Nila A Sathe

ORCID: 0000-0002-8243-6988
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About
Contact & Profiles
Research Areas
  • Autism Spectrum Disorder Research
  • Family and Disability Support Research
  • Health Systems, Economic Evaluations, Quality of Life
  • Child Nutrition and Feeding Issues
  • Health Sciences Research and Education
  • Pharmaceutical studies and practices
  • Meta-analysis and systematic reviews
  • Global Health Workforce Issues
  • Uterine Myomas and Treatments
  • Food Security and Health in Diverse Populations
  • Attention Deficit Hyperactivity Disorder
  • Metabolism and Genetic Disorders
  • Dysphagia Assessment and Management
  • Maternal and fetal healthcare
  • Public Health Policies and Education
  • Child and Adolescent Psychosocial and Emotional Development
  • Obstructive Sleep Apnea Research
  • Health Policy Implementation Science
  • Geriatric Care and Nursing Homes
  • Behavioral and Psychological Studies
  • Cerebral Palsy and Movement Disorders
  • Electronic Health Records Systems
  • Tumors and Oncological Cases
  • Congenital Heart Disease Studies
  • Reliability and Agreement in Measurement

RTI International
2023-2025

University of North Carolina at Chapel Hill
2011-2025

University of Ottawa
2024

Georgia College & State University
2024

Bruyère
2024

Vivekananda Global University
2023

National University Hospital
2022

Premier Research Group
2018-2021

Vanderbilt University Medical Center
2004-2020

Vanderbilt University
2017-2018

This guide is derived from the information in chapter 6 of The Cochrane Handbook (1, 2). Carol Lefebvre, Eric Manheimer and Julie Glanville kindly gave permission to original Campbell Collaboration (Campbell) Information Retrieval Guide authors use updates as basis for this guide. In 2015 Methods Group (IRMG) revised reflect current areas practice recommendations Methodological Expectations Intervention Reviews (MEC2IR), capture evolving strategies searching, update links descriptions...

10.4073/cmg.2016.1 article EN cc-by Campbell Systematic Reviews 2017-01-01

In 2011, an Advanced Notice of Proposed Rulemaking proposed that de-identified human data and specimens be included in biobanks only if patients provide consent. The National Institutes Health Genomic Data Sharing policy went into effect 2015, requiring broad consent from almost all research participants.We conducted a systematic literature review attitudes toward biobanking, consent, sharing. Bibliographic databases MEDLINE, Web Science, EthxWeb, GenETHX. Study screening was using...

10.1038/gim.2015.138 article EN cc-by-nc-nd Genetics in Medicine 2015-11-19

Importance Child maltreatment is associated with serious negative physical, psychological, and behavioral consequences. Objective To review the evidence on primary care–feasible or referable interventions to prevent child inform US Preventive Services Task Force. Data Sources PubMed, Cochrane Library, trial registries through February 2, 2023; references, experts, surveillance December 6, 2023. Study Selection English-language, randomized clinical trials of youth age 18 years (or their...

10.1001/jama.2024.0276 article EN JAMA 2024-03-19

Social needs interventions aim to improve health outcomes and mitigate inequities by addressing health-related social needs, such as lack of transportation or food insecurity. However, it is not clear whether these studies are reducing racial ethnic inequities.

10.1001/jamanetworkopen.2022.50654 article EN cc-by-nc-nd JAMA Network Open 2023-01-19
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