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Aerodigestive / ENT

Also covered as: esophageal atresia · tracheoesophageal fistula · aspiration · tracheomalacia · laryngeal cleft · eosinophilic esophagitis · dysphagia · CHARGE syndrome
episodes total cited expert statements Updated Sep 9, 2026
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Content of this collection episodes
QUAD #22: What is CHARGE syndrome? with Dr. Catherine Hart
In this educational video, Dr. Catherine Hart, ENT surgeon at Cincinnati Children’s, provides an overview of CHARGE syndrome, a rare genetic disorder that affects multiple organ systems. Learn about its diagnosis, clinical features, and the
video0:59 · Nov 2024
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Aerodigestive & Esophageal Surgery: Dual Endoscopy Discussion
Dr. Todd Ponsky moderates a discussion on the role that dual endoscopy plays in visualization of tracheoesophageal fistulae.
video2:22 · Jan 2019
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Aerodigestive & Esophageal Surgery: Aspiration in TEFs
Dr. Michael Rutter moderates a discussion of tracheal esophageal fistula, aspiration, aspiration testing, and esophageal reflux.
video5:28 · Jan 2019
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QUAD #7 Anesthesia for Thoracoscopic Techniques with Dr. Nathaniel Tighe
Cincinnati Children's hosted the QUAD conference in October 2022 which was a combination of four conferences: The international organization for is Esophageal atresia, the Aerodigestive Society Conference, the Cincinnati Children's Airway c
video7:35 · Mar 2024
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Pediatric Gastroesophageal Reflux Disease
This podcast is a multidisciplinary discussion on a controversial topic, management of pediatric Gastroesophageal Reflux Disease, amongst Dr. Todd Ponsky, Dr. Rachel Rosen, and Dr. George "Whit" Holcomb.Dr. Rachel Rosen is Director of the A
podcast81:04 · Sep 2018
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Gastroesophageal Reflux Disease
This podcast is a multidisciplinary discussion on a controversial topic, management of pediatric Gastroesophageal Reflux Disease, amongst Dr. Todd Ponsky, Dr. Rachel Rosen, and Dr. George "Whit" Holcomb.Dr. Rachel Rosen is Director of the A
podcast81:04 · Dec 2020
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QUAD #25: Medical Management of Minor Laryngeal Clefts with Dr. Greg Burg
In this episode, Dr. Greg Burg, a pulmonologist at Cincinnati Children’s, discusses the medical management of minor laryngeal clefts, highlighting a comprehensive approach that includes swallow assessments, pulmonary therapies, and long-ter
video7:11 · Feb 2025
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Pediatric Tracheostomy in a 7 year old child Dr. Tamer Ashraf Wafa
In this video, Tracheostomy is demonstrated in for a seven year.The indication for the procedure was prolonged intubation. The video shows the surgeon's point of view (POV). This video is intended as an education material ans should not rep
video2:53 · Jun 2021
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Laryngeal Clefts
Dr. Michael Rutter is and ENT surgeon and the director of the Aerodigestive Center at Cincinnati Children's Hospital Medical Center. In this podcast, he discusses some surgical approaches to laryngeal clefts. This episode is available as an
video14:20 · Jun 2021
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Laryngotracheal Stenosis
The surgical management for laryngotracheal stenosis has changed a lot over recent years. Here, Dr. Michael Rutter, MD – the director of the Aerodigestive Center at Cincinnati Children’s Hospital will discuss the principles of both endoscop
video16:20 · May 2022
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QUAD #1: Cervical Tracheopexy with Dr. Alessandro de Alarcon
Cincinnati Children's hosted the QUAD conference in October 2022 which was a combination of four conferences: The international organization for is Esophageal atresia, the Aerodigestive Society Conference, the Cincinnati Children's Airway c
video5:26 · Dec 2023
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QUAD #2 Thoracoscopic Tracheopexy with Dr. Aaron Garrison
Cincinnati Children's hosted the QUAD conference in October 2022 which was a combination of four conferences: The international organization for is Esophageal atresia, the Aerodigestive Society Conference, the Cincinnati Children's Airway c
video7:36 · Jan 2024
