Depression and post-traumatic stress disorder after aneurysmal subarachnoid haemorrhage in relation to lifetime psychiatric morbidity
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作者:
Hedlund, Mathilde
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Uppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, Sweden
Karolinska Inst, Dept Neurobiol Care Sci & Soc, Stockholm, SwedenUppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, Sweden
Hedlund, Mathilde
[1
,2
]
Zetterling, Maria
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Uppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, SwedenUppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, Sweden
Zetterling, Maria
[1
]
Ronne-Engstrom, Elisabeth
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Uppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, SwedenUppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, Sweden
Ronne-Engstrom, Elisabeth
[1
]
Carlsson, Marianne
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Uppsala Univ, Dept Publ Hlth & Caring Sci, SE-75185 Uppsala, SwedenUppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, Sweden
Carlsson, Marianne
[3
]
Ekselius, Lisa
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Uppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, SwedenUppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, Sweden
Ekselius, Lisa
[1
]
机构:
[1] Uppsala Univ, Univ Uppsala Hosp, Dept Neurosci, SE-75185 Uppsala, Sweden
[2] Karolinska Inst, Dept Neurobiol Care Sci & Soc, Stockholm, Sweden
[3] Uppsala Univ, Dept Publ Hlth & Caring Sci, SE-75185 Uppsala, Sweden
Introduction. Little is known about the roles that lifetime psychiatric disorders play in psychiatric and vocational outcomes of aneurysmal subarachnoid haemorrhage (SAH). Materials and methods. Eighty-three SAH patients without apparent cognitive dysfunction were assessed using the Structured Clinical Interview for DSM-IV axis I disorders (SCID-I) after their SAH. Diagnoses were assessed for three time periods, 'lifetime before SAH', '12 months before SAH' and '7 months after SAH'. Results. Forty-five percentage of patients with SAH reported at least one lifetime psychiatric disorder. After SAH, symptoms of depression and/or post-traumatic stress disorder (PTSD) were seen in 41%, more often in those with a psychiatric history prior to SAH (p = 0.001). In logistic regressions, depression after SAH was associated with a lifetime history of major depression, or of anxiety or substance use disorder, as well as with lifetime psychiatric comorbidity. Subsyndromal or full PTSD was predicted by a lifetime history of major depression. After the SAH, 18 patients (22%) had received psychotropic medication and/or psychological treatment, 13 of whom had a disorder. Those with a lifetime history of major depression or treatment with antidepressants before SAH had lower return to work rates than others (p = 0.019 and p = 0.031, respectively). This was also true for those with symptoms of depression and/or PTSD, or with antidepressant treatment after SAH (p = 0.001 and p = 0.031, respectively). Conclusions. Depression and PTSD are present in a substantial proportion of patients 7 months after SAH. Those with a history of psychiatric morbidity, any time before the SAH, are more at risk and also constitute a risk group for difficulties in returning to work.
机构:
Univ Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Royal Prince Alfred Hosp, Sydney, NSW, AustraliaUniv Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Glozier, Nick
;
Hackett, Maree L.
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Univ Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Royal Prince Alfred Hosp, Sydney, NSW, Australia
Univ Auckland, Fac Med & Hlth Sci, Sch Populat Hlth, Clin Trial Res Unit, Auckland 1, New ZealandUniv Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Hackett, Maree L.
;
Parag, Varsha
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Univ Auckland, Fac Med & Hlth Sci, Sch Populat Hlth, Clin Trial Res Unit, Auckland 1, New ZealandUniv Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Parag, Varsha
;
Anderson, Craig S.
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机构:
Univ Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Royal Prince Alfred Hosp, Sydney, NSW, Australia
Univ Auckland, Fac Med & Hlth Sci, Sch Populat Hlth, Clin Trial Res Unit, Auckland 1, New ZealandUniv Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
机构:
Univ Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Royal Prince Alfred Hosp, Sydney, NSW, AustraliaUniv Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Glozier, Nick
;
Hackett, Maree L.
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h-index: 0
机构:
Univ Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Royal Prince Alfred Hosp, Sydney, NSW, Australia
Univ Auckland, Fac Med & Hlth Sci, Sch Populat Hlth, Clin Trial Res Unit, Auckland 1, New ZealandUniv Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Hackett, Maree L.
;
Parag, Varsha
论文数: 0引用数: 0
h-index: 0
机构:
Univ Auckland, Fac Med & Hlth Sci, Sch Populat Hlth, Clin Trial Res Unit, Auckland 1, New ZealandUniv Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Parag, Varsha
;
Anderson, Craig S.
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h-index: 0
机构:
Univ Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia
Royal Prince Alfred Hosp, Sydney, NSW, Australia
Univ Auckland, Fac Med & Hlth Sci, Sch Populat Hlth, Clin Trial Res Unit, Auckland 1, New ZealandUniv Sydney, George Inst Int Hlth, Sydney, NSW 2050, Australia