Associate Professor of Pediatrics, Ohio State University
Pediatric Pulmonology
Dr. Karen S. McCoy, MD
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Dr. Karen S. McCoy is an expert in the field of Pediatric Pulmonology. He went to University of North Carolina at Chapel Hill School of Medicine. University of North Carolina at Chapel Hill School of Medicine is a top medical university. University of North Carolina at Chapel Hill School of Medicine is ranked 22/2 in Research/PrimaryCare. He over the years received 2 awards: "America's Top Doctors" and "Fellow (FAAP)". Karen McCoy is a published doctor. He published 59 publications, including: 'Recurrent deep venous thrombosis complicating PICC line placement in two patients with cystic fibrosis and activated protein C-resistance.'
Publications
- Pulmonary Artery Pressure and Benefit of Lung Transplantation in Adult Cystic Fibrosis Patients.
- High-risk age window for mortality in children with Cystic fibrosis after lung transplantation.
- Changes in Pulmonary Function and Controlled Ventilation-High Resolution CT of Chest After Antibiotic Therapy in Infants and Young Children with Cystic Fibrosis.
- Ivacaftor improves appearance of sinus Disease on computerised tomography in cystic fibrosis patients with G551D mutation.
- Improvement of Hepatic Steatosis in Cystic Fibrosis with Ivacaftor Therapy.
- Computed tomography correlates with improvement with ivacaftor in Cystic fibrosis patients with G551D mutation.
- CT Imaging of Pediatric Patients with Cystic Fibrosis on Ivacaftor Therapy.
- Resolution of Cystic Fibrosis-related Diabetes with Ivacaftor Therapy.
- Pulmonary Hypertension in Cystic Fibrosis with Advanced Lung Disease.
- Improvement in Bronchiectasis on CT Imaging in a Pediatric Patient with Cystic Fibrosis on Ivacaftor Therapy.
- Osteopathic manipulative treatment for inpatients with Pulmonary exacerbations of cystic fibrosis: effects on spirometry findings and patient assessments of breathing,...
- Stigma and optimism in adolescents and young adults with Cystic fibrosis.
- Impact of Pulmonary hypertension on survival in patients with cystic fibrosis undergoing lung transplantation: An analysis of the UNOS registry.
- Children with Cystic Fibrosis Have Prolonged Chemical Clearance of Acid Reflux Compared to Symptomatic Children Without Cystic Fibrosis.
- Right heart catheterization measuring central hemodynamics in Cystic fibrosis during exercise.
- Demographics, Clinical Course, and Outcomes of Children with Status Asthmaticus Treated in a Pediatric Intensive Care Unit: 8-Year Review.
- Targeting bacterial integration host factor to disrupt biofilms associated with Cystic fibrosis.
- Outcomes of surgical management of severe GERD in patients with Cystic fibrosis.
- Health Literacy and Willingness to Use Online Health Information by Teens with Asthma and Diabetes.
- Inpatient healthcare trends among adult Cystic fibrosis patients in the U.S.
- Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with Cystic fibrosis homozygous for the F508del-CFTR mutation.
- Pseudomonas aeruginosa antibiotic susceptibility during long-term use of aztreonam for inhalation solution (AZLI).
- An 18-month study of the safety and efficacy of repeated courses of inhaled aztreonam lysine in Cystic fibrosis.
- Efficacy and safety of inhaled aztreonam lysine for airway pseudomonas in Cystic fibrosis.
- Inhaled aztreonam lysine for Chronic airway Pseudomonas aeruginosa in cystic fibrosis.
- Compounded colistimethate as possible cause of fatal acute Respiratory distress syndrome.
- Gas trapping in normal infants and in infants with Cystic fibrosis.
- A comparison of the therapeutic effectiveness of and preference for postural drainage and percussion, intraPulmonary percussive ventilation, and high-frequency chest w...
- Developmental delays and Pulmonary disease severity in cystic fibrosis.
- Predicting episodes of poor Asthma control in treated patients with Asthma.
