Back to Authors

Caballero, Anyull D. B.

0000-0002-5294-6100

Mayo Clinic

Jacksonville College

Citations 3

Beyond the Impact of Cadaveric Donor Transplant on Chronic Rhinosinusitis and Recalcitrant Disease
Candelo, Estephanía , Bohorquez‐Caballero, Anyull D. , Avila‐Castano, Karol , Donaldson, Angela M. , Wadei, Hani, Donaldson, Angela M , Gomez, Estephania Candelo , Caballero, Anyull D. B. , Wadei, Hani M.

International Forum of Allergy & Rhinology | May 22, 2025 | Volume: 15 | Issue: 6 | Pages: 671-672

10.1002/alr.23593 Get It

Real‐World Evaluation of Asthma Severity Following Endoscopic Sinus Surgery in Chronic Rhinosinusitis Patients
Caballero, Anyull D. B. , Candelo, Estephanía , Avila‐Castano, Karol , Alhalabi, Alaa , Donaldson, Angela M. , Bohorquez‐Caballero, Anyull D. , Gomez, Estephania Candelo , Donaldson, Angela M

OTO Open | September 18, 2024 | Volume: 8 | Issue: 3 | Pages: No page available

10.1002/oto2.70013 Get It

AbstractObjectiveThis study aimed to evaluate the impact of endoscopic sinus surgery (ESS) on asthma severity up to 12 months after surgical intervention.Study DesignRetrospective cohort.SettingTertiary care center.MethodsPatients with a history of asthma and Chronic Rhinosinusitis (CRS) who underwent ESS between 2013 and 2023 were included. Asthma severity was assessed according to current Global Initiative for Asthma (GINA) guidelines, classifying patients into mild, moderate, and severe based on medication requirements. Asthma severity was evaluated up to 3 months prior to ESS and 1‐year post‐ESS. Patients with aspirin‐exacerbated respiratory disease (AERD) were excluded. Statistical analysis was performed using McNemar test and Wilcoxon signed‐rank test to assess differences in asthma severity, medication doses, and number of medications.ResultsSixty‐five patients were included, of which 44 (67.7%) had CRS with nasal polyps (CRSwNP) and 21 (32.3%) had CRS without nasal polyps (CRSsNP). No significant differences were found in asthma severity pre‐ and post‐ESS (P = .175). Similarly, no differences were found in ICS doses (P = .999), total number of prescribed medications (P = .157) or presence of exacerbations before and after ESS (P = .078). However, a significant increase in time from last rescue inhaler use was noted after ESS, increasing from a median of 6.71 to 23.1 weeks (P = .004).ConclusionThis study is the first to assess the impact of ESS on asthma severity in a real‐world setting. Our findings suggest that ESS does not impact asthma severity classification. However, it might provide relief of asthma symptoms in the early postoperative period.
The impact of cadaveric donor transplant on the development of chronic rhinosinusitis and recalcitrant disease
Candelo, Estephanía , Bohorquez‐Caballero, Anyull D. , Avila‐Castano, Karol , Wadei, Hani M. , Donaldson, Angela M. , Wadei, Hani, Gomez, Estephania Candelo , Caballero, Anyull D. B. , Wadei, Hani M

International Forum of Allergy & Rhinology | August 24, 2024 | Volume: 14 | Issue: 12 | Pages: 1953-1956

10.1002/alr.23429 Get It

Key points The study found a higher incidence of chronic rhinosinusitis (CRS) and recalcitrant CRS in cadaveric organ transplant recipients compared to those receiving living donor transplants. Recipients of cadaveric transplants were 1.32 times more likely to develop CRS and 1.68 times more likely to develop medically recalcitrant CRS. Living kidney transplants significantly reduced the risk of developing CRS (OR = 0.12) and recalcitrant CRS (OR = 0.11), highlighting a potentially protective effect against these conditions. In contrast, cadaveric liver transplants were associated with an increased risk of CRS and medically recalcitrant CRS. Kaplan–Meier survival analysis indicated a significant difference in time to CRS onset between cadaveric and living donor transplants. Median time to CRS onset was longer for living donor recipients (21.1 months) compared to cadaveric recipients (15.6 months). This study underscores the need for transplant teams and otolaryngologist to consider donor type during transplant follow‐up due to differing risks of CRS development.