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QUAD #4: Surgical Management of Button Battery & Caustic Ingestion with Dr. Aaron Garrison
Cincinnati Children's hosted the QUAD conference in October 2022 which was a combination of four conferences: The international organization for is Esophageal atresia, the Aerodigestive Society Conference, the Cincinnati Children's Airway c
video8:10 · Mar 2024
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QUAD #6 Slide Tracheoplasty for TEF, Otolaryngology Approach with Dr. Mike Rutter
Cincinnati Children's hosted the QUAD conference in October 2022 which was a combination of four conferences: The international organization for is Esophageal atresia, the Aerodigestive Society Conference, the Cincinnati Children's Airway c
video7:37 · Mar 2024
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QUAD #20: Endoscopic Repair of Minor Laryngeal Clefts with Dr. Catherine Hart
In this video, Dr. Catherine Hart, ENT surgeon at Cincinnati Children’s, discusses the endoscopic repair of minor laryngeal clefts, highlighting key surgical techniques and considerations. She explains the importance of accurately diagnosin
video6:01 · Nov 2024
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QUAD #5 Pharyngeal Scar Management with Dr. Doug von Allmen
Cincinnati Children's hosted the QUAD conference in October 2022 which was a combination of four conferences: The international organization for is Esophageal atresia, the Aerodigestive Society Conference, the Cincinnati Children's Airway c
video7:12 · Mar 2024
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Article of Interest: Optimal Timing of Tracheostomy in Injured Adolescents
Check out this weeks APSA article of interest, that YOU should know! Butler EK, Killien EY, Groner JI, Arbabi S, Vavilala MS, Rivara FP. Optimal Timing of Tracheostomy in Injured Adolescents. Pediatr Crit Care Med. 2021 Jul 1;22(7):629-6
video1:34 · Aug 2022
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Quick Literature Updates Episode 8
We’re back with eighth episode of "Quick Literature Updates" the podcast series that delivers the latest updates in pediatric surgery literature in a quick and digestible format. In each episode, we review four articles covering the most in
video · Jun 2023
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Esophageal Surveillance Practices in Esophageal Atresia Patients
Another article you should know by Cecilia Gigena "Esophageal Surveillance Practices in Esophageal Atresia Patients: A Survey by the Eastern Pediatric Surgery Network"  Authors: Malcolm N. Hamilton-Hall III, Dana Jungbauer, Christine
video · Jul 2023
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Tracheobronchopexy to Avoid Tracheostomy in Esophageal Atresia Patients With Severe Life-Threatening Tracheobronchomalacia
Hester F Shieh, Russell W Jennings, Thomas E Hamilton , Shawn Izadi , Benjamin Zendejas , C Jason Smithers  Background: Esophageal atresia (EA) is associated with tracheobronchomalacia (TBM), which in its most severe form, causes blue sp
video0:50 · Apr 2025
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Journal of Pediatric Surgery Article Review: 2nd Quarter (Apr-Jun) 2025
We are back with another episode of our Journal of Pediatric Surgery article review podcast. This time we have three publications from the second quarter of 2025, April, May and June issues. This time we're talking to editors Drs. George Ho
podcast16:35 · Aug 2025
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Aerodigestive & Esophageal Surgery - The Unsalvageable Esophagus & Cases
Join the multidisciplinary team from Cincinnati Children's Hospital as they review the complexities in the management of Tracheal Esophageal Fistula (TEF). This fast paced live event will feature case presentations, video, and panel discuss
video101:09 · Nov 2018
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Aerodigestive & Esophageal Surgery - Difficult Tracheal Esophageal Fistula
Dr. Todd Ponsky introduces the seminar covering complexities in the management of Tracheal Esophageal Fistula (TEF). Points of interest will include discussion around the "unsalvageable esophagus" and diagnosis of TEF. Dr. Michael Rutter, P
video120:59 · Nov 2018
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TEF Presentations (Extended): Aerodigestive & Esophageal Surgery
Dr. Michael Rutter presents multiple case studies of patients with esophageal fistulas and repair approaches to each.
