Dyspnea is a common and distressing symptom at the end-of-life in patients
with cancer and non-cancer diagnoses and is associated with decreased functionality
and poor quality of life.
Definition
The word dyspnea comes the Greek "dys-", difficulty
+ "pnoia", breathing = difficulty breathing.
The American Thoracic Society (ATS) defines dyspnea as "a
term used to characterize a subjective experience of breathing discomfort
that consists of qualitatively distinct sensations that vary in intensity."
Breathing is a special vital function in that it is involuntary but
can be partially controlled voluntarily for a short duration. You can
control your breath rate for a short spell, but you cannot make your heart
beat faster at will.
Prevalence
Dyspnea prevalence of 49.1% in a general cancer population (Dudgeon
2001)
Breathlessness was a complaint at presentation in 60%, and nearly 90%
just prior to death, in a cohort of patients with lung cancer (Muers 1993)
Of the patient population with non-cancer terminal illness, dyspnea is
a very problematic symptom in patients with end-stage lung disease (both
in obstructive and restrictive lung diseases) and in patients with advanced
congestive heart failure.
Dyspnea is associated with decreased quality of life and increased bio-psycho-socio-spiritual
distress in patients with advanced illness.
Causes
Dyspnea is often caused by complex interactions between physiological,
psychological, social, and environmental factors, and may result in secondary
physiological and behavioral responses (American
Thoracic Society 1999).
Assessment
Assessing the triggers, intensity, and quality of breathlessness determine
treatment options (Portenoy 1994).
Treatment
Treatment goal for dyspnea in palliative care setting is to improve
the patient’s quality of life as much as possible until a comfortable
death occurs. Treatment options are: