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Dive into the research topics where Ralph J. Koek is active.

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Featured researches published by Ralph J. Koek.


Acta Psychiatrica Scandinavica | 2004

Antidepressants and suicidal behaviour in unipolar depression

Boghos I. Yerevanian; Ralph J. Koek; Jamie D. Feusner; S. Hwang; Jim Mintz

Objective:  To compare the rates of suicidal behaviour during vs. after discontinuation of treatment with antidepressants, and to determine the comparative rates of suicidal behaviour for patients maintained on tricyclic (TCA) vs. selective serotonin reuptake inhibitor (SSRI) antidepressants.


Journal of Affective Disorders | 1999

Hemispheric asymmetry in depression and mania : A longitudinal QEEG study in bipolar disorder

Ralph J. Koek; Boghos I. Yerevanian; Kenneth Tachiki; James C. Smith; Joseph Alcock; Alex Kopelowicz

BACKGROUND previous research has been inconclusive about the nature of hemispheric asymmetry in emotional processing. METHOD 13 patients with DSM-IV bipolar disorder received repeated QEEGs over 2 years in different mood states. Z-score measures of asymmetry were assessed. RESULTS asymmetry in frontotemporal slow-wave activity appeared to be in opposite directions in depression compared to mania/hypomania. CONCLUSIONS mood change in bipolar disorder is associated with change in QEEG asymmetry. LIMITATIONS study of larger numbers of more homogenous patients under similar conditions is needed. CLINICAL RELEVANCE study of mood state-dependent asymmetry changes in bipolar disorder may lead to better understanding of hemispheric processing of emotion.


Journal of Affective Disorders | 2001

Anxiety disorders comorbidity in mood disorder subgroups: data from a mood disorders clinic.

Boghos I. Yerevanian; Ralph J. Koek; Swarnalatha Ramdev

BACKGROUND Previous research has identified a high rate of anxiety disorders comorbidity in patients with a primary mood disorder diagnosis. Discrepancies between studies in the comorbidity prevalence of specific anxiety disorders in mood disorders, and of anxiety disorders comorbidity between unipolar depression and bipolar mood disorder are in part due to differences in sampling and diagnostic assessment methodology. METHOD The authors reviewed the charts of 138 patients who received the SCID-P for DSM-III on enrollment in a Mood Disorders Clinic during the period 1982 through 1988. The comorbidity of specific DSM-III Anxiety Disorders with specific mood disorders was determined and comparatively examined using non-parametric statistics. RESULTS There was high overall comorbidity of anxiety disorders that did not differ between bipolar and unipolar subjects. There were no differences in the comorbidity of individual anxiety disorder diagnoses in the unipolar vs. bipolar groups. However, in unipolar patients with, compared to those without an additional diagnosis of dysthymia, there was greater overall anxiety disorders comorbidity, with a particularly high prevalence of generalized anxiety disorder. LIMITATION The subgroup of patients with bipolar I disorder was relatively small (N=8). CONCLUSION Mood and anxiety disorders comorbidity is complex and presents a continuing challenge for both clinicians and researchers.


Progress in Neuro-psychopharmacology & Biological Psychiatry | 2016

Treatment-refractory posttraumatic stress disorder (TRPTSD): a review and framework for the future☆

Ralph J. Koek; Holly N. Schwartz; Stephenie Scully; Jean-Philippe Langevin; Shana Spangler; Arkady Korotinsky; Kevin Jou; Andrew F. Leuchter

Post-traumatic stress disorder (PTSD) is a serious psychiatric consequence of trauma that occurs in a proportion of individuals exposed to life-threatening events. Trauma-focused psychotherapy is often recommended as first choice for those who do not recover spontaneously. But many individuals require medications. In the US, only paroxetine (PRX) and sertraline (SRT) are FDA approved for PTSD. But response and remission rates with these medications are low, so numerous other pharmacologic interventions have been tried. To date, there has not been a systematic review of the data on what are the best next-step pharmacologic strategies for individuals who fail standard treatments. To that end, we review 168 published trials of medications other than PRX or SRT and provide a detailed analysis of the 88/168 studies that describe alternative pharmacologic interventions in patients refractory to other treatment. We also review clinical factors relevant to treatment-refractory PTSD; the neurobiology of extinction, as well as evidence-based psychotherapy and neuromodulation strategies for this condition.