video108:11 · Jan 2019
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Aerodigestive Management of Pediatric Aspiration - FULL SHOW
The Aerodigestive and Esophageal Center at Cincinnati Children’s is internationally known for our team approach to caring for children with airway and esophageal disorders. We have the multidisciplinary expertise to treat even the most comp
video157:09 · Jul 2020
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QUAD #27 - Multidisciplinary - How Do Teams Enhance Outcomes by the CCHMC ADEC Team
In this special episode from the QUAD Conference hosted by Cincinnati Children’s, Lizzy Lee takes us inside one of the world’s largest and most advanced multidisciplinary programs for children with complex airway and digestive conditions: t
video10:19 · Apr 2025
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Common questions2 answered from the recorded discussions
Tell me more about charge syndrome?

CHARGE syndrome is a rare genetic disorder caused by a CHD7 mutation on chromosome 8. The acronym represents coloboma, heart defects, atresia of the choana, retardation of growth and development, genital and/or urinary anomalies, and ear malformations. Diagnosis can be established based on clinical criteria even without confirmed CHD7 mutation testing. Notably, 80–90% of children with CHARGE syndrome will experience aspiration at some point in their lifetime, making it a significant functional/neurological cause of aspiration risk in the pediatric population.

When is tracheopexy indicated?

Tracheopexy is indicated for patients with tracheomalacia who require surgical intervention. Clinical decision-making has evolved to determine which patients will respond best to tracheopexy versus aortopexy using preoperative dynamic studies. The procedure is primarily used in non-esophageal atresia patients. Both aortopexy and tracheopexy are beneficial for tracheomalacia; preoperative dynamic imaging guides selection of the most appropriate procedure for each patient.

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Pediatric aerodigestive disease demands multidisciplinary evaluation because single-organ thinking misses the diagnosis. Infants presenting with vomiting and respiratory symptoms more often have oropharyngeal dysphagia than reflux [e289-c1, e359-c1], yet PPIs remain overused despite lack of efficacy under age 1 (infants reflux non-acidic milk) [e289-c3, e359-c3] and known harms including sepsis, NEC, and C. diff [e289-c5, e359-c5]. Eosinophilic esophagitis appears in 10% of children under 5 with respiratory symptoms [e289-c6, e359-c6], presenting as chronic cough rather than dysphagia [e289-c7, e359-c7]; dairy drives 60–70% of cases [e289-c9, e359-c9], and wrapping a child with undiagnosed EoE is catastrophic [e289-c8, e359-c11]. Laryngeal clefts are underdiagnosed—flexible bronchoscopy misses them 95% of the time; rigid bronchoscopy with probing is required . TEF patients warrant lifelong surveillance: presumed tracheomalacia until proven otherwise , at least three endoscopies (post-PPI, pre-age-10, transition to adulthood) , and awareness that two-thirds show histopathologic airway changes even without visible inflammation . Fundoplication in the aspirating child worsens outcomes—saliva pools above the wrap, triggering gagging and cough [e289-c27, e359-c36]. Blenderized feeds migrate to the antrum, reducing reflux [e289-c28, e359-c25], and minimal-mobilization Nissen technique has driven transmigration to zero in recent series [e289-c26, e359-c21]. Button batteries lodged at the aortic arch kill via coagulative necrosis and delayed aortoesophageal fistula; sentinel bleeds appear >2 weeks post-removal . For recurrent croup, the differential is asthma (39%), bacterial bronchitis (17%), or both (42%)—not isolated airway pathology .
