Abstract:Background
Head and neck cancer is a life threatening illness requiring aversive treatments. Despite clear potential for posttraumatic stress disorder (PTSD) symptoms in both patients and their partners, research is scant.
Methods
Newly diagnosed patients and partners (no. of dyads=42) completed questionnaires to assess symptoms of PTSD, anxiety, and depression, as well as demographic, medical, and attitudinal variables.
Results
Partners had higher average levels of PTSD symptoms than patients (p=.023). Mo… Show more
“…Our results corroborate previous findings that clinicians need to be aware of PTSD symptoms in not only HNC patients but also their caregivers [6]. This is particularly important in light of evidence that caregiver distress influences patient outcomes [41,42].…”
Section: Discussionsupporting
confidence: 93%
“…Results showed that 19 % of caregivers met criteria for estimated PTSD caseness 6 months after HNC diagnosis. This rate is slightly lower than the 29 % reported in HNC caregivers between 4 and 16 weeks after HNC diagnosis [6], which is an earlier timeframe. The presence of PTSD symptoms at 6 months is consistent with the growing literature demonstrating high rates of psychological distress in HNC caregivers across the disease trajectory [3], as well as in caregivers of patients with other cancer types [26][27][28].…”
Section: Discussionmentioning
confidence: 52%
“…Previous research found that perceptions of threat held by spouses of patients with HNC were significantly related to their PTSD symptoms, representative of a medium effect size (r = .38) [6]. G-power software [17] indicated that a sample of 39 caregivers would be needed to detect a similar effect (setting power at .80 and alpha at .05) using correlation analyses.…”
Section: Power Analysismentioning
confidence: 98%
“…HNC caregivers report higher levels of perceived burden and strain at 2-6 months post-diagnosis, compared to later in the disease trajectory [11]. Only one study has identified factors that are associated with the experience of PTSD symptoms in HNC caregivers, and this found that depression and anxiety, as well as perceptions of disease threat, were associated with a greater number of symptoms [6].…”
Section: Introductionmentioning
confidence: 97%
“…Caregivers of patients with HNC also report low mood and fear of cancer recurrence [5]. Moreover, recent research has established that spouses of patients with HNC report high levels of posttraumatic stress disorder (PTSD) symptoms at diagnosis [6]. Twenty-nine percent of spouses met criteria for estimated PTSD caseness in comparison to 11 % of patients.…”
This preliminary study suggests that caregivers who have perceptions of low benefits from treatment and many patient symptoms, and those using avoidant coping strategies, are at increased risk of experiencing symptoms of PTSD. Psychological interventions that target illness perceptions and coping may help to reduce the prevalence of PTSD in caregivers of patients with HNC.
“…Our results corroborate previous findings that clinicians need to be aware of PTSD symptoms in not only HNC patients but also their caregivers [6]. This is particularly important in light of evidence that caregiver distress influences patient outcomes [41,42].…”
Section: Discussionsupporting
confidence: 93%
“…Results showed that 19 % of caregivers met criteria for estimated PTSD caseness 6 months after HNC diagnosis. This rate is slightly lower than the 29 % reported in HNC caregivers between 4 and 16 weeks after HNC diagnosis [6], which is an earlier timeframe. The presence of PTSD symptoms at 6 months is consistent with the growing literature demonstrating high rates of psychological distress in HNC caregivers across the disease trajectory [3], as well as in caregivers of patients with other cancer types [26][27][28].…”
Section: Discussionmentioning
confidence: 52%
“…Previous research found that perceptions of threat held by spouses of patients with HNC were significantly related to their PTSD symptoms, representative of a medium effect size (r = .38) [6]. G-power software [17] indicated that a sample of 39 caregivers would be needed to detect a similar effect (setting power at .80 and alpha at .05) using correlation analyses.…”
Section: Power Analysismentioning
confidence: 98%
“…HNC caregivers report higher levels of perceived burden and strain at 2-6 months post-diagnosis, compared to later in the disease trajectory [11]. Only one study has identified factors that are associated with the experience of PTSD symptoms in HNC caregivers, and this found that depression and anxiety, as well as perceptions of disease threat, were associated with a greater number of symptoms [6].…”
Section: Introductionmentioning
confidence: 97%
“…Caregivers of patients with HNC also report low mood and fear of cancer recurrence [5]. Moreover, recent research has established that spouses of patients with HNC report high levels of posttraumatic stress disorder (PTSD) symptoms at diagnosis [6]. Twenty-nine percent of spouses met criteria for estimated PTSD caseness in comparison to 11 % of patients.…”
This preliminary study suggests that caregivers who have perceptions of low benefits from treatment and many patient symptoms, and those using avoidant coping strategies, are at increased risk of experiencing symptoms of PTSD. Psychological interventions that target illness perceptions and coping may help to reduce the prevalence of PTSD in caregivers of patients with HNC.
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Caregivers of acute leukemia patients had significantly more severe PTSS than did their patients. This study is the first to investigate PTSS among family caregivers of adult patients with acute leukemia and its related factors in a matched sample. More attention should be paid to the caregivers of patients with acute leukemia to minimize their PTSS and thus improve mental health of caregivers and reduce potential negative consequences for the patients themselves.
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