Study objectives: The aim of this study was to evaluate the psychological a
nd psychosocial impact of tracheostomy on the caregivers of patients who ha
ve undergone tracheostomies.
Setting: Rehabilitation facility.
Participants: Sixty-three lay caregivers of inpatients and outpatients with
various underlying diseases who have undergone tracheostomies.
Methods: At the beginning of the study, the 63 caregivers completed a previ
ously validated questionnaire designed to assess the problems related to ca
ring for patients with chronic diseases. Approximately 1 year later, 40 of
the 63 caregivers completed the same questionnaire a second time, The resul
ts were analyzed statistically in order to investigate the caregivers' perc
eptions of the factors associated with their Own particular situation.
Results: The answers of the 40 subjects who completed the questionnaire twi
ce revealed the existence of perceived strain persisting over time, which w
as greater in female caregivers and in those caring for patients who had ha
d a tracheostomy for < 14 months. The younger caregivers (age < 59 years) a
nd those caring for patients receiving nocturnal ventilation expressed a co
ntinuing need for information about the disease. Finally, the caregivers sa
id that they, as well as their patients led very restricted personal lives.
Conclusions: Tracheostomy causes a substantial amount of caregiver strain,
which should be taken into account when deciding on any treatment plan.