  1. Infants with vomiting/wheezing more often have oropharyngeal dysphagia than GERD; PPIs are ineffective and harmful under age 1. [e289-c1, e289-c3, e289-c5, e359-c1, e359-c3, e359-c5]
  2. 10% of children <5 with respiratory symptoms have EoE (chronic cough, not dysphagia); never wrap without scoping. Dairy is the allergen in 60–70%. [e289-c6, e289-c7, e289-c8, e289-c9, e359-c6, e359-c7, e359-c9, e359-c11]
  3. Flexible bronchoscopy misses laryngeal clefts 95% of the time; rigid bronchoscopy with probing of the posterior commissure is required. [e739-c26]
  4. TEF patients need lifelong surveillance: presumed tracheomalacia, ≥3 endoscopies (post-PPI, pre-10, transition), and awareness that 67% have histopathologic airway changes. [e5969-c13, e5969-c14, e5969-c20]
  5. Button batteries at the aortic arch cause delayed aortoesophageal fistula (sentinel bleed >2 weeks post-removal); high-risk: age <5, diameter ≥20mm. [e7997-c21, e7997-c22, e7997-c23, e8088-c17]
For patients & families
When children have trouble breathing, swallowing, or feeding, doctors from different specialties work together to figure out what's wrong and how to help. This area of medicine is called aerodigestive care, and it focuses on the connected systems that let us breathe and eat [e5976-c16, e5388-c2]. Many children are born with conditions affecting these systems. Some babies are born with their food pipe (esophagus) not properly connected, a condition called esophageal atresia [e5976-c1, e5976-c2]. Others may have an opening between the breathing tube and food pipe, called a fistula, which can let food or liquid go into the lungs . The windpipe itself can be soft or floppy (tracheomalacia), making breathing difficult [e10201-c9, e10435-c1]. Doctors have found that many of these problems occur together, so a child with one issue often has others [e10201-c9, e5976-c6]. Physicians now understand that families benefit most when all the specialists—ear-nose-throat doctors, lung doctors, stomach doctors, feeding therapists, and surgeons—see the child together in one visit rather than separately [e6062-c19, e5976-c20]. This coordinated approach means fewer appointments, less time under anesthesia for tests, and faster answers [e5976-c21, e5976-c22]. Treatment might include surgery to repair structural problems, therapy to help with swallowing, medications to reduce inflammation, or breathing support [e10201-c25, e10201-c26]. The goal is always to help children breathe safely, eat comfortably, and grow well .
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Aerodigestive & Esophageal Surgery - The Unsalvageable Esophagus & Cases
For long-gap esophageal atresia, a gap of 2 vertebral bodies or approximately 2 centimeters is considered close enough to attempt primary anastomosis.
guidelineDan5:44 ↗
If primary anastomosis cannot be achieved at initial operation, placing the ends on tension for one week and then re-operating often allows successful closure due to stretch.
clinicalDan5:51 ↗
In experimental porcine models of endoscopic Foker (using olive beads and wire traction), pressure necrosis at the anastomotic site is the suspected cause of death.
clinicalTodd Ponsky6:32 ↗
Intraluminal magnetic anastomosis is being developed as a minimally invasive approach to long-gap atresia, with the goal of reducing pressure necrosis compared to bead-based traction.
clinicalTodd Ponsky7:00 ↗
Segmental colonic interposition (preserving distal native esophagus) reduces the risk of long-term redundancy and tortuosity compared to full-length colon interposition from cervical esophagus to stomach.
clinicalDan9:00 ↗
Segmental interposition preserves the native gastroesophageal junction, allowing potential future anti-reflux surgery at the normal GE junction rather than at a colonic-gastric anastomosis.
clinicalDan9:22 ↗
Segmental colonic interposition requires two anastomoses (one in chest, one in neck) and a thoracotomy, making it a morbid operation, but it is theoretically 'one and done.'
clinicalDan9:44 ↗
Sometimes surgeons try too hard to salvage the native esophagus, and children may do better with esophageal replacement, especially when chronic aspiration from recurrent TEFs or strictures causes severe pulmonary disease.
opinionDan11:24 ↗
When mobilizing a distal esophageal pouch off tension (e.g., from prevertebral fascia), the pouch retracts and becomes much shorter than it appeared pre-operatively.
clinicalDan12:53 ↗
Esophageal stents can compress the adjacent trachea, especially in children with tracheomalacia or when the esophagus lies directly posterior to the trachea. Always perform bronchoscopy after stent placement.
clinicalEm Gootee48:18 ↗
On CT scan, if the dilated esophagus lies immediately posterior to the malacic trachea, any esophageal distention (food bolus, stent) will compress the trachea. If the esophagus deviates to the left, tracheal compression is less likely.
