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Fluctuation of Catatonic Signs in a Naturalistic Clinical Sample
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Background
We are unaware of investigations into whether catatonic signs fluctuate over short periods, so we quantified changes in catatonic signs over 24-hours in a naturalistic clinical sample.
Methods
Psychiatric inpatients with catatonia were evaluated using the Bush Francis Catatonia Rating Scale (BFCRS) during morning rounds (t
1
), at approximately 5-6 p.m. (t
2
), and the following day’s rounds (t
3
). Descriptive statistics were calculated regarding changes in sign presence/absence, severity, and laterality, as well as catatonic caseness.
Results
Twenty-six patients were included, and 19.2% (5/26) were not treated for catatonia using GABA (gamma-aminobutyric acid)-ergic agents, NMDA (N-methyl-D-aspartate)-receptor antagonists, or electroconvulsive therapy from t
1
to t
3
. All patients experienced at least one of the following for at least one catatonic sign from t
1
to t
3
: disappearance, emergence, laterality change, or severity change. Among untreated patients from t
1
to t
3
, BFCRS scores were higher at t
1
and t
3
than t
2
, suggesting catatonia may be more severe in the morning. Where BFCRS scores were available for all timepoints, 8.3% (2/24) of patients lost caseness at t
2
and regained it at t
3
, including 20.0% (1/5) of untreated patients.
Conclusion
These data suggest catatonic signs fluctuate over short periods, and catatonic caseness may be lost and regained over 24 h.
Title: Fluctuation of Catatonic Signs in a Naturalistic Clinical Sample
Description:
Background
We are unaware of investigations into whether catatonic signs fluctuate over short periods, so we quantified changes in catatonic signs over 24-hours in a naturalistic clinical sample.
Methods
Psychiatric inpatients with catatonia were evaluated using the Bush Francis Catatonia Rating Scale (BFCRS) during morning rounds (t
1
), at approximately 5-6 p.
m.
(t
2
), and the following day’s rounds (t
3
).
Descriptive statistics were calculated regarding changes in sign presence/absence, severity, and laterality, as well as catatonic caseness.
Results
Twenty-six patients were included, and 19.
2% (5/26) were not treated for catatonia using GABA (gamma-aminobutyric acid)-ergic agents, NMDA (N-methyl-D-aspartate)-receptor antagonists, or electroconvulsive therapy from t
1
to t
3
.
All patients experienced at least one of the following for at least one catatonic sign from t
1
to t
3
: disappearance, emergence, laterality change, or severity change.
Among untreated patients from t
1
to t
3
, BFCRS scores were higher at t
1
and t
3
than t
2
, suggesting catatonia may be more severe in the morning.
Where BFCRS scores were available for all timepoints, 8.
3% (2/24) of patients lost caseness at t
2
and regained it at t
3
, including 20.
0% (1/5) of untreated patients.
Conclusion
These data suggest catatonic signs fluctuate over short periods, and catatonic caseness may be lost and regained over 24 h.
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