Clinical presentation of postnatal and non-postnatal depressive episodes

2007 ◽  
Vol 37 (9) ◽  
pp. 1273-1280 ◽  
Author(s):  
CARLY COOPER ◽  
LISA JONES ◽  
EMMA DUNN ◽  
LIZ FORTY ◽  
SAYEED HAQUE ◽  
...  

ABSTRACTBackgroundThe relationship of postnatal (postpartum) depression (PND) to episodes of depression occurring at other times is not well understood. Despite a number of studies of clinical presentation, there is little consistency in the literature. We have undertaken within- and between-individual comparisons of the clinical presentation of postnatal (PN) and non-postnatal (NPN) depressive episodes in women with recurrent depression.MethodIn a sample of well-characterized, parous women meeting DSM-IV and ICD-10 criteria for recurrent major depressive disorder, the clinical presentation of episodes of major depression with onset within 4 weeks of giving birth (PND group, n=50) were compared with (i) the non-postnatal episodes of women with PND, and (ii) episodes of major depression in parous women who had not experienced episodes of mood disorder in relation to childbirth (NPND group, n=132). In addition, the non-postnatal episodes of the PND group of women were compared with the depressive episodes of the NPND group.ResultsThe small number of differences found between PN and NPN depressive episodes, such as reduced early morning wakening in postnatal episodes, are likely to be explicable by the context of having a new baby rather than by any difference in the nature of the underlying depression.ConclusionsThe results do not point to substantial differences in clinical presentation between episodes of major depression occurring in relation to childbirth and at other times. Other avenues of research are therefore required to demonstrate a specific relationship between childbirth and depression.

2014 ◽  
Author(s):  
Jose Gonzalez ◽  
Samantha Russell ◽  
Brooke Edwards ◽  
Cassie Padilla ◽  
Aned Bosques ◽  
...  

1990 ◽  
Vol 5 (1) ◽  
pp. 29-30
Author(s):  
F Lang ◽  
J Pellet ◽  
B Estour

SummaryThe authors report the case of a 45-yr-old male who presented from 1979 to 1986 with several severe depressive episodes. The patient fulfilled Feighner criteria for major depression, Newcastle criteria for endogenous depression: the depressive episodes were all classified as severe recurrent depression without melancholia according to DSM III. The patient was resistant to different types of treatment (ECT, tricyclic and MAOI drugs, lithium, sleep deprivation). With a treatment of 10 cg/day of fenetyline, reduced to 5 cg/day after 6 months, (atypical manic episode), the patient improved considerably for 20 rnonths. The therapeutic response decreased after this period but after a month of withdrawal, the patient again responded. The authors cannot explain the duration of this therapeutic response.


2008 ◽  
Vol 113 (6) ◽  
pp. 427-438 ◽  
Author(s):  
Susan W. Harris ◽  
David Hessl ◽  
Beth Goodlin-Jones ◽  
Jessica Ferranti ◽  
Susan Bacalman ◽  
...  

Abstract Autism, which is common in individuals with fragile X syndrome, is often difficult to diagnose. We compared the diagnostic classifications of two measures for autism diagnosis, the ADOS and the ADI-R, in addition to the DSM-IV-TR in 63 males with this syndrome. Overall, 30% of the subjects met criteria for autistic disorder and 30% met criteria for PDD-NOS. The classifications on the ADOS and DSM-IV-TR were most similar, whereas the ADI-R classified subjects as autistic much more frequently. We further investigated the relationship of both FMRP and FMR1 mRNA to symptoms of autism in this cohort and found no significant relationship between the measures of autism and molecular features, including FMRP, FMR1 mRNA, and CGG repeat number.


1992 ◽  
Vol 180 (8) ◽  
pp. 491-497 ◽  
Author(s):  
MARY ELLEN McNAUGHTON ◽  
THOMAS L. PATTERSON ◽  
MICHAEL R. IRWIN ◽  
IGOR GRANT

Children ◽  
2020 ◽  
Vol 7 (7) ◽  
pp. 69 ◽  
Author(s):  
Natasha A. Nakra ◽  
Dean A. Blumberg ◽  
Angel Herrera-Guerra ◽  
Satyan Lakshminrusimha

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection may result in the multisystem inflammatory syndrome in children (MIS-C). The clinical presentation of MIS-C includes fever, severe illness, and the involvement of two or more organ systems, in combination with laboratory evidence of inflammation and laboratory or epidemiologic evidence of SARS-CoV-2 infection. Some features of MIS-C resemble Kawasaki Disease, toxic shock syndrome, and secondary hemophagocytic lymphohistiocytosis/macrophage activation syndrome. The relationship of MIS-C to SARS-CoV-2 infection suggests that the pathogenesis involves post-infectious immune dysregulation. Patients with MIS-C should ideally be managed in a pediatric intensive care environment since rapid clinical deterioration may occur. Specific immunomodulatory therapy depends on the clinical presentation. The relationship between the immune response to SARS-CoV-2 vaccines in development and MIS-C requires further study.


2010 ◽  
Vol 108 (1-2) ◽  
pp. 141-145 ◽  
Author(s):  
Attila J. Pulay ◽  
Frederick S. Stinson ◽  
W. June Ruan ◽  
Sharon M. Smith ◽  
Roger P. Pickering ◽  
...  

2015 ◽  
Vol 226 (1) ◽  
pp. 273-276 ◽  
Author(s):  
Donald W. Black ◽  
William Coryell ◽  
Raymond Crowe ◽  
Martha Shaw ◽  
Brett McCormick ◽  
...  

2009 ◽  
Vol 195 (6) ◽  
pp. 525-530 ◽  
Author(s):  
David A. Solomon ◽  
Andrew C. Leon ◽  
Jean Endicott ◽  
William H. Coryell ◽  
Chunshan Li ◽  
...  

BackgroundMuch remains unknown about the phenomenology of bipolar I disorder.AimsTo determine the type of bipolar I mood episodes that occur over time, and their relative frequency.MethodA total of 219 individuals with Research Diagnostic Criteria bipolar I disorder were prospectively followed for up to 25 years (median 20 years). Psychopathology was assessed with the Longitudinal Interval Follow-up Evaluation.ResultsOverall, 1208 mood episodes were prospectively observed. The episodes were empirically classified as follows: major depression, 30.9% (n = 373); minor depression, 13.0% (n = 157); mania, 20.4% (n = 246); hypomania, 10.4% (n = 126); cycling, 17.3% (n = 210); cycling plus mixed state, 7.8% (n = 94); and mixed, 0.2% (n = 2).ConclusionsCycling episodes constituted 25% of all episodes. Work groups revising ICD–10 and DSM–IV should add a category for bipolar I cycling episode.


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