Leah Mollie Savitsky

Dr. Leah Mollie Savitsky

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2019 in American Journal of Obstetrics and Gynecology
Verified
Journal Article
Closed access
EFEmily E. Fay
Emily E. Fay
JHJane E. Hitti
Jane E. Hitti
CDCarlos M. Delgado
Carlos M. Delgado
LSLeah Mollie Savitsky
Leah Mollie Savitsky
EMElizabeth B. Mills
Elizabeth B. Mills
LBLaurent A. Bollag
Laurent A. Bollag

Verified
Journal Article
Open access
PDF file
BCBrahm Seymour Coler
Brahm Seymour Coler
OSOksana Shynlova
Oksana Shynlova
ABAdam Boros-Rausch
Adam Boros-Rausch
SLStephen Lye
Stephen Lye
SMStephen McCartney
Stephen McCartney
KWKristina Adams Waldorf
Kristina Adams Waldorf
Preterm birth (PTB) remains the leading cause of infant morbidity and mortality. Despite 50 years of research, therapeutic options are limited and many lack clear efficacy. Tocolytic agents are drugs that briefly delay PTB, typically to allow antenatal corticosteroid administration for accelerating fetal lung maturity or to transfer patients to high-level care facilities. Globally, there is an unmet need for better tocolytic agents, particularly in low- and middle-income countries. Although most tocolytics, such as betamimetics and indomethacin, suppress downstream mediators of the parturition pathway, newer therapeutics are being designed to selectively target inflammatory checkpoints with the goal of providing broader and more effective tocolysis. However, the relatively small market for new PTB therapeutics and formidable regulatory hurdles have led to minimal pharmaceutical interest and a stagnant drug pipeline. In this review, we present the current landscape of PTB therapeutics, assessing the history of drug development, mechanisms of action, adverse effects, and the updated literature on drug efficacy. We also review the regulatory hurdles and other obstacles impairing novel tocolytic development. Ultimately, we present possible steps to expedite drug development and meet the growing need for effective preterm birth therapeutics.

30 May 2020 in Clinical Infectious Diseases
Verified
Journal Article
Open access
PDF file
SLSylvia M. LaCourse
Sylvia M. LaCourse
AKAlisa Kachikis
Alisa Kachikis
MBMichela Blain
Michela Blain
LSLaVone E Simmons
LaVone E Simmons
JMJames A Mays
James A Mays
JHJane Hitti
Jane Hitti
We found low prevalence of SARS-CoV-2 (2.7% [5/188]) among pregnant and postpartum patients with universal testing. Prevalence among symptomatic patients was similar under initial targeted screening (22.2% [4/18]) and universal approaches (19.1% [8/42]). Among 170 asymptomatic patients, 2 were positive or inconclusive, respectively; repeat testing at 24 hours was negative.

16 June 2020 in American Journal of Perinatology
Verified
Journal Article
Closed access
PDF file
LSLeah Mollie Savitsky
Leah Mollie Savitsky
CACatherine M. Albright
Catherine M. Albright
Objective The health care system has been struggling to find the optimal way to protect patients and staff from coronavirus disease 2019 (COVID-19). Our objective was to evaluate the impact of two strategies on transmission of COVID-19 to health care workers (HCW) on labor and delivery (L&D). Study Design We developed a decision analytic model comparing universal COVID-19 screening and universal PPE on L&D. Probabilities and costs were derived from the literature. We used individual models to evaluate different scenarios including spontaneous labor, induced labor, and planned cesarean delivery (CD). The primary outcome was the cost to prevent COVID-19 infection in one HCW. A cost-effectiveness threshold was set at $25,000 to prevent a single infection in an HCW. Results In the base case using a COVID-19 prevalence of 0.36% (the rate in the United States at the time), universal screening is the preferred strategy because while universal PPE is more effective at preventing COVID-19 transmission, it is also more costly, costing $4,175,229 and $3,413,251 to prevent one infection in the setting of spontaneous and induced labor, respectively. For planned CD, universal PPE is cost saving. The model is sensitive to variations in the prevalence of COVID-19 and the cost of PPE. Universal PPE becomes cost-effective at a COVID-19 prevalence of 34.3 and 29.5% and at a PPE cost of $512.62 and $463.20 for spontaneous and induced labor, respectively. At a higher cost-effectiveness threshold, the prevalence of COVID-19 can be lower for universal PPE to become cost-effective. Conclusion Universal COVID-19 screening is generally the preferred option. However, in locations with high COVID-19 prevalence or where the local societal cost of one HCW being unavailable is the highest such as in rural areas, universal PPE may be cost-effective and preferred. This model may help to provide guidance regarding allocation of resources on L&D during these current and future pandemics. Key Points

