De La Riva, 19579 | 34/4–14 Open Case series | Various | ACTH/ cortisone | None Relatives’ reports and psychiatric assessments | 61% of sample had psychiatric SE: 59% “depressive”, 41% “euphoric” Depressed group had usually shown euphoric symptoms first | No standardised tests used Little detail given about nature of psychiatric SE |
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Harris, 198630 | 16/4–16 Prospective Child as own control Repeated measures | ALL (14) Lymphoma (2) | Prednisolone (pred) 40–60 mg/day oral for 4/52 every 4/12 | CSI CDI SHSQ | Night-waking increased on pred (NS). Irritability, tearfulness, argumentativeness, mild depressive symptoms and tiredness increased when on pred | CDI is for use in children over 8 y of age, excluding 6 of their sample. Not blinded |
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Suess, 198622 | 120/9–18 Prospective Comparison Single blind | Asthma | Non-asthmatic controls v theophylline only v theoph + pred (alt days 16 mg/day) | BVRT WMS | Increased delayed memory recall in steroid groups at 6–8 h. No significant difference between groups at 22–24 h or 46–48 h post-dose | No steroid alone group so ? differences due to steroid- theophylline interaction |
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Bender, 198831 | 27/8–16 Prospective Comparison HD v LD | Asthma | Prednisolone (oral) 3.3 mg/day (low dose, LD) v 62 mg/day (high dose, HD) | CDI, CMAS, CPT, DRT, SRT, ultrasonic motion detector for hyperactivity, static steadiness tester for fine motor control | HD: decreased memory, increased anxiety + depressive symptoms. No differences in impulsiveness, hyperactivity, motor unsteadiness | No information gathered from parents/carers. Children not asked re other psychiatric Sx |
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Bender, 199132 | 32/8–16 Prospective Comparison HD v LD | Asthma | Prednisolone (oral) 7 mg/day (LD) v 62 mg/day (HD) | PPVT, CGAS, FGAS, CDI, CMAS, CPT, SRT, ultrasonic motion detector for hyperactivity, static steadiness tester for fine motor control | Confirmed above results No predisposing factors identified | Children not asked re other psychiatric Sx. ? Atypical sample in terms of social class |
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Nall 199229 | 19/7–15 Prospective Child as own control | Asthma | Prednisolone (oral) 1–2 mg/kg/day on or off | WRAT-R BRP-2 | No difference in cognitive tests or behaviour scale score | Researchers not blind |
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Drigan, 199233 | 38/2.5–8.8 Prospective Comparison Repeated measures | ALL | Chemo + pred (oral) 40 mg/m2/day (Ch+LD) v chem + pred 120 mg/m2/day (Ch+HD) v chemo alone | Conners Parent-Teacher Hyperkinesis Index (amended) administered to parents only | Adverse changes in attention/hyperactivity, emotionality, sleep disturbance, depressed mood, listlessness + peer relations in Ch+LD and Ch+HD v Ch alone No differences in behaviours between Ch+HD v Ch+LD | Small matched sample size may have limited ability to detect difference between LD and HD groups |
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Bender, 199821 | 102/6–17 Prospective Double-blind controlled multi-centre | Asthma | Beclomethasone (inh) 2×50 μg qds+placebo tab v theophylline+placebo inhaler | CBCL, WISC-R, W-J, SCWT, WCST, TT, BRVRT, SDLT, RAVLT | No significant differences in cognitive tests or behaviour between groups | Sample did not include children under 6 who may be most vulnerable to APSE from inhaled steroids |
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Klein-Gitelman, 199811 | 213/1–18 Case series | Acute rheumatic disease | Intermittent pulsed IV methylprednisolone 30 mg/kg | None | 10% of sample had adverse psychological SE, including psychosis. Majority appeared post pulse and ceased within 48 h | Case series rather than controlled study |
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Soliday, 199928 | 10/ages not known Prospective Child as own control | Steroid sensitive idiopathic nephritic syndrome | “High dose” prednisolone therapy (oral) | CBCL | Anxious, depressive and aggressive behavioural changes at doses of >1 mg/kg/48 h | Small sample Not blinded |