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1.
Psychiatry Res ; 337: 115967, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38796933

ABSTRACT

The role of the endocannabinoid system (ECS) in depression and suicidality has recently emerged. The purpose of the study was to identify changes in plasma endocannabinoid concentrations of several endocannabinoids and correlate them with depressive symptoms and suicidality in patients with severe major depression undergoing electroconvulsive therapy (ECT). The study included 17 patients that were evaluated in four visits at different stages of therapy. At each visit depression, anxiety and suicidality symptoms were assessed and blood samples collected. Several endocannabinoid concentrations increased following six sessions of ECT, as 2-AG (p < 0.05) and LEA (p < 0.01), and following twelve sessions of ECT, as 2-AG (p < 0.05), AEA (p < 0.05), LEA (p < 0.05) and DH-Gly (p < 0.05). Endocannabinoids also correlated with symptoms of depression, anxiety and suicidality at baseline and at the sixth ECT session. Finally, we found one endocannabinoid, l-Gly, that differentiated between remitted and not-remitted patients at the seventh and thirteenth ECT sessions (p < 0.05). Our findings suggest that depression is markedly related to imbalance of the endocannabinoid system, and further regulated by ECT. Plasma endocannabinoids could be promising biomarkers for detection of depression response and remission.


Subject(s)
Depressive Disorder, Major , Electroconvulsive Therapy , Endocannabinoids , Humans , Endocannabinoids/blood , Depressive Disorder, Major/blood , Depressive Disorder, Major/therapy , Female , Male , Middle Aged , Adult , Arachidonic Acids/blood , Aged , Polyunsaturated Alkamides/blood , Glycerides/blood , Oleic Acids/blood , Psychiatric Status Rating Scales , Suicidal Ideation
2.
J Psychiatr Res ; 174: 66-72, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38626563

ABSTRACT

One in five people will likely suffer from major depressive disorder (MDD) during their life. Thirty percent of those with MDD will experience Treatment Resistant Depression (TRD), which is characterized by a failure to respond to two adequately administered trials of antidepressants. Esketamine is a rapidly acting intranasal antidepressant. Present-day Esketamine research has limited data in real-world populations. This study aimed to assess Esketamine treatment in a real-world community-based population. This naturalistic retrospective study included 94 individuals age 18 and above diagnosed with TRD, treated with Esketamine in an outpatient setting. The treatment was given in a single clinic, from January 2021 to January 2023, following approval of the Institutional Internal Review Board. The treatment included an acute phase (biweekly treatment, continuing 4-8 weeks), followed by a maintenance phase (once a week to once a month, for 6-12 months). Dosing ranged from 28 mg to 84 mg. Demographic and clinical data were retrospectively gathered. Depressive symptoms were assessed using the Quick Inventory of Depressive Symptomatology, at baseline and during each treatment phase. All patients completed the acute phase. About 60% completed the maintenance phase. Linear improvement of depressive symptoms was revealed in both phases. A sub-analysis of patients with comorbid personality disorder revealed a similar improvement pattern in the acute phase with milder improvement during the maintenance phase, compared to the other patients. This study supports the use of Esketamine for TRD, including patients with comorbid personality disorder and previous electroconvulsive therapy.


Subject(s)
Antidepressive Agents , Depressive Disorder, Treatment-Resistant , Ketamine , Humans , Ketamine/administration & dosage , Ketamine/pharmacology , Depressive Disorder, Treatment-Resistant/drug therapy , Male , Female , Middle Aged , Adult , Retrospective Studies , Israel , Antidepressive Agents/administration & dosage , Administration, Intranasal , Depressive Disorder, Major/drug therapy , Aged , Young Adult , Outcome Assessment, Health Care
3.
Front Psychiatry ; 15: 1293676, 2024.
Article in English | MEDLINE | ID: mdl-38487572

ABSTRACT

Introduction: Chloral hydrate (CH), a medication dating back to 1832, is tranquilizer and sleep promoter still used today. It remains an option for short-term insomnia therapy and sedation before medical procedures, despite its controversial safety profile. Methods: This study investigated the potential benefits of chloral hydrate addition for increasing sleep duration and reducing agitation and violence in inpatients with treatment-resistant schizophrenia (TRS). A retrospective, observational case series design was utilized, analyzing data from fourteen patients diagnosed with TRS disorders. Results: CH addition increased the rate of full night sleep and decreased the rates of agitation and verbal and physical violence events. Notably, no adverse events including falls were reported during CH addition. Discussion: CH shows some short-term benefits in improving sleep disorders and reducing violent and agitated behavior in patients with TRS. Our study has limitations due to its small sample size, retrospective design and lack of a control group. A large-scale, double-blind, randomized trial is needed to further explore the efficacy and safety of CH in psychiatric populations with TRS accompanied by agitation, violence and disturbed sleep.

