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Dive into the research topics where Scott E. Kellerman is active.

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Featured researches published by Scott E. Kellerman.


PLOS Medicine | 2010

HIV testing for children in resource-limited settings: what are we waiting for?

Scott E. Kellerman; Shaffiq M. Essajee

Scott Kellerman and Shaffiq Essajee argue that the time has come to increase access to HIV testing for children, especially in sub-Saharan Africa.


AIDS | 2013

Beyond early infant diagnosis: case finding strategies for identification of HIV-infected infants and children.

Saeed Ahmed; Maria H. Kim; Nandita Sugandhi; Phelps Br; Sabelli R; Diallo Mo; Young P; Duncan D; Scott E. Kellerman

There are 3.4 million children infected with HIV worldwide, with up to 2.6 million eligible for treatment under current guidelines. However, roughly 70% of infected children are not receiving live-saving HIV care and treatment. Strengthening case finding through improved diagnosis strategies, and actively linking identified HIV-infected children to care and treatment is essential to ensuring that these children benefit from the care and treatment available to them. Without attention or advocacy, the majority of these children will remain undiagnosed and die from complications of HIV. In this article, we summarize the challenges of identifying HIV-infected infants and children, review currently available evidence and guidance, describe promising new strategies for case finding, and make recommendations for future research and interventions to improve identification of HIV-infected infants and children.


AIDS | 2013

Linkage, initiation and retention of children in the antiretroviral therapy cascade: an overview.

Phelps Br; Saeed Ahmed; Anouk Amzel; Diallo Mo; Jacobs T; Scott E. Kellerman; Maria H. Kim; Nandita Sugandhi; Melanie Tam; Wilson-Jones M

In 2012, there were an estimated 2 million children in need of antiretroviral therapy (ART) in the world, but ART is still reaching fewer than 3 in 10 children in need of treatment. [1, 7] As more HIV-infected children are identified early and universal treatment is initiated in children under 5 regardless of CD4, the success of pediatric HIV programs will depend on our ability to link children into care and treatment programs, and retain them in those services over time. In this review, we summarize key individual, institutional, and systems barriers to diagnosing children with HIV, linking them to care and treatment, and reducing loss to follow-up (LTFU). We also explore how linkage and retention can be optimally measured so as to maximize the impact of available pediatric HIV care and treatment services.


AIDS | 2013

Beyond prevention of mother-to-child transmission: keeping HIV-exposed and HIV-positive children healthy and alive.

Scott E. Kellerman; Saeed Ahmed; Theresa Feeley-Summerl; Jonathan Jay; Maria H. Kim; Emilia Koumans; Lydia Lu; Ryan Phelps; Nandita Sugandhi; Erik J Schouten; Mike Tolle; Fatima Tsiouris; Children

In 2011, Joint United Nations Programme on HIV/AIDS announced a plan to eliminate new HIV infections among children by 2015. This increased focus on the elimination of maternal to child transmission (MTCT) is most welcome but is insufficient, as access to prevention of MTCT (PMTCT) programming is neither uniform nor universal. A new and more expansive agenda must be articulated to ensure that those infants and children who will never feel the impact of the current elimination agenda are reached and linked to appropriate care and treatment. This agenda must addresses challenges around both reducing vertical transmission through PMTCT and ensuring access to appropriate HIV testing, care, and treatment for all affected children who were never able to access PMTCT programming. Option B+, or universal test and treat for HIV-infected pregnant women is an excellent start, but it may be time to rethink our current approaches to delivering PMTCT services. New strategies will reduce vertical transmission to less than 1% for those mother-infant pairs who can access them allowing for the contemplation of not just PMTCT, but actual elimination of MTCT. But expanded thinking is needed to ensure elimination of pediatric HIV.


