My goal in chronic disease management is to minimize health risks, maximize health potential and interfere with life as little as possible. I always say, 'My job is to provide you with the information, then we can make the decisions together.'
Christopher Siracusa, MD



As a pediatric pulmonologist, I specialize in the care of patients with various lung conditions, specifically asthma, bronchiectasis, chronic cough, cystic fibrosis (CF) and dyspnea.

My area of expertise is cystic fibrosis. The Cystic Fibrosis Center at Cincinnati Children’s Hospital Medical Center strives to go 'above and beyond the guidelines' to set our patients up for success.

Our team uses a collaborative approach to care. We believe patients and families are the most important members of the team. Services we offer include advanced imaging, bronchoscopy, exercise testing and pulmonary function testing. We partner with researchers for atypical cystic fibrosis diagnostics — providing national and international referrals. Together with doctors at the Cincinnati Children’s Pancreas Center, we help patients with recurrent pancreatitis related to cystic fibrosis.

My goal in chronic disease management is to minimize health risks, maximize health potential and interfere with life as little as possible. I always say, "My job is to provide you with the information, then we can make the decisions together."

I was drawn to pulmonology by my interest in the physiology of the lungs. I always knew I wanted to work in pediatrics. My first interactions with cystic fibrosis patients sparked my career interest. For me, it was the right combination of interesting physiology, complicated microbiology, chronic disease management and psychosocial support. I enjoy the continuity of care I provide. It's exciting to watch a patient I have followed for many years reach life milestones like learning to walk, learning to drive or graduating from high school.

My research focuses on the psychosocial and behavioral determinants of cystic fibrosis outcomes. I am an original member of the CF Foundation’s Success with Therapies Research Consortium, formed in 2015. I serve as the principal investigator at Cincinnati Children’s for multiple, multi-center studies related to adherence patterns and barriers in cystic fibrosis. Some of my clinical research studies involve the relationship among treatment complexity, burden and clinical outcomes in cystic fibrosis.

In my free time, I enjoy traveling, cooking, hiking, watching movies, and spending time with friends and family. I have lived in downtown Cincinnati since moving here in 2012 and love to experience all the city offers.

MD: American University of the Caribbean, Netherlands, Antilles, 2009.

Residency: Akron Children’s Hospital/NEOUCOM, Akron, OH, 2012.

Services and Specialties

Pulmonary Medicine, Cystic Fibrosis

Insurance Information

Cincinnati Children's strives to accept a wide variety of health plans. Please contact your health insurance carrier to verify coverage for your specific benefit plan.

View Insurance Information


Built environment factors predictive of early rapid lung function decline in cystic fibrosis. Gecili, E; Brokamp, C; Rasnick, E; Afonso, PM; Andrinopoulou, ER; Dexheimer, JW; Clancy, JP; Keogh, RH; Ni, Y; Palipana, A; et al. Pediatric Pulmonology. 2023; 58:1501-1513.

The Cystic Fibrosis Action Plan: A low health literacy, pictographic self-management tool with clinical automation. Reeves, PT; Bennett, WC; McCown, MY; Welsh, SK; McDonald, CM; Beker, L; Robbins, S; Vitale, DS; Siracusa, C; Brownell, JN; et al. Pediatric Pulmonology. 2022; 57:2847-2850.

Genetic counseling access for parents of newborns who screen positive for cystic fibrosis: Consensus guidelines. Langfelder-Schwind, E; Raraigh, KS; Parad, RB; Balcom, JR; Birnbaum, VK; Darrah, R; Farrell, PM; Foil, K; Ghate, S; Greene, L; et al. Pediatric Pulmonology. 2022; 57:894-902.

Favorable Clinician Acceptability of Telehealth as Part of the Cystic Fibrosis Care Model during the COVID-19 Pandemic. Perkins, RC; Davis, J; NeSmith, A; Bailey, J; Powers, MR; Chaudary, N; Siracusa, C; Uluer, A; Solomon, GM; Sawicki, GS. Annals of the American Thoracic Society. 2021; 18:1588-1592.

Assessment of treatment burden and complexity in cystic fibrosis: A quality improvement project. Hente, E; Weiland, J; Mullen, L; Hawke, J; Schuler, CL; Filigno, SS; Siracusa, C. Pediatric Pulmonology. 2021; 56:1992-1999.

Patient and family perceptions of telehealth as part of the cystic fibrosis care model during COVID-19. Jaclyn, D; Andrew, NS; Ryan, P; Julianna, B; Christopher, S; Nauman, C; Powers, M; Gregory S, S; George M, S. Journal of Cystic Fibrosis. 2021; 20:e23-e28.

A Pilot Study of Mindfulness-Based Cognitive Therapy to Improve Well-Being for Health Professionals Providing Chronic Disease Care. Hente, E; Sears, R; Cotton, S; Pallerla, H; Siracusa, C; Filigno, SS; Boat, T. The Journal of Pediatrics. 2020; 224:87-93.e1.

Assessing and responding to stress related to pulmonary function testing in cystic fibrosis through quality improvement. Nusbaum, K; Filigno, SS; Feldstein, J; Hente, E; Koch, E; Mullen, L; Weiland, J; Boat, T; Siracusa, C. Pediatric Pulmonology. 2020; 55:1139-1146.

Executive functioning in pediatric cystic fibrosis: A preliminary study and conceptual model. Borschuk, AP; Molitor, S; Everhart, RS; Siracusa, C; Filigno, SS. Pediatric Pulmonology. 2020; 55:939-947.

Acute Respiratory Distress Syndrome immediately following the removal of an aspirated foreign body. Simpson, R; Myer, C; Siracusa, C. Respiratory Medicine Case Reports. 2020; 29:100978.

Patient Ratings and Comments

All patient satisfaction ratings and comments are submitted by actual patients and verified by a leading independent patient satisfaction company, NRC Health. Patient identities are withheld to ensure confidentiality and privacy. Only those providers whose satisfaction surveys are administered through Cincinnati Children’s Hospital Medical Center are displayed. Click here to learn more about our survey

Overall Patient Rating