clinicalBob48:58 ↗
Chronic esophageal foreign bodies (e.g., coins lodged for weeks) can cause posterior tracheal bulge and present as refractory asthma or bronchiolitis, often diagnosed late because chest X-rays are not routinely obtained in asthma protocols.
clinicalEm Gootee50:20 ↗
For recalcitrant esophageal strictures, weekly dilations (3–4 cycles) prevent fibroblasts from bridging and allow the stricture to scar open rather than closed.
clinicalEm Gootee36:29 ↗
Needle knife incision of esophageal strictures is effective for short, well-defined, non-circumferential scar bands. It should be avoided on the anterior wall in patients with prior TEF due to proximity to the trachea.
clinicalPhil35:13 ↗
Kenalog (steroid) injection after stricture dilation is preferred over mitomycin. Mitomycin at high concentrations (up to 5 mg/mL) causes tissue necrosis and has not shown superior outcomes compared to steroids.
clinicalEm Gootee33:28 ↗
Patients born with tracheoesophageal fistula, especially those with esophageal atresia, are at significantly higher risk for eosinophilic esophagitis, a non-acid inflammatory condition that causes strictures if untreated.
epidemiologicalPhil46:14 ↗
Eosinophilic esophagitis in infants is effectively managed with elemental formula, which works in approximately 95% of cases.
clinicalPhil47:14 ↗
Routine esophageal biopsies should be performed during endoscopy in TEF patients to screen for eosinophilic esophagitis, even in the absence of overt symptoms.
guidelinePhil46:53 ↗
In patients with recalcitrant anastomotic strictures and documented reflux, treating reflux with fundoplication may allow the stricture to heal. However, this approach risks making subsequent esophageal mobilization more difficult if replacement is ultimately needed.
clinicalDan43:07 ↗
Medical acid suppression (PPI) reduces gastric acid but does not stop reflux itself. A mechanical barrier (fundoplication) is required to prevent reflux of bile and other irritants.
clinicalPhil44:13 ↗
Feeding via gastrojejunal tube with gastric drainage (GJ/G) is a temporizing measure to reduce reflux into the esophagus while managing a refractory stricture.
clinicalEm Gootee45:47 ↗
Substernal colonic interposition avoids thoracotomy and is useful when the chest is heavily scarred from prior operations. However, it requires sacrificing the entire native esophagus.
clinicalDan10:27 ↗
When performing segmental colonic interposition, the choice of right vs. left colon is based on intraoperative assessment of the marginal artery; the side with better vascularity is selected.
clinicalDan66:15 ↗
Redundant colonic interposition can be revised by shortening the conduit at the distal anastomosis, dividing small branches along the colonic wall while preserving the vascular arcade.
clinicalDan72:54 ↗
Covered esophageal stents (8 mm diameter) are now available for pediatric use and may be effective for temporizing strictures or leaks. They are partially covered to reduce migration and perforation risk.
clinicalPhil38:45 ↗
In complex esophageal cases, a combined operating room evaluation with rigid bronchoscopy, flexible bronchoscopy, and EGD (often with two scopes simultaneously) provides comprehensive anatomic assessment and is safer than sequential procedures.
clinicalDan78:10 ↗
Contrast studies through the endoscope under fluoroscopy are routinely performed before attempting wire passage or dilation to confirm anatomy and avoid perforation.
clinicalPhil78:53 ↗
Esophageal bypass (leaving native esophagus in situ) is a viable option when resection would create an unreconstructible tracheal defect. A fundoplication is performed to prevent reflux into the residual esophageal pouch.
clinicalDan86:54 ↗
When performing esophageal bypass, leaving a tracheoesophageal fistula open allows native esophageal secretions to drain into the airway, preventing mucocele formation in the residual pouch.
clinicalBob87:49 ↗
Children who have been unable to swallow for years may continue to spit reflexively even after successful esophageal reconstruction. It can take weeks to months for them to relearn swallowing.
clinicalDan88:42 ↗
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