Author/Authors :
Fredrik Hja¨rthag، نويسنده , , Lars Helldin، نويسنده , , Ulla Karilampi ?
Torsten Norlander، نويسنده ,
Abstract :
Background Previous research has shown that symptom
severity often implies an increased family burden. Few
other illness-related variables have, however, been investigated
in this context. This study investigates how family
burden is affected by symptom, function, and cognition, as
well as how the patient perceives his/her illness and quality
of life.
Method A total of 99 relatives, to as many patients
diagnosed with psychosis and with their illness at a stable
level, participated in this study. The relatives estimated
their perceived burden, the patients rated the distress
caused by their illness as well as the quality of their lives,
and the care staff rated the patients’ symptom and function
as well as tested their cognitive abilities.
Results Increased family burden can be tied to the
patients’ increased symptom severity, to their impaired
functioning as well as to the patients’ higher self ratings
regarding distress. The family burden is also connected to
the patient’s reduced working memory and reduced executive
functioning, but this connection is not totally clear
and should be further investigated. Of the variables that the
patients were rated on, it was the overall functional ability
measured with GAF that had the single most impact on
perceived family burden.
Conclusions Controlling of illness-related variables, such
as symptoms, impaired functioning, impaired working
memory and executive functioning, as well as the patients’
own experiences of distress, is important in order to lessen
the burden for the relatives. All aspects of family burden
are, however, not explained by these factors, which is why
further research within this realm is required.