Volume 32, Issue 10 pp. 737-743
Research Article

LONG-TERM OUTCOME IN PEDIATRIC TRICHOTILLOMANIA

Maya C. Schumer

Maya C. Schumer

Yale Child Study Center, New Haven, Connecticut

Both authors contributed equally to this work.

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Kaitlyn E. Panza M.A.

Kaitlyn E. Panza M.A.

Arizona State University

Both authors contributed equally to this work.

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Jilian M. Mulqueen B.A.

Jilian M. Mulqueen B.A.

Yale Child Study Center, New Haven, Connecticut

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Ewgeni Jakubovski M.A.

Ewgeni Jakubovski M.A.

Yale Child Study Center, New Haven, Connecticut

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Michael H. Bloch M.D., M.S.

Corresponding Author

Michael H. Bloch M.D., M.S.

Yale Child Study Center, New Haven, Connecticut

Department of Psychiatry, Yale University, New Haven, Connecticut

Correspondence to: Michael H. Bloch, Child Study Center, Yale University School of Medicine, PO Box 207900, New Haven, CT 06520. E-mail: [email protected]Search for more papers by this author
First published: 02 July 2015
Citations: 25

Contract grant sponsor: National Center for Research Resources; Contract grant number: UL1 RR024139.

Trial Registry Name: clinicaltrials.gov

Registry identification number: NCT00993265

Abstract

Objective

To examine long-term outcome in children with trichotillomania.

Method

We conducted follow-up clinical assessments an average of 2.8 ± 0.8 years after baseline evaluation in 30 of 39 children who previously participated in a randomized, double-blind, placebo-controlled trial of N-acetylcysteine (NAC) for pediatric trichotillomania. Our primary outcome was change in hairpulling severity on the Massachusetts General HospitalHairpulling Hospital Hairpulling Scale (MGH-HPS) between the end of the acute phase and follow-up evaluation. We also obtained secondary measures examining styles of hairpulling, comorbid anxiety and depressive symptoms, as well as continued treatment utilization. We examined both correlates and predictors of outcome (change in MGH-HPS score) using linear regression.

Results

None of the participants continued to take NAC at the time of follow-up assessment. No significant changes in hairpulling severity were reported over the follow-up period. Subjects reported significantly increased anxiety and depressive symptoms but improvement in automatic pulling symptoms. Increased hairpulling symptoms during the follow-up period were associated with increased depression and anxiety symptoms and increased focused pulling. Older age and greater focused pulling at baseline assessment were associated with poor long-term prognosis.

Conclusions

Our findings suggest that few children with trichotillomania experience a significant improvement in trichotillomania symptoms if behavioral treatments are inaccessible or have failed to produce adequate symptom relief. Our findings also confirm results of previous cross-sectional studies that suggest an increased risk of depression and anxiety symptoms with age in pediatric trichotillomania. Increased focused pulling and older age among children with trichotillomania symptoms may be associated with poorer long-term prognosis.

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