Olesya M. Taylor
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Olesya M. Taylor has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Alyssa M. Peckham
School of Pharmacy, Center for Health Policy and Healthcare Research, Northeastern University, 360 Huntington Avenue, Boston, MA 02135, USA
1 shared publication Christine Lam
Department of Pharmacy Practice, University of the Incarnate Word Feik School of Pharmacy, San Antonio, Texas
1 shared publication- Kirk Evan Evoy
The University of Texas at Austin College of Pharmacy, Austin, USA
1 shared publication - Kunal J. Shah
Assistant Manager, Clinical Pharmacy, Morristown Medical Center, Atlantic Health System, Morristown, New Jersey
1 shared publication - Payal H. Desai
Staff Pharmacist, Department of Pharmacy, Morristown Medical Center, Atlantic Health System, Morristown, New Jersey; Medical Science Liaison, Immuno-Inflammation, GSK, Research Triangle Park, North Carolina
1 shared publication
Latest Publications
- Open Access
- 1 July 2021
- Published by American Association of Psychiatric Pharmacists (AAPP) in Mental Health Clinician
- Vol. 11 (4) , 225-230
Characterization of hospitalized patients who received naloxone while receiving opioids with or without gabapentinoids
Introduction: Gabapentin and pregabalin (gabapentinoids) can be given with opioids for opioid-sparing and adjuvant analgesic effects. In the context of certain comorbidities and high dosages, coadministration of these agents can lead to respiratory depression or oversedation, necessitating naloxone administration. Methods: A retrospective chart review from January 2015 to December 2017 was conducted to include patients who received naloxone and opioids with or without gabapentinoids. Exclusion criteria included pregnancy or having received naloxone in the emergency department, intensive care, or pediatrics units. The primary outcome was to characterize differences between groups regarding comorbidities, history of renal or hepatic dysfunction, history of SUD, opioid tolerance, initiation and dose appropriateness of gabapentinoids, and dose intensity of gabapentinoids and opioids. Secondary outcomes were concomitant CNS depressant use and naloxone episodes for documented respiratory depression. Results: Of 126 patients who met inclusion criteria, 36 received opioids and gabapentinoids (gabapentinoid group) and 90 received opioids alone (nongabapentinoid group). There were 136 naloxone episodes between the 2 groups. More than 50% of the naloxone episodes in the gabapentinoid group involved opioids of at least 90 oral morphine mg equivalents. Respiratory depression accounted for 39% and 15.8% of the naloxone episodes in the gabapentinoid and nongabapentinoid groups, respectively. Discussion: There may be increased naloxone episodes among patients receiving opioids and gabapentinoids. Future studies are needed to evaluate the incremental risk of respiratory depression and oversedation as it pertains to concomitant medication administration and patient-specific factors.
- 1 July 2021
- Published by American Association of Psychiatric Pharmacists (AAPP) in Mental Health Clinician
- Vol. 11 (4) , 225-230
Open AccessCharacterization of hospitalized patients who received naloxone while receiving opioids with or without gabapentinoids
Introduction: Gabapentin and pregabalin (gabapentinoids) can be given with opioids for opioid-sparing and adjuvant analgesic effects. In the context of certain comorbidities and high dosages, coadministration of these agents can lead to respiratory depression or oversedation, necessitating naloxone administration. Methods: A retrospective chart review from January 2015 to December 2017 was conducted to include patients who received naloxone and opioids with or without gabapentinoids. Exclusion criteria included pregnancy or having received naloxone in the emergency department, intensive care, or pediatrics units. The primary outcome was to characterize differences between groups regarding comorbidities, history of renal or hepatic dysfunction, history of SUD, opioid tolerance, initiation and dose appropriateness of gabapentinoids, and dose intensity of gabapentinoids and opioids. Secondary outcomes were concomitant CNS depressant use and naloxone episodes for documented respiratory depression. Results: Of 126 patients who met inclusion criteria, 36 received opioids and gabapentinoids (gabapentinoid group) and 90 received opioids alone (nongabapentinoid group). There were 136 naloxone episodes between the 2 groups. More than 50% of the naloxone episodes in the gabapentinoid group involved opioids of at least 90 oral morphine mg equivalents. Respiratory depression accounted for 39% and 15.8% of the naloxone episodes in the gabapentinoid and nongabapentinoid groups, respectively. Discussion: There may be increased naloxone episodes among patients receiving opioids and gabapentinoids. Future studies are needed to evaluate the incremental risk of respiratory depression and oversedation as it pertains to concomitant medication administration and patient-specific factors.
- Open Access
- 1 January 2020
- Published by Elsevier in Current Therapeutic Research
- Vol. 93, 100596
The Effect of Dipeptidyl Peptidase-4 Inhibitors on Macrovascular and Microvascular Complications of Diabetes Mellitus: A Systematic Review
- 1 January 2020
- Published by Elsevier in Current Therapeutic Research
- Vol. 93, 100596
Open AccessThe Effect of Dipeptidyl Peptidase-4 Inhibitors on Macrovascular and Microvascular Complications of Diabetes Mellitus: A Systematic Review