TY - JOUR
T1 - Features associated with the delayed initiation of mood stabilizers at illness onset in bipolar disorder
AU - Goldberg, Joseph F.
AU - Ernst, Carrie L.
PY - 2002/11
Y1 - 2002/11
N2 - Background: Whether delays in the initiation of appropriate pharmacotherapy for bipolar illness negatively affect course, outcome, or lifetime suicide risk remains at issue. Method: Lifetime affective syndromes and the initial emergence of affective symptoms were assessed by lifecharting in 56 DSM-IV bipolar patients. Lifetime treatment interventions were recorded by clinical interview with corroboration via record reviews. Lag times to the initiation of a mood stabilizer (after initial symptom onset and/or first lifetime affective episode) were assessed relative to functional outcome and lifetime suicide attempts. Results: Mean ± SD lag time from initial affective symptoms until first mood stabilizer treatment was 9.8 ± 9.4 years. A greater number of years from symptom onset to first mood stabilizer was associated with poorer past year social functioning (r = -0.35, p = .008), more annual hospitalizations (r = 0.38, p = .004), and a greater likelihood for making a lifetime suicide attempt (odds ratio = 7.26, 95% confidence interval = 1.62 to 32.59; Wald χ2 = 6.69, df = 1, p = .010). Delayed mood stabilizer initiation was linked with poorer outcomes in these domains regardless of initial index episode polarities of mania versus depression. Prolonged delays to bipolar diagnoses and mood stabilizer initiation were associated with earlier ages at affective symptom onset (p < .03) and milder severity of initial symptoms (p = .003). Psychotherapy initiation often preceded mood stabilizer introduction by ≥ 8 years. Conclusion: Delays in the initiation of mood stabilizer pharmacotherapy at illness onset, even for relatively mild symptoms at illness onset and regardless of index episode polarity, may confer an elevated risk for suicidal behavior, poorer social adjustment, and more hospitalizations in bipolar disorder. Greater surveillance screening for bipolar illness in patients who first present for psychotherapy may help to diminish these adverse outcomes.
AB - Background: Whether delays in the initiation of appropriate pharmacotherapy for bipolar illness negatively affect course, outcome, or lifetime suicide risk remains at issue. Method: Lifetime affective syndromes and the initial emergence of affective symptoms were assessed by lifecharting in 56 DSM-IV bipolar patients. Lifetime treatment interventions were recorded by clinical interview with corroboration via record reviews. Lag times to the initiation of a mood stabilizer (after initial symptom onset and/or first lifetime affective episode) were assessed relative to functional outcome and lifetime suicide attempts. Results: Mean ± SD lag time from initial affective symptoms until first mood stabilizer treatment was 9.8 ± 9.4 years. A greater number of years from symptom onset to first mood stabilizer was associated with poorer past year social functioning (r = -0.35, p = .008), more annual hospitalizations (r = 0.38, p = .004), and a greater likelihood for making a lifetime suicide attempt (odds ratio = 7.26, 95% confidence interval = 1.62 to 32.59; Wald χ2 = 6.69, df = 1, p = .010). Delayed mood stabilizer initiation was linked with poorer outcomes in these domains regardless of initial index episode polarities of mania versus depression. Prolonged delays to bipolar diagnoses and mood stabilizer initiation were associated with earlier ages at affective symptom onset (p < .03) and milder severity of initial symptoms (p = .003). Psychotherapy initiation often preceded mood stabilizer introduction by ≥ 8 years. Conclusion: Delays in the initiation of mood stabilizer pharmacotherapy at illness onset, even for relatively mild symptoms at illness onset and regardless of index episode polarity, may confer an elevated risk for suicidal behavior, poorer social adjustment, and more hospitalizations in bipolar disorder. Greater surveillance screening for bipolar illness in patients who first present for psychotherapy may help to diminish these adverse outcomes.
UR - http://www.scopus.com/inward/record.url?scp=0036854298&partnerID=8YFLogxK
U2 - 10.4088/JCP.v63n1105
DO - 10.4088/JCP.v63n1105
M3 - Article
C2 - 12444811
AN - SCOPUS:0036854298
SN - 0160-6689
VL - 63
SP - 985
EP - 991
JO - Journal of Clinical Psychiatry
JF - Journal of Clinical Psychiatry
IS - 11
ER -