- Pulmonary function is compromised in children with mediastinal lymphoma.
- Gender related differences in airway tone in children.
- Spirometric and endoscopic evaluation of airway collapse in infants with bronchoPulmonary dysplasia.
- A phase I study of adenovirus-mediated transfer of the human Cystic fibrosis transmembrane conductance regulator gene to a lung segment of individuals with Cystic fibr...
- Bronchopexy for congenital bronchomalacia in the newborn.
- Lateral thoracic expansion for Jeune's asphyxiating dystrophy: a new approach.
- Prolonged parenteral nutrition for Cystic fibrosis patients.
- Effects of feeding on protein turnover in healthy children and in children with Cystic fibrosis.
- Recurrent deep venous thrombosis complicating PICC line placement in two patients with Cystic fibrosis and activated protein C-resistance.
- Managed care and the Cystic fibrosis patient.
- Feeding-induced changes in energy expenditure in children with Cystic fibrosis.
- Elevated hepatic glucose production in children with Cystic fibrosis.
- Splanchnic uptake of leucine in healthy children and in children with Cystic fibrosis.
- Effects of tolbutamide on growth and body composition of nondiabetic children with Cystic fibrosis.
- Genome mosaicism is conserved but not unique in Pseudomonas aeruginosa isolates from the airways of young children with Cystic fibrosis.
- Copper enzyme activities in Cystic fibrosis before and after copper supplementation plus or minus zinc.
- Presentation of bronchial mucoepidermoid carcinoma as unilateral hyperlucent lung.
- Aztreonam (for inhalation solution) for the treatment of Chronic lung infections in patients with cystic fibrosis: an evidence-based review.
- Update on antibiotics for infection control in Cystic fibrosis.
- Lungs in infants and young children: improved thin-section CT with a noninvasive controlled-ventilation technique--initial experience.
- Burkholderia cenocepacia O polysaccharide chain contributes to caspase-1-dependent IL-1beta production in macrophages.
- The clinical spectrum of Chronic appendiceal abscess in cystic fibrosis.
- Autophagy stimulation by rapamycin suppresses lung inflammation and infection by Burkholderia cenocepacia in a model of Cystic fibrosis.
- Assessing bronchodilator responsiveness in infants using partial expiratory flow-volume curves.
- Bronchodilator responsiveness in normal infants and young children.
- Functional residual capacity (FRC) measurements by plethysmography and helium dilution in normal infants.
- A phase 2 study of aztreonam lysine for inhalation to treat patients with Cystic fibrosis and Pseudomonas aeruginosa infection.
- The role of computerized order sets in pediatric inpatient Asthma treatment.
Schools
University Of North Carolina Chapel Hill School Of Medicine
N Carolina Meml Hospital
Ariz Health Scis Center
Procedures Preformed
- Bronchoscopy
- Ventilation Management
Conditions Treated
- Asthma
- Bronchitis
- Bronchospasm
- COPD (Chronic Obstructive Pulmonary Disease)
- View All
Doctors Specialties
- Pediatric Pulmonology
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Pathway X Tiered Hosp/Ind Direct Access OH
- Anthem Blue Cross Blue Shield HMO
- Anthem Blue Cross Blue Shield PPO
- Assurant Health
- Blue Card PPO
- Blue Cross Blue Shield of Illinois PPO
- Group Employees PPO
- CareSource
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- Coventry Health America PPO
- Gateway Health Plan
- Humana
- Medicaid
- Medical Mutual of Ohio POS
- Medicare MCR
- Molina
- Mutual of Omaha
- NGS CoreSource
- PHP-Physicians Health Plan
- Tricare
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
- Wells Fargo Insurance
Awards
- America's Top Doctors
- Fellow (FAAP)
Education
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University of Arizona -
University of North Carolina Hospitals -
University of North Carolina at Chapel Hill School of Medicine
Hospital
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Nationwide Children's Hospital -
Ohio State University Wexner Medical Center
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