Chronic Obstructive Pulmonary Disease and Dysphagia: What Have We Learned So Far and What Do We Still Need to Investigate?

Author(s):  
Renata Mancopes ◽  
Fernanda Borowsky da Rosa ◽  
Lidia Lis Tomasi ◽  
Adriane S. Pasqualoto ◽  
Catriona M. Steele

Purpose Dysphagia is an underrecognized concern in people with chronic obstructive pulmonary disease (COPD) and may contribute to disease exacerbations. In this review article, we share information regarding dysphagia in people with COPD, synthesizing knowledge both from the literature and from studies performed in the context of a multidisciplinary clinical pulmonary rehabilitation program at the Federal University of Santa Maria in Brazil. Results This narrative review presents evidence showing that awareness of dysphagia and patient-reported symptoms of dysphagia are rare in individuals with stable COPD. However, evidence from the routine collection of patient-reported symptom data using the Eating Assessment Tool 10 and about dysphagia-related quality of life using the Swallowing Quality of Life questionnaire do suggest that dysphagia is experienced by some individuals with COPD. Several studies suggest that patients with stable COPD present with altered swallowing physiology on videofluoroscopic exams, including silent aspiration in a small number of these individuals. However, both patient self-report and clinical screening using the Volume–Viscosity Swallowing Test have been found to be poor predictors of these videofluoroscopic findings. We discuss the possibility that altered laryngeal sensation and respiratory–swallow discoordination play a role in dysphagia in people with COPD, and highlight assessment tasks that appear to have the highest sensitivity for detecting penetration–aspiration in this population. Finally, we review preliminary evidence suggesting that physical therapy techniques targeting altered respiratory muscle biomechanics may benefit swallowing in people with COPD. Knowledge gaps requiring further research are identified, and implications for clinical practice are discussed.

2005 ◽  
Vol 21 (3) ◽  
pp. 180-187 ◽  
Author(s):  
Samantha M.C. Pang ◽  
Kin-Sang Chan ◽  
Betty P.M. Chung ◽  
Kam-Shing Lau ◽  
Edward M.F. Leung ◽  
...  

Given the limitations of existing health-related quality-of-life (QOL) measures in capturing the end-of-life experience of patients with advanced chronic diseases, an empirically grounded instrument, the quality-of-life concerns in the end of life questionnaire (QOLC-E), was developed. Though it was built on the McGill quality of life questionnaire (MQOL), its sphere is more holistic and culturally specific for the Chinese patients in Hong Kong. One hundred and forty-nine patients with advanced chronic obstructive pulmonary disease (COPD) or metastatic cancer completed the questionnaire. Seven factors (28 items) which emerged from the factor analysis were grouped into four positive (support, value of life, food-related concerns, and healthcare concerns) and four negative (physical discomfort, negative emotions, sense of alienation, and existential distress) subscales. Good internal consistency and concurrent validity were shown. The results also revealed that these two groups of patients had similar QOL concerns. The validity of applying QOLC-E as an outcome measure to evaluate the effectiveness of palliative and psychoexistential interventions has yet to be tested.


Author(s):  
PUSHPAVALLI KOTHA ◽  
Naga Vamsi Krishna Vasabhakthula ◽  
Christine Undurthi ◽  
Siva Ganga M

Aim:  The main aim of this study is to evaluate the effect of exacerbations on the quality of life of the patients with chronic obstructive pulmonary disease. Materials and Methods: Patients of both the genders and with an age of above 18 years of patients who were diagnosed with COPD were included in this prospective study. Modified British Medical Research Council (m-MRC) Dyspnoea Scale was used to establish functional impairment due to shortness of breath in the study participants. Saint George's Respiratory Questionnaire (SGRQ) was also used to assess the patient’s overall health and quality of life-based on self-report. Results: Among the 110 study participants, 87.3% were males and 12.7% were females. It was observed that majority of the patients were in the age group 51-60 years (43.6%). The most frequently observed co-morbidities were hypertension (22.7%) followed by diabetes mellitus (19.1%). Most of the patients were observed to be with m-MRC grade-3 (42.7%) followed by m-MRC garde-2 (39.1%). The SGRQ score was observed to be increased with increase in the frequency of exacerbations. Conclusion: Clinical Pharmacist should take the responsibility in providing effective evidence based therapeutic recommendations for the better management and well being of the COPD patients.