AIDS | 2013

HIV Exposed Infants: Rethinking care for a lifelong condition

Nandita Sugandhi; Jessica Rodrigues; Maria H. Kim; Saeed Ahmed; Anouk Amzel; Mike Tolle; Eric J. Dziuban; Scott E. Kellerman; Emilia Rivadeneira

Each year over a million infants are born to HIV-infected mothers. With scale up of prevention of mother-to-child transmission (PMTCT) interventions, only 210 000 of the 1.3 million infants born to mothers with HIV/AIDS in 2012 became infected. Current programmatic efforts directed at infants born to HIV-infected mothers are primarily focused on decreasing their risk of infection, but an emphasis on maternal interventions has meant follow-up of exposed infants has been poor. Programs are struggling to retain this population in care until the end of exposure, typically at the cessation of breastfeeding, between 12 and 24 months of age. But HIV exposure is a life-long condition that continues to impact the health and well being of a child long after exposure has ended. A better understanding of the impact of HIV on exposed infants is needed and new programs and interventions must take into consideration the long-term health needs of this growing population. The introduction of lifelong treatment for all HIV-infected pregnant women is an opportunity to rethink how we provide services adapted for the long-term retention of mother–infant pairs.


PLOS ONE | 2014

Evaluating the Impact of Prevention of Mother-to-Child Transmission of HIV in Malawi through Immunization Clinic-Based Surveillance

Michele Sinunu; Erik J Schouten; Nellie Wadonda-Kabondo; Enock Kajawo; Michael Eliya; Kundai Moyo; Frank Chimbwandira; Lee Strunin; Scott E. Kellerman

Background Prevention of mother-to-child transmission of HIV (PMTCT) programs can greatly reduce the vertical transmission rate (VTR) of HIV, and Malawi is expanding PMTCT access by offering HIV-infected pregnant women life-long antiretroviral therapy (Option B+). There is currently no empirical data on the effectiveness of Malawian PMTCT programs. This study describes a surveillance approach to obtain population-based estimates of the VTR of infants <3 months of age in Malawi immediately after the adoption of Option B+. Methods and Findings A sample of caregivers and infants <3 months from 53 randomly chosen immunization clinics in 4 districts were enrolled. Infant dried blood spot (DBS) samples were tested for HIV exposure with an antibody test to determine maternal seropositivity. Positive samples were further tested using DNA PCR to determine infant infection status and VTR. Caregivers were surveyed about maternal receipt of PMTCT services. Of the 5,068 DBS samples, 764 were ELISA positive indicating 15.1% (14.1–16.1%) of mothers were HIV-infected and passed antibodies to their infant. Sixty-five of the ELISA-positive samples tested positive by DNA PCR, indicating a vertical transmission rate of 8.5% (6.6–10.7%). Survey data indicates 64.8% of HIV-infected mothers and 46.9% of HIV-exposed infants received some form of antiretroviral prophylaxis. Results do not include the entire breastfeeding period which extends to almost 2 years in Malawi. Conclusions The observed VTR was lower than expected given earlier modeled estimates, suggesting that Malawi’s PMTCT program has been successful at averting perinatal HIV transmission. Challenges to full implementation of PMTCT remain, particularly around low reported antiretroviral prophylaxis. This approach is a useful surveillance tool to assess changes in PMTCT effectiveness as Option B+ is scaled-up, and can be expanded to track programming effectiveness for young infants over time in Malawi and elsewhere.


AIDS | 2013

Understanding the contribution of common childhood illnesses and opportunistic infections to morbidity and mortality in children living with HIV in resource-limited settings

Surbhi Modi; Alex Chiu; Bernadette Ng’eno; Scott E. Kellerman; Nandita Sugandhi; Lulu Muhe

