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Authors' reply

Published online by Cambridge University Press:  02 January 2018

Lars Vedel Kessing
Affiliation:
Psychiatric Center Copenhagen, Department O and Faculty of Health and Medical Sciences, University of Copenhagen
Per Kragh Andersen
Affiliation:
Department of Biostatistics, University of Copenhagen, Denmark. Email: Lars.Vedel.Kessing@regionh.dk
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Abstract

Type
Columns
Copyright
Copyright © Royal College of Psychiatrists, 2014 

We are confident that the relatively low response rates to lithium in our study relate to the narrow definition of lithium response, rather than to characteristics of the included patients. Reference Kessing, Vradi and Andersen1 Thus, we intended to characterise patients who had an excellent response to lithium monotherapy; that is, patients who were ‘cured’ from further affective episodes following a start-up period of lithium as in a prior study. Reference Kessing, Hellmund and Andersen2 We used two robust clinical indicators to define excellent lithium response: (a) lithium prescribed in monotherapy; and (b) no need for psychiatric hospital admission. By doing this, we defined lithium response in a rather rigorous way, resulting in relatively low rates of response. We do not find that our definition of lithium response hampered the finding of the study that early treatment with lithium was associated with increased probability of excellent lithium response compared with delayed treatment, or hampered the generalisability of this finding. Although cycle acceleration occurs on average in bipolar disorder Reference Kessing, Hansen and Andersen3,Reference Kessing, Olsen and Andersen4 the results of our study may suggest that early treatment with lithium might prevent progression of bipolar disorder.

References

1 Kessing, LV Vradi, E Andersen, PK Starting lithium prophylaxis early v. late in bipolar disorder. Br J Psychiatry 2014; 205: 214–20.Google ScholarPubMed
2 Kessing, LV Hellmund, G Andersen, PK Predictors of excellent response to lithium: results from a nationwide register-based study. Int Clin Psychopharmacol 2011; 26: 323–8.CrossRefGoogle ScholarPubMed
3 Kessing, LV Hansen, MG Andersen, PK Course of illness in depressive and bipolar disorders. Naturalistic study, 1994–1999. Br J Psychiatry 2004; 185: 372–7.CrossRefGoogle ScholarPubMed
4 Kessing, LV Olsen, EW Andersen, PK Recurrence in affective disorder: analyses with frailty models. Am J Epidemiol 1999; 149: 404–11.CrossRefGoogle ScholarPubMed
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