Norman Fenn III

Dr. Norman Fenn III

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Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

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

Representative Publications

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30 October 2017 in Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy
Verified
Journal Article
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NINorman Fenn III
Norman Fenn III
KPKimberly S Plake
Kimberly S Plake

1 September 2020 in Currents in Pharmacy Teaching and Learning
Verified
Journal Article
Closed access
AGAlessa D. Gonzales
Alessa D. Gonzales
KHKiersi S. Harmon
Kiersi S. Harmon
NINorman Fenn III
Norman Fenn III

1 June 2016 in Hospital Pediatrics
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Journal Article
Closed access
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JMJennifer Leontine Murphy
Jennifer Leontine Murphy
NINorman Fenn III
Norman Fenn III
LPLaura Pyle
Laura Pyle
HHHeather Heizer
Heather Heizer
SHShannon Hughes
Shannon Hughes
SPSarah K. Parker
Sarah K. Parker
BACKGROUND AND OBJECTIVE: Children receiving long-term antibiotic therapy (LTAT) at Children’s Hospital Colorado (CHCO) are treated with both oral and intravenous (IV) agents and often experience complications not comprehensively described by the literature. We sought to describe adverse drug events (ADEs) and venous access complications (VACs) in pediatric patients managed with oral and IV antibiotics so as to inform clinical decision-making, drug monitoring, and patient counseling at CHCO.METHODS: We conducted a retrospective review of children receiving LTAT through the CHCO infectious disease service from 2006 to 2012. Demographic, microbiologic, diagnostic data, ADEs, and VACs were recorded for each patient.RESULTS: From 2006 to 2012, 521 patients received 1876 courses, accounting for 71 306 days of antimicrobial therapy. A total of 219 patients (42 %) developed an ADE with discontinuation of the offending agent in 65% of courses associated with an ADE. The most common ADEs were neutropenia, rash, and diarrhea. Central lines were placed in 376 patients with 106 (28%) experiencing ≥1 VACs. IV agents were associated with a fourfold increase in the rate of ADEs compared with oral agents, and a fivefold increase when VACs were included.CONCLUSIONS: Practitioners may make more informed decisions and risk assessments by using descriptive ADE information for specific agents and mode of drug delivery to mitigate risk, thereby improving the quality of care. Patients should be counseled regarding risks of LTAT, including increased risk with IV therapy, and actively monitored for side effects.

28 November 2018 in Pediatric Drugs
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Journal Article
Closed access
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KOKazeem A. Oshikoya
Kazeem A. Oshikoya
GWGerold T. Wharton
Gerold T. Wharton
DADebbie Avant
Debbie Avant
SDSara L. Van Driest
Sara L. Van Driest
NINorman Fenn III
Norman Fenn III
AMAnn W. McMahon
Ann W. McMahon

1 January 2021 in Currents in Pharmacy Teaching and Learning
Verified
Journal Article
Closed access
KHKiersi S. Harmon
Kiersi S. Harmon
AGAlessa D. Gonzales
Alessa D. Gonzales
NINorman Fenn III
Norman Fenn III

1 May 2021 in Currents in Pharmacy Teaching and Learning
Verified
Journal Article
Closed access
COChimnonso P. Onuoha
Chimnonso P. Onuoha
MGMichael P. Garner
Michael P. Garner
NINorman Fenn III
Norman Fenn III