Journal of Affective Disorders | 2012

Subtypes of antipsychotics and suicidal behavior in bipolar disorder

Ralph J. Koek; Boghos I. Yerevanian; Jim Mintz

OBJECTIVE Antipsychotics are commonly used in bipolar disorder, with newer (SGA) agents increasingly replacing FGA antipsychotics, particularly in bipolar depression. There are few data on differences between FGA and SGA antipsychotics in terms of their relationship to suicidal behavior in bipolar disorder. METHOD This was a retrospective chart review of 161 bipolar veterans treated naturalistically with antipsychotics at a university-affiliated VA hospital and clinics for up to 8 years. Charts were reviewed to determine monthly antipsychotic use and occurrence of suicidal behavior: completed suicide, attempted suicide or hospitalization to prevent suicide. Suicidal behavior events were compared across patients during treatment with individual antipsychotics and FGAs or SGAs as a class. RESULTS Non-lethal suicide events were more common during FGA than SGA monotherapy (9 events/110 months of exposure vs. 6 events/381 months of exposure; χ(2)=9.65, p=0.002). Suicide event rates did not differ between FGAs and SGAs when used in conjunction with mood stabilizers. Event rates were lower with lithium than anticonvulsants when used in conjunction with antipsychotics. No differences were found between olanzapine, risperidone and quetiapine. LIMITATIONS The retrospective chart review methodology may have led to confounding by indication and diagnostic inaccuracy. No completed suicides occurred. Study participants were primarily male veterans. Results may not be generalizable to SGAs marketed since 2003. CONCLUSIONS FGA antipsychotic monotherapy may be associated with higher suicidal behavior risk than SGA antipsychotic monotherapy. Antipsychotics used in conjunction with mood stabilizers, particularly lithium, are associated with lower rates, independent of antipsychotic subtype.


Brain Sciences | 2016

Deep Brain Stimulation of the Basolateral Amygdala: Targeting Technique and Electrodiagnostic Findings

Jean-Philippe Langevin; James W. Y. Chen; Ralph J. Koek; David L. Sultzer; M. Mandelkern; Holly N. Schwartz; Scott E. Krahl

The amygdala plays a critical role in emotion regulation. It could prove to be an effective neuromodulation target in the treatment of psychiatric conditions characterized by failure of extinction. We aim to describe our targeting technique, and intra-operative and post-operative electrodiagnostic findings associated with the placement of deep brain stimulation (DBS) electrodes in the amygdala. We used a transfrontal approach to implant DBS electrodes in the basolateral nucleus of the amygdala (BLn) of a patient suffering from severe post-traumatic stress disorder. We used microelectrode recording (MER) and awake intra-operative neurostimulation to assist with the placement. Post-operatively, the patient underwent monthly surveillance electroencephalograms (EEG). MER predicted the trajectory of the electrode through the amygdala. The right BLn showed a higher spike frequency than the left BLn. Intra-operative neurostimulation of the BLn elicited pleasant memories. The monthly EEG showed the presence of more sleep patterns over time with DBS. BLn DBS electrodes can be placed using a transfrontal approach. MER can predict the trajectory of the electrode in the amygdala and it may reflect the BLn neuronal activity underlying post-traumatic stress disorder PTSD. The EEG findings may underscore the reduction in anxiety.


American Journal on Addictions | 2015

Mania following use of ibogaine: A case series.

