Abstract Objective The outbreak of the COVID-19 pandemic had a considerable impact on the healthcare access, treatment, and follow-up of oncologic patients. The aim of this study was to evaluate how the COVID-19 pandemic has affected consultation and follow-up demand as well as treatment volume at Brazilian Head and Neck Surgery centers. Methods An anonymous online questionnaire was used for collection of data across all Brazilian Head and Neck Surgery Centers across a 3-month period (April‒June 2021). This information included the characteristics of each center, and the perceived self-reported impact of the COVID-19 pandemic on academic activities, residency training, and the diagnosis, treatment, and follow-up of patients with Head and Neck diseases between 2019 and 2020. Results The response rate across the 40 registered Brazilian Head and Neck Surgery Centers was 47.5% (n = 19). The data showed a significant reduction in the total number of consultations (24.8%) and number of attending patients (20.2%) between 2019 and 2020. The total number of diagnostic exams (31.6%) and surgical procedures (13.0%) conducted over this period also decreased significantly. Conclusions The COVID-19 pandemic had a significant national impact on Brazilian Head and Neck Surgery Centers. Future studies should examine the long-term effects of the pandemic on cancer treatment. Level of evidence Evidence from a single descriptive study. COVID19 COVID 19 COVID-1 access followup follow up centers 3month month 3 April‒June AprilJune April June 2021. 2021 . 2021) center selfreported self reported activities training diagnosis 201 2020 4 475 47 5 47.5 n 19. 19) 24.8% 248 24 8 (24.8% 20.2% 202 20 2 (20.2% 31.6% 316 31 6 (31.6% 13.0% 130 13 0 (13.0% significantly longterm long term COVID1 1 COVID- 47. 24.8 (24.8 20.2 (20.2 31.6 (31.6 13.0 (13.0 24. (24. 20. (20. 31. (31. 13. (13. (24 (20 (31 (13 (2 (3 (1 (

Resumo Introdução: O câncer de cabeça e pescoço representa 3% de todos os tipos de neoplasias malignas e o carcinoma espinocelular corresponde a 90% dos casos. Há estudos sobre a qualidade de vida desses pacientes, mas pouco se conhece sobre os prejuízos físico e emocional dos seus cuidadores. Objetivo: Avaliar a qualidade de vida de pacientes com câncer de cabeça e pescoço e comparativamente de seus cuidadores a partir da aplicação de questionários validados. Método: A casuística foi constituída de 30 pacientes com tumores avançados (carcinomas espinocelulares de estádio III ou IV) de cabeça e pescoço e 30 cuidadores. Foram aplicados questionários específicos (Coop/Wonca, EORTC QLQ-C30, EORTC H&N35, Coop/Wonca e Caregiver Strain Index - CSI) a partir de visitas de rotina ao ambulatório. Resultados: Dos 30 pacientes, 28 eram do sexo masculino e 25 apresentavam estádio IV, com idade média de 56,6 anos. 36,7% tinham o tumor primário na orofaringe e 70% sentiam dor. As escalas funcionais cognitivas, física e emocional foram as mais afetadas. Dor, fadiga e distúrbio do sono foram os sintomas mais prevalentes. Dos 30 cuidadores, 23 eram do sexo feminino e 70% eram cuidadores primários. 36,7% dos cuidadores apresentaram alto nível de estresse, principalmente relacionado à sensação de incapacidade. A comparação entre pacientes e cuidadores demonstram que os dois grupos apresentam semelhante comprometimento da qualidade de vida: aptidão física (p = 0,487), saúde mental (p = 0,615), atividades diárias (p = 0,793), atividades sociais (p = 0,301), mudança na saúde (p = 0,649), saúde geral (p = 0,168). Conclusão: O comprometimento na qualidade de vida é semelhante entre pacientes e seus cuidadores, ou seja, não só os indivíduos de fato doentes apresentam prejuízo na sua qualidade de vida, mas os seus cuidadores também e na mesma proporção.

Abstract Introduction: Head and neck cancer represents 3% of all the types of malignant neoplasms and squamous cell carcinoma (SCC) is responsible for 90% of these cases. There have been some studies evaluating the quality of life of these patients, but little is known about the physical and emotional effects on their caregivers. Objective: To evaluate the quality of life of patients with head and neck cancer and their caregivers by applying validated questionnaires. Methods: Thirty patients with advanced tumors (SCC stage III or IV) and their 30 caregivers were included. Specific questionnaires (Coop/Wonca, EORTC QLQ-C30, EORTC H&N35, Coop/Wonca, and Caregiver Strain Index - CSI) were applied during routine medical consultations. Results: Of the 30 patients, 28 were males and 25 had stage IV tumors, with mean age of 56.6 years. 36.7% had the primary tumor in the oropharynx and 70% reported pain. The functional cognitive, physical, and emotional scales were the most affected. Pain, fatigue, and sleep disorders were the most prevalent symptoms. Of the 30 caregivers, 23 were females and 70% were the primary caregivers. 36.7% of the caregivers had high levels of stress, mainly related to the feeling of incapacity. The comparison between patients and caregivers demonstrated that the two groups had similar quality of life impairment: physical fitness (p = 0.487), mental health (p = 0.615), daily activities (p = 0.793), social activities (p = 0.301), changes in health (p = 0.649), and overall health (p = 0.168). Conclusion: Quality of life impairment is similar between patients and their caregivers. This result demonstrates that not only the patients show quality of life impairment, but their caregivers also have it and at similar proportions.