7 October 2014 in Journal of the International Association of Providers of AIDS Care (JIAPAC)
Verified
Journal Article
Open access
LFLaura J. Fitzpatrick
Laura J. Fitzpatrick
DEDaniel J. Egan
Daniel J. Egan
ECEthan Cowan
Ethan Cowan
LSLeah Mollie Savitsky
Leah Mollie Savitsky
JKJohn D. Kushner
John D. Kushner
BABruce D. Agins
Bruce D. Agins
New York State (NYS) established guidelines for nonoccupational post-exposure prophylaxis (nPEP) to HIV in 1997. To assess current nPEP practices in NYS Emergency Departments (EDs), we electronically surveyed all ED directors in NYS, excluding Veterans’ Affairs hospitals, about nPEP and linkage-to-care protocols in the EDs. Basic descriptive statistics were used for analysis. The response rate was 96% (184/191). Of respondents, 88% reported evaluating any patient with a possible nonoccupational exposure to HIV, in accordance with NYS guidelines. Of these, 83% provided the patient with a starter pack of medications, while 4% neither supplied nor prescribed antiretroviral drugs in the ED. Sexually transmitted infection screening, risk reduction counseling, and education about symptoms of acute HIV seroconversion were performed inconsistently, despite NYS guidelines recommendations. Only 22% of EDs confirmed whether linkage to follow-up care was successful. Most NYS EDs prescribe nPEP to appropriate patients but full implementation of guidelines remains incomplete.

1 February 2014 in AIDS Patient Care and STDs
Verified
Journal Article
Closed access
DEDaniel J. Egan
Daniel J. Egan
ECEthan Cowan
Ethan Cowan
LFLaura Fitzpatrick
Laura Fitzpatrick
LSLeah Mollie Savitsky
Leah Mollie Savitsky
JKJohn Kushner
John Kushner
BABruce D. Agins
Bruce D. Agins
In 2010, New York (NY) passed new legislation mandating Emergency Departments (EDs) to offer HIV tests to patients 13-64 presenting for care. We evaluated the requirement's implementation and determined differences based on HIV prevalence or site-specific designated AIDS centers (DACs). We also evaluated policies for linkage to care of new HIV positive patients. An electronic survey on testing practices and linkage to care was administered to all NY EDs, excluding VA hospitals. Basic descriptive statistics were used for analysis. The response rate was 96% (184/191). All respondents knew of the legislation and 86% offered testing, but only 65% (159/184) to all patients required by the law. EDs in NYC, high prevalence areas, and DACs were more likely to offer HIV testing. Most facilities (104/159, 65%) used separate written consent despite elimination of this requirement. Most EDs (67%) used rapid testing: oral point-of-care ED testing and rapid laboratory testing. Only 61% of EDs provided results to patients while in the ED. Most (94%) had a linkage-to-care protocol. However, only 29% confirm linkage. We provide the first report of NY ED HIV testing practices since the mandatory testing law. Most EDs offer HIV testing but challenges still exist. Linkage-to-care plans are in place, but few EDs confirm it occurs.