Cole J. Marta; Wesley C. Ryan; Alex Kopelowicz; Ralph J. Koek

BACKGROUND Ibogaine is a naturally occurring hallucinogen with postulated anti-addictive qualities. While illegal domestically, a growing number of individuals have sought it out for treatment of opiate dependence, primarily in poorly regulated overseas clinics. Existing serious adverse events include cardiac and vestibular toxicity, though ours is the first report of mania stemming from its use. OBJECTIVES To report on a case series of psychiatric emergency room patients whose unregulated use of ibogaine resulted in mania in three patients with no prior diagnosis of bipolar illness. METHODS Review and summarize charts of three cases. Relevant literature was also reviewed for discussion. RESULTS Two cases of reported ibogaine ingestion for self-treatment of addictions, and one for psycho-spiritual experimentation resulted in symptoms consistent with mania. No prior reports of mania were found in the literature, and the literature suggests growing popularity of ibogaines use. CONCLUSIONS The three cases presented demonstrate a temporal association between ibogaine ingestion and subsequent development of mania. SCIENTIFIC SIGNIFICANCE In light of these cases, clinicians faced with a new onset mania may benefit from careful substance use and treatment history, specifically regarding opiates. In the vulnerable and often desperate addiction population, in particular, the number of patients seeking this treatment appears to be growing. We advise clinicians to be prepared for discussing the safety, efficacy, and paucity of good data regarding ibogaine with patients who may be considering its use. (Am J Addict 2015;24:203-205).


American Journal on Addictions | 2015

Mania following use of ibogaine: A case series: Mania Following Use of Ibogaine

Cole J. Marta; Wesley C. Ryan; Alex Kopelowicz; Ralph J. Koek

BACKGROUND Ibogaine is a naturally occurring hallucinogen with postulated anti-addictive qualities. While illegal domestically, a growing number of individuals have sought it out for treatment of opiate dependence, primarily in poorly regulated overseas clinics. Existing serious adverse events include cardiac and vestibular toxicity, though ours is the first report of mania stemming from its use. OBJECTIVES To report on a case series of psychiatric emergency room patients whose unregulated use of ibogaine resulted in mania in three patients with no prior diagnosis of bipolar illness. METHODS Review and summarize charts of three cases. Relevant literature was also reviewed for discussion. RESULTS Two cases of reported ibogaine ingestion for self-treatment of addictions, and one for psycho-spiritual experimentation resulted in symptoms consistent with mania. No prior reports of mania were found in the literature, and the literature suggests growing popularity of ibogaines use. CONCLUSIONS The three cases presented demonstrate a temporal association between ibogaine ingestion and subsequent development of mania. SCIENTIFIC SIGNIFICANCE In light of these cases, clinicians faced with a new onset mania may benefit from careful substance use and treatment history, specifically regarding opiates. In the vulnerable and often desperate addiction population, in particular, the number of patients seeking this treatment appears to be growing. We advise clinicians to be prepared for discussing the safety, efficacy, and paucity of good data regarding ibogaine with patients who may be considering its use. (Am J Addict 2015;24:203-205).


American Journal on Addictions | 2015

Mania following use of ibogaine

Cole J. Marta; Wesley C. Ryan; Alex Kopelowicz; Ralph J. Koek

BACKGROUND Ibogaine is a naturally occurring hallucinogen with postulated anti-addictive qualities. While illegal domestically, a growing number of individuals have sought it out for treatment of opiate dependence, primarily in poorly regulated overseas clinics. Existing serious adverse events include cardiac and vestibular toxicity, though ours is the first report of mania stemming from its use. OBJECTIVES To report on a case series of psychiatric emergency room patients whose unregulated use of ibogaine resulted in mania in three patients with no prior diagnosis of bipolar illness. METHODS Review and summarize charts of three cases. Relevant literature was also reviewed for discussion. RESULTS Two cases of reported ibogaine ingestion for self-treatment of addictions, and one for psycho-spiritual experimentation resulted in symptoms consistent with mania. No prior reports of mania were found in the literature, and the literature suggests growing popularity of ibogaines use. CONCLUSIONS The three cases presented demonstrate a temporal association between ibogaine ingestion and subsequent development of mania. SCIENTIFIC SIGNIFICANCE In light of these cases, clinicians faced with a new onset mania may benefit from careful substance use and treatment history, specifically regarding opiates. In the vulnerable and often desperate addiction population, in particular, the number of patients seeking this treatment appears to be growing. We advise clinicians to be prepared for discussing the safety, efficacy, and paucity of good data regarding ibogaine with patients who may be considering its use. (Am J Addict 2015;24:203-205).


Journal of Affective Disorders | 2007

Bipolar pharmacotherapy and suicidal behavior. Part I: Lithium, divalproex and carbamazepine.

Boghos I. Yerevanian; Ralph J. Koek; Jim Mintz

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Jim Mintz

University of California

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Cole J. Marta

University of California

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Wesley C. Ryan

University of Washington

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