs in Nepal, introduction of standardized reporting formats and electronic reporting should be conducted in both countries.


Journal of Tropical Medicine | 2012

Visceral Leishmaniasis Clinical Management in Endemic Districts of India, Nepal, and Bangladesh

Megha Raj Banjara; Siddhivinayak Hirve; Niyamat Ali Siddiqui; Narendra Kumar; Sangeeta Kansal; M. Mamun Huda; Pradeep Das; Suman Rijal; Chitra Kumar Gurung; Paritosh Malaviya; Byron Arana; Axel Kroeger; Dinesh Mondal

Background. National VL Elimination Programs in India, Nepal and Bangladesh face challenges as home-based Miltefosine treatment is introduced. Objectives. To study constraints of VL management in endemic districts within context of national elimination programs before and after intervention. Methods. Ninety-two and 41 newly diagnosed VL patients were interviewed for clinical and provider experience in 2009 before and in 2010 after intervention (district training and improved supply of diagnostics and drugs). Providers were assessed for adherence to treatment guidelines. Facilities and doctor-patient consultations were observed to assess quality of care. Results. Miltefosine use increased from 33% to 59% except in Nepal where amphotericin was better available. Incorrect dosage and treatment interruptions were rare. Advice on potential side effects was uncommon but improved significantly in 2010. Physicians did not rule out pregnancy prior to starting Miltefosine. Fever measurement or spleen palpation was infrequently done in Bangladesh but improved after intervention (from 23% to 47%). Physician awareness of renal or liver toxicity as Miltefosine side effects was lower in Bangladesh. Bio-chemical monitoring was uncommon. Patient satisfaction with services remained low for ease of access or time provider spent with patient. Health facilities were better stocked with rK39 kits and Miltefosine in 2010.

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Pradeep Das

Rajendra Memorial Research Institute of Medical Sciences

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Krishna Pandey

Rajendra Memorial Research Institute of Medical Sciences

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Rakesh Bihari Verma

Rajendra Memorial Research Institute of Medical Sciences

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Roshan Kamal Topno

Rajendra Memorial Research Institute of Medical Sciences

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Chandra Shekhar Lal

Rajendra Memorial Research Institute of Medical Sciences

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Dharmendra Singh

Rajendra Memorial Research Institute of Medical Sciences

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Vidya Nand Rabi Das

Rajendra Memorial Research Institute of Medical Sciences

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Alok Ranjan

Rajendra Memorial Research Institute of Medical Sciences

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Neena Verma

Rajendra Memorial Research Institute of Medical Sciences

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Arvind Pandey

Indian Council of Medical Research

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