Objective:Although antiretroviral treatment (ART) has reduced the incidence of HIV-related opportunistic infections among children living with HIV, access to ART remains limited for children, especially in resource-limited settings. This paper reviews current knowledge on the contribution of opportunistic infections and common childhood illnesses to morbidity and mortality in children living with HIV, highlights interventions known to improve the health of children, and identifies research gaps for further exploration. Design and Methods:Literature review of peer-reviewed articles and abstracts combined with expert opinion and operational experience. Results:Morbidity and mortality due to opportunistic infections has decreased in both developed and resource-limited countries. However, the burden of HIV-related infections remains high, especially in sub-Saharan Africa, where the majority of HIV-infected children live. Limitations in diagnostic capacity in resource-limited settings have resulted in a relative paucity of data on opportunistic infections in children. Additionally, the reliance on clinical diagnosis means that opportunistic infections are often confused with common childhood illnesseswhich also contribute to excess morbidity and mortality in these children. Although several preventive interventions have been shown to decrease opportunistic infection-related mortality, implementation of many of these interventions remains inconsistent. Conclusions:In order to reduce opportunistic infection-related mortality, early ART must be expanded, training for front-line clinicians must be improved, and additional research is needed to improve screening and diagnostic algorithms.


Journal of the International AIDS Society | 2015

Integration of HIV in child survival platforms: a novel programmatic pathway towards the 90-90-90 targets

Dick Chamla; Shaffiq Essajee; Mark Young; Scott E. Kellerman; Ronnie Lovich; Nandita Sugandhi; Anouk Amzel; Chewe Luo

Integration of HIV into child survival platforms is an evolving territory with multiple connotations. Most literature on integration of HIV into other health services focuses on adults; however promising practices for children are emerging. These include the Double Dividend (DD) framework, a new programming approach with dual goal of improving paediatric HIV care and child survival. In this commentary, the authors discuss why integrating HIV testing, treatment and care into child survival platforms is important, as well as its potential to advance progress towards global targets that call for, by 2020, 90% of children living with HIV to know their status, 90% of those diagnosed to be on treatment and 90% of those on treatment to be virally suppressed (90–90–90).


PLOS Medicine | 2016

Building from the HIV Response toward Universal Health Coverage

Jonathan Jay; Kent Buse; Marielle Hart; David Wilson; Robert Marten; Scott E. Kellerman; Morolake Odetoyinbo; Jonathan D. Quick; Timothy G Evans; Peter Piot; Mark Dybul; Agnes Binagwaho

Jonathan Jay and colleagues draw lessons from the the global HIV response that could help guide the universal health coverage movement.


AIDS | 2013

Pediatric treatment 2.0: ensuring a holistic response to caring forHIV-exposed and infected children

Shaffiq Essajee; Stephen M. Arpadi; Eric J. Dziuban; Raul Gonzalez-Montero; Shirin Heidari; David Jamieson; Scott E. Kellerman; Emilia H. Koumans; Atieno Ojoo; Emilia Rivadeneira; Stephen A. Spector; Helena Walkowiak

Treatment 2.0 is an initiative launched by UNAIDS and WHO in 2011 to catalyze the next phase of treatment scale-up for HIV. The initiative defines strategic activities in 5 key areas, drugs, diagnostics, commodity costs, service delivery and community engagement in an effort to simplify treatment, expand access and maximize program efficiency. For adults, many of these activities have already been turned into treatment policies. The recent WHO recommendation to use a universal first line regimen regardless of gender, pregnancy and TB status is a treatment simplification very much in line with Treatment 2.0. But despite that fact that Treatment 2.0 encompasses all people living with HIV, we have not seen the same evolution in policy development for children. In this paper we discuss how Treatment 2.0 principles can be adapted for the pediatric population. There are several intrinsic challenges. The need for distinct treatment regimens in children of different ages makes it hard to define a one size fits all approach. In addition, the fact that many providers are reluctant to treat children without the advice of specialists can hamper decentralization of service delivery. But at the same time, there are opportunities that can be availed now and in the future to scale up pediatric treatment along the lines of Treatment 2.0. We examine each of the five pillars of Treatment 2.0 from a pediatric perspective and present eight specific action points that would result in simplification of pediatric treatment and scale up of HIV services for children.

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Maria H. Kim

Baylor College of Medicine

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Saeed Ahmed

Baylor College of Medicine

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Anouk Amzel

United States Agency for International Development

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Emilia Rivadeneira

Centers for Disease Control and Prevention

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Eric J. Dziuban

Baylor College of Medicine

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Emilia H. Koumans

Centers for Disease Control and Prevention

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