International and Multicenter Prospective Controlled Study of Dysphagia After Anterior Cervical Spine Surgery

Author:

Falavigna Asdrubal12,Arruda André de Oliveira13ORCID,Righesso Neto Orlando1,Dozza Diego4,Guyot Juan Pablo5,Yurac Ratko6,Jalón Pablo Gustavo7,Avila José Maria Jiménez89,Zárate Barón10,Scheverin Nicolas11,Ghogawala Zoher12

Affiliation:

1. Postgraduation Program in Health Sciences, University of Caxias do Sul, Caxias do Sul, Brazil;

2. Department of Neurosurgery, University of Caxias do Sul, Caxias do Sul, Brazil;

3. Cajuru University Hospital, Spine Surgery Unit, Curitiba, Brazil;

4. São Vicente de Paulo Hospital, Neurosurgery Unit, Passo Fundo, Brazil;

5. Hospital Universitario Fundación Favaloro, Spine Surgery, Buenos Aires, Argentina;

6. Department of Traumatology—Spine Unit, Clínica Alemana, Santiago, Chile;

7. Department of Neurosurgery—Spine Surgery, Hospital de Clínicas José de San Martin—University of Buenos Aires, Buenos Aires, Argentina;

8. Department of Orthopedics and Traumatology, Hospital de Especialidades, Guadalajara, Mexico;

9. Instituto Tecnológico y de Estudios Superiores de Monterrey, Campus Guadalajara, Guadalajara, Jalisco, México;

10. Spine Surgery Department, Instituto Nacional de Rehabilitación, Mexico City, Mexico;

11. Department of Orthopaedics—Spine Surgery, Hospital Dr Diego Thompsonn, Bueno Aires, Argentina;

12. Department of Neurosurgery, Professor and Chairman, Lahey Hospital and Medical Center—Tufts University School of Medicine, Burlington, USA

Abstract

BACKGROUND: In the context of anterior approach to the cervical spine, dysphagia is a common complication and still without a clear distinction of risk factors. OBJECTIVE: To analyze the risk factors of dysphagia after cervical spine surgery. METHODS: Multicenter prospective study evaluated patients who underwent anterior cervical spine surgery for degenerative pathologies, studying surgical, anesthesia, base disease, and radiological variables (preoperatively, 24 hours, 1 and 3 weeks, and 6 months after surgery), with control group matched. Postoperative dysphagia was assessed by Swallowing Satisfaction Index and Swallowing Questionnaire; besides, based on multiple logistic regression model, a risk factor analysis correlation was applied. RESULTS: In total, 233 cervical patients were evaluated; most common level approached was C5-C6 (71.8%). All showed same decreasing trade for dysphagia incidence—with more cases on cervical group (P < .05); severe cases were rare. At postoperative day 1, identified risk factors were approach to C3-C4 (4.11, P < .01), loss of preoperative cervical lordosis (2.26, P < .01), intubation attempts ≥2 (3.10, P < .01), and left side approach (1.85, P = .02); at day 7, body mass index ≥30 (2.29, P = .02), C3-C4 (3.42, P < .01), and length of surgery ≥90 minutes (2.97, P = .005); and at day 21, C3-C4 were kept as a risk factor (3.62, P < .01). CONCLUSION: A high incidence level of dysphagia was identified, having a clear decreasing trending (number of cases and severity) through postoperative time points; considering possible risk factors, strongest correlation was the approach at the C3-C4 level—statistically significant at the 24 hours, 7 days, and 21 days assessment.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Surgery

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