Functional outcome in childhood-onset schizophrenia in
Nigeria: a 3-year longitudinal study
Musa U. Umar, Shehu Sale
Department of Psychiatry, Child and
Adolescent Mental Health Unit, Aminu Kano
Teaching Hospital, Bayero University, Kano,
Nigeria
Correspondence to Musa Usman Umar, MBBS,
FWACP, Department of Psychiatry, Child and
Adolescent Mental Health Unit, Aminu Kano
Teaching Hospital, Bayero University, Zaria
Road, PMB 3452, 77189 UNIBAYERO NG,
Kano, Nigeria, Tel: +234 803 660 5552;
e-mail: sophiee87@yahoo.com
Received 11 February 2016
Accepted 1 May 2016
Egyptian Journal of Psychiatry
2016, 37:118–124
Background
The outcome of childhood-onset schizophrenia (COS) is generally regarded as
poor. Few prospective studies have been reported from developing countries.
Aim
The aim of the present study was to assess the functional outcome in COS and the
factors associated with poor outcome.
Methods
This 3-year prospective study included 19 patients with COS. Diagnosis was based
on the Diagnostic and Statistical Manual of Mental Disorders, 4th ed., criteria using
the Kiddie-Schedule for Affective Disorders and Schizophrenia - Present and
Lifetime Version; severity was assessed through the Positive and Negative
Symptoms Scale, whereas the measure of outcome used was Children’s Global
Assessment Scale.
Results
The mean duration of follow-up was 39.53 (SD ±5.37) months. The mean age of onset
of COS was 10.47 (SD ±0.91) years. At the end of the study, 31.6% of the participants
had good outcome, 42.1% had moderate outcome, and 26.3% had poor outcome.
Factors associated with poor outcome included history of perinatal complication, more
negative symptoms, and longer duration of untreated psychosis.
Conclusion
More than a third of the sample showed good outcome over the few years of follow-
up. On the basis of the findings of this study, we recommend an early intervention.
Keywords:
childhood-onset schizophrenia, functional outcome, prospective follow-up study
Egypt J Psychiatr 37:118–124
© 2016 Egyptian Journal of Psychiatry
1110-1105
Introduction
Schizophrenia most commonly emerges during late
teens and early adulthood, but it can also be
diagnosed during childhood (American Psychiatric
Association, 2013). Childhood-onset schizophrenia
(COS) is a severe form of psychotic disorder that
occurs at the age of 13 years or younger and is often
chronic and persistently debilitating (Remschmidt
et al., 2007). It is a severe form of the late
adolescent and early adult-onset disorder (Rapoport
and Inoff-Germain, 2000).
COS is a rare disorder; in preadolescents, the estimated
prevalence is less than one case per 10 000 (Asarnow
et al., 2004). The number of new cases significantly
increase during late adolescence, reaching an
approximate prevalence of 1% for later-onset
schizophrenia. It occurs more in males unlike the
adult-onset type that has equal ratio.
Individuals with COS present with more premorbid
impairment than do those with late-onset, with an
increased prevalence of genetic abnormalities
(Addington and Rapoport, 2009). A clinical and
outcome study by Hassan and Taha (2011) reported
that about 24% of patients with early-onset
schizophrenia had good outcome, and that premorbid
adjustment, intelligence quotient, negative symptoms,
and gradual onset were associated with poor outcome. In
a recent systematic review, good outcome for early-onset
schizophrenia was 15.4%, with male sex and longer
follow-up periods as predictors of poor outcome
(Clemmensen et al., 2012). Most studies around the
world have reported poor prognosis for COS (Jarbin and
von Knorring, 2003; Gonthier and Lyon, 2004; Röpcke
and Eggers, 2005; Remschmidt et al., 2007), although a
recent meta-analysis reported better outcome in patients
with early-onset schizophrenia compared with the adult-
onset group (Amminger et al., 2011).
Because COS is a rare disorder, it is poorly understood
and has not received adequate attention from researchers
(Bartlett, 2004; Clemmensen et al., 2012). It is
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118 Original article
© 2016 Egyptian Journal of Psychiatry | Published by Wolters Kluwer - Medknow DOI: 10.4103/1110-1105.195549
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