2016 ◽  
Vol 11 ◽  
Author(s):  
Fabio Arpinelli ◽  
Mauro Carone ◽  
Riccardo Gioacchino ◽  
Giorgio Bertolotti

Background: Asthma and chronic obstructive pulmonary disease (COPD) are frequent in the general population. These diseases can worsen the quality of life of people suffering from them, limiting their daily activities and disrupting their sleep at night. Some questionnaires to measure the impact of the diseases on the daily life of patients are available. The measurements of subjective outcomes have become a part of clinical practice, and are used very frequently in clinical trials. Our aim was to describe how data on HRQoL in asthma and COPD are reported in papers published in the medical literature. Methods: We identified papers on the recent respiratory drugs (chemical, not biological), that reported the HRQoL measurement and that were published from 2009 to April 2014. We planned to describe data about HRQoL, and we had no intention of comparing the degree of efficacy of drugs. Results: The most used questionnaires are the Asthma Quality of Life Questionnaire (AQLQ) and the Saint George's Respiratory Questionnaire (SGRQ). These tools, administered at the baseline and at the end of the study (and interim evaluations in the longer studies) allowed for the identification of improvements as perceived by the patient after the treatment, even if in some cases these improvements were limited and not clinically relevant. Subjective measurements have always been placed among the secondary endpoints and the number of patients (estimated for the main endpoint) has often statistically overestimated the result. In addition, it is clear that subjective data is normally reported, but rarely commented on. Conclusions: There are some methodology aspects that should be discussed in more depth, for example the necessity to express variations in the subjective perception, not as p-value but as effect-size.


2016 ◽  
Vol 18 (3) ◽  
pp. 482 ◽  
Author(s):  
Sonia Elena Pineda Higuita ◽  
Vidal De Jesús Ramos Melchor ◽  
Daniela Cadavid Carmona

Objetivo: Describir la calidad de vida de pacientes con enfermedad pulmonar obstructiva crónica año 2014. Materiales y Métodos: Se realizó un estudio observacional descriptivo de corte transversal para evaluar la calidad de vida de los pacientes mayores de 65 años con diagnóstico de Enfermedad Pulmonar Obstructiva Crónica. La muestra correspondió a 179 usuarios de la ESE Metrosalud (Medellín), que aceptaron participar voluntariamente en el estudio. Se aplicó una encuesta estructurada que incluyó variables sociodemográficas, algunos determinantes ambientales, sociales y aspectos relacionados con la enfermedad. Igualmente se incluyó la escala de calidad de vida Saint George la cual está constituida por tres dimensiones: síntomas, actividades e impacto. Resultados: Los pacientes encuestados tenían entre 65 y 99 años de edad, al evaluar la calidad de vida con el cuestionario Saint George la dimensión más impactada fue la actividad; se obtuvo asociación estadísticamente significativa entre calidad de vida total y el nivel de escolaridad (P= 0,005), etnia (P= 0,004), y algunas variables relacionadas con la enfermedad. Conclusiones: Existe una asociación entre la calidad relacionada con la salud, según la evaluación del SGRQ y el grado de la enfermedad.AbstractObjective: To describe the quality of life of patients with chronic obstructive pulmonary disease 2014. Materials and Methods: A descriptive observational cross-sectional study was performed to evaluate the quality of life of patients older than 65 and who had a diagnosis of chronic obstructive pulmonary disease. The sample corresponded to 179 users of ESE Metrosalud (Medellín), who agreed to participate voluntarily in the study. A structured survey that included socio-demographic variables, some environmental and social determinants, and aspects related to the disease was applied. Besides, the Saint George quality of life scale was also included, which is composed of three dimensions: symptoms, activities and impact. Results: The surveyed patients were between 65 and 99 years old, when they took the Saint George quality of life questionnaire, the most impacted dimension was the activity; it was obtained a statistically significant association between total quality of life and the level of schooling (P= 0.005), ethnic group (P= 0.004), and some variables related with the disease. Conclusions: There is an association between the quality related with health, according to the evaluation of the SGRQ and the extent of the disease.


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