4.
Harefuah ; 162(8): 518-523, 2023 Sep.
Article in Hebrew | MEDLINE | ID: mdl-37698332

ABSTRACT

INTRODUCTION: A history of sexual trauma (ST) and, especially, of childhood sexual abuse (CSA) is common among men and women with mental disorders. The estimated prevalence ranges between one-third to two-thirds of psychiatric patients who have experienced sexual trauma. These survivors are at increased risk for developing psychiatric disorders, including schizophrenia and bipolar disorder. Despite the great prevalence of sexual trauma and its mental implications, it remains under-diagnosed and under-recognized within the mental health system in Israel, as well as worldwide. This is due to the absence of a suitably comprehensive procedure for taking patient histories that will uncover sexual trauma. A history of sexual trauma also has implications for the course of the illness and prognosis. Trauma-informed treatment for survivors can reduce symptoms and alleviate mental suffering even many years after the traumatic events.


Subject(s)
Bipolar Disorder , Male , Humans , Female , Israel/epidemiology , Mental Health , Sexual Trauma , Hospitalization
5.
Clin Neuropharmacol ; 2023 Jun 20.
Article in English | MEDLINE | ID: mdl-37335845

ABSTRACT

OBJECTIVES: The mechanism of inflammation of the immune system, for example, such circulatory markers as the neutrophil-to-lymphocyte ratio (NLR) and mean platelet volume (MPV), has been shown in many studies to be associated with schizophrenia. In addition, it has been shown that the cannabidiol component reduces the activation of the acquired immune system. This study examined the differences in the levels of NLR and MPV among schizophrenia patients with cannabis use versus those without. METHODS: In 2019 to 2020, a retrospective cross-sectional study was conducted based on digital medical records. Demographic, clinical, and complete blood cell count data were collected from records of rehospitalization of active psychotic schizophrenia inpatients. Data on NLR, MPV values, and demographic and clinical characteristics were compared between the groups and according to the degree of prevalence of cannabis use. RESULTS: No differences were found in the NLR and MPV values between the groups. CONCLUSION: The results were contrary to our expectations. These results may be explained by the presentation of a "pseudo-balanced" picture created when multiple processes affect inflammatory indices.

6.
J Eval Clin Pract ; 28(6): 948-957, 2022 12.
Article in English | MEDLINE | ID: mdl-35731528

ABSTRACT

RATIONALE AND OBJECTIVE: At the beginning of vaccination against coronavirus disease 2019 (COVID-19), information about the effects of the vaccine was not known and hesitancy was observed among the population. The mental health staff members in our center in Israel had to decide whether to get vaccinated or not. The objective of this study was to evaluate the differences in demographic characteristics of vaccinated and nonvaccinated mental health care workers (HCWs), and to identify their reasons for or against vaccination. METHOD: Data on characteristics of 357 staff members at a mental health center (MHCS) in Israel and their attitudes regarding COVID-19 vaccination, those who were nonvaccinated, were collected via anonymous questionnaires, from 1 January to 10 January 2021. The groups were then compared using χ2 , Fisher's exact tests, t test or Mann-Whitney nonparametric test as appropriate. A logistic regression was then performed using the significant variables and odd ratios presented. RESULTS: Eighty-one per cent of the sample received at least the first dose of the vaccine. Results indicated differences in seniority (p < 0.001), profession (p < 0.001), department (p < 0.001), risk groups (p < 0.05), religion (p < 0.001), religiosity (p < 0.001), previous care for COVID-19 patients (p < 0.05) and level of interaction with patients (p < 0.01), between the vaccinated and nonvaccinated staff. The factor that was found to be most influential regarding vaccination and which convinced those originally against the vaccine to become vaccinated was the level of scientific knowledge about the vaccine. CONCLUSION: Efforts and resources should focus on the dissemination of reliable scientific data about the vaccine, to increase vaccination rates among mental HCWs.


Subject(s)
COVID-19 , Influenza Vaccines , Influenza, Human , Humans , COVID-19/epidemiology , COVID-19/prevention & control , COVID-19 Vaccines , Influenza, Human/prevention & control , Mental Health , Cross-Sectional Studies , Vaccination
7.
Isr Med Assoc J ; 24(2): 74-77, 2022 Feb.
Article in English | MEDLINE | ID: mdl-35187893

ABSTRACT

BACKGROUND: Risk factors for severe coronavirus disease-2019 (COVID-19) infection include old age, chronic illness, and neurological conditions. In contrast, high vitamin D levels are known to augment immune activity and to reduce the severity of viral infections. Recently, a possible association between the likelihood of COVID-19 infection, COVID-19 severity, and vitamin D blood levels was reported. OBJECTIVES: To assess the possible association between vitamin D long-term supplementation and COVID-19 symptomatic severity and complications of COVID-19 infection in elderly psychiatric inpatients, a high at-risk group. METHODS: We conducted a retrospective case series study. Data of 14 elderly COVID-19 positive inpatients, presenting with dementia or schizophrenia and other medical conditions were extracted from medical records. All patients maintained a 800 IU daily dose of vitamin D prior to the infection. RESULTS: Most of the inpatients were asymptomatic or presented very few symptoms. No need for intensive care unit intervention or deaths were reported. Cognitive functioning of the patients remained unchanged. CONCLUSIONS: Pre-existing vitamin D supplementation may reinforce immunity and reduce COVID-19 severity in elderly psychiatric inpatients.


Subject(s)
COVID-19/physiopathology , Dementia/epidemiology , Schizophrenia/epidemiology , Vitamin D/administration & dosage , Aged , Aged, 80 and over , COVID-19/complications , COVID-19/immunology , Dietary Supplements , Female , Humans , Inpatients , Male , Patient Acuity , Protective Factors , Retrospective Studies , Risk Factors , Vitamin D/blood
8.
Int Clin Psychopharmacol ; 37(1): 9-13, 2022 01 01.
Article in English | MEDLINE | ID: mdl-34825897

ABSTRACT

Many psychotic patients are treated with antipsychotic medications during acute agitation and aggressive behavior episodes in an attempt to achieve a rapid calming effect. Those medications include olanzapine, zuclopenthixol acetate, and haloperidol intramuscular administration. This study compared the effectiveness of these injections in reducing the need for restraint during agitated-psychotic episodes that include aggression. Sociodemographical and clinical data were retrieved from the electronic medical records of 179 patients who needed rapid calming while hospitalized in a mental health center with acute psychosis. The treatments administered were olanzapine intramuscular, zuclopenthixol acetate intramuscular, and haloperidol intramuscular. The assessed outcomes were rate of restraint and violent behavior. Olanzapine was found significantly more effective in reducing the need for restraint compared to zuclopenthixol acetate. No significant differences were found between haloperidol and the other two with regard to restraint. Neither were other significant differences found between the groups with regard to violent or self-harming behaviors. No significant differences were found in the rate of violent behavior and antipsychotic dosage at discharge. In conclusion, in inpatients with acute agitated psychosis, olanzapine intramuscular shows better efficacy in reducing the need for restraint, at least as compared to zuclopenthixol acetate intramuscular.


Subject(s)
Antipsychotic Agents , Psychotic Disorders , Antipsychotic Agents/adverse effects , Benzodiazepines/adverse effects , Clopenthixol/analogs & derivatives , Clopenthixol/therapeutic use , Haloperidol/adverse effects , Haloperidol/therapeutic use , Humans , Injections, Intramuscular , Olanzapine/therapeutic use , Psychomotor Agitation/drug therapy , Psychotic Disorders/drug therapy , Psychotic Disorders/psychology
9.
J Clin Psychopharmacol ; 41(6): 629-631, 2021.
Article in English | MEDLINE | ID: mdl-34735098

ABSTRACT

BACKGROUND: Weight gain due to antipsychotics is a challenging clinical problem because, to date, no effective pharmacological strategies have been found. Bupropion is often used in people with schizophrenia for smoking cessation and is well tolerated. However, studies on its use as weight loss treatment are scarce. The aim of the study was to examine the effectiveness of bupropion as a single weight loss treatment in overweight individuals maintained on long-term olanzapine or risperidone. METHODS: This randomized, double-blind, placebo-controlled, 8-week study included 26 overweight (body mass index ≥27 kg/m2) individuals with schizophrenia maintained on olanzapine (10-20 mg/d) or risperidone (2-4 mg/d). Participants were randomly allocated to a study group that received bupropion (150-300 mg/d) or to a placebo group. The positive and Negative Syndrome Scale and the Clinical Global Impression-Severity Scale were used to assess severity of psychosis at baseline and end of study (8 weeks). RESULTS: Bupropion addition, but not placebo, was associated with a significant reduction in body weight. Severity of psychotic symptoms was not altered in either group. CONCLUSIONS: The results demonstrate the efficacy of bupropion, compared with placebo, in patients maintained on chronic treatment with olanzapine or risperidone, both known to be major contributors to significant weight gain.


Subject(s)
Antipsychotic Agents/pharmacology , Bupropion/pharmacology , Dopamine Uptake Inhibitors/pharmacology , Olanzapine/pharmacology , Overweight/drug therapy , Risperidone/pharmacology , Schizophrenia/drug therapy , Adult , Antipsychotic Agents/administration & dosage , Bupropion/administration & dosage , Dopamine Uptake Inhibitors/administration & dosage , Double-Blind Method , Female , Humans , Male , Middle Aged , Olanzapine/administration & dosage , Outcome Assessment, Health Care , Risperidone/administration & dosage , Secondary Prevention
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