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1.
Nat Rev Dis Primers ; 10(1): 49, 2024 Jul 18.
Article in English | MEDLINE | ID: mdl-39025858

ABSTRACT

Catatonia is a neuropsychiatric disorder characterized by motor, affective and cognitive-behavioural signs, which lasts from hours to days. Intensive research over the past two decades has led to catatonia being recognized as an independent diagnosis in the International Classification of Diseases, 11th Revision (ICD-11) since 2022. Catatonia is found in 5-18% of inpatients on psychiatric units and 3.3% of inpatients on medical units. However, in an unknown number of patients, catatonia remains unrecognized and these patients are at risk of life-threatening complications. Hence, recognizing the symptoms of catatonia early is crucial to initiate appropriate treatment to achieve a favourable outcome. Benzodiazepines such as lorazepam and diazepam, electroconvulsive therapy, and N-methyl-D-aspartate antagonists such as amantadine and memantine, are the cornerstones of catatonia therapy. In addition, dopamine-modulating second-generation antipsychotics (for example, clozapine and aripiprazole) are effective in some patient populations. Early and appropriate treatment combined with new screening assessments has the potential to reduce the high morbidity and mortality associated with catatonia in psychiatric and non-psychiatric settings.


Subject(s)
Benzodiazepines , Catatonia , Electroconvulsive Therapy , Catatonia/diagnosis , Catatonia/therapy , Catatonia/physiopathology , Catatonia/etiology , Humans , Electroconvulsive Therapy/methods , Benzodiazepines/therapeutic use , Lorazepam/therapeutic use , Antipsychotic Agents/therapeutic use , Amantadine/therapeutic use , Memantine/therapeutic use , Diazepam/therapeutic use
3.
Asian J Psychiatr ; 96: 104033, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38564875

ABSTRACT

BACKGROUND: Catatonia is a highly prevalent syndrome in patients presenting with major neurocognitive disorders (dementia). In this study, we aim to provide a comprehensive description of the clinical and therapeutic aspects of catatonia in patients with dementia. METHOD: This descriptive study, conducted between September 2015 and June 2022, collected data from 25 patients diagnosed with dementia, out of 143 patients treated for catatonia in our specialized psychiatry department. We collected sociodemographic, clinical and treatment data for each patient. RESULTS: Dementia patients constituted 17% of the catatonic cases. Predominantly female, the cohort had a mean age of 65. Diagnoses included Alzheimer's (4 patients, 17%) and Parkinson's (1 patient, 4%) diseases, Lewy body dementia (5 patients, 21%), vascular dementia (4 patients, 17%) and frontotemporal lobar degeneration (10 patients, 41%). The mean Bush-Francis Catatonia Rating Scale score upon admission was 20/69. Overall, complete remission of catatonia was achieved in 75% of patients (n=18), with only 13% (n=3) responding to lorazepam alone, while others required additional interventions such as electroconvulsive therapy (ECT) and/or amantadine. Vascular dementia was predominantly observed in cases resistant to treatment. CONCLUSION: The findings indicate a frequent co-occurrence of catatonia and dementia, highlighting treatability yet suggesting a potential for resistance to lorazepam, which varies by dementia diagnosis. Investigating the mechanisms underlying this resistance and the variability in treatment response is crucial for developing more precise therapeutic strategies.


Subject(s)
Catatonia , Dementia , Electroconvulsive Therapy , Humans , Catatonia/therapy , Catatonia/drug therapy , Catatonia/etiology , Female , Male , Aged , Dementia/complications , Electroconvulsive Therapy/methods , Middle Aged , Lorazepam/therapeutic use , Aged, 80 and over , Comorbidity , Treatment Outcome
4.
Medicine (Baltimore) ; 103(14): e37730, 2024 Apr 05.
Article in English | MEDLINE | ID: mdl-38579062

ABSTRACT

RATIONALE: Turner syndrome (TS) is a genetic disorder associated with partial or complete monosomy X abnormalities; some patients may have a higher risk of psychiatric symptoms. Catatonia is associated with a wide range of life-threatening complications with complex pathogenesis; However, It very rare for patients with TS to develop psychotic symptoms and eventually progress to catatonia. This case report describes the diagnostic and therapeutic course of catatonia-associated TS. PATIENT CONCERNS: In this study, we report the case of a patient with TS who initially developed sudden hallucinations, delusions, and emotional instability, followed by catatonia. DIAGNOSES: The patient was diagnosed with: unspecified catatonia; TS. INTERVENTIONS: Treatment included administering a combination of esazolam injections and olanzapine tablets, placing a gastric tube and urinary catheter, and providing nutritional support. OUTCOMES: After treatment, the patient's hallucinations, delusions, and catatonia disappeared, with no residual sequelae, and social functioning returned to normal. LESSONS: For patients with TS who present with psychotic symptoms and catatonia, a comprehensive evaluation is necessary, and treatment with antipsychotics and benzodiazepines is effective.


Subject(s)
Antipsychotic Agents , Catatonia , Psychotic Disorders , Turner Syndrome , Humans , Catatonia/etiology , Catatonia/therapy , Catatonia/diagnosis , Turner Syndrome/complications , Psychotic Disorders/etiology , Psychotic Disorders/drug therapy , Antipsychotic Agents/therapeutic use , Hallucinations/complications
5.
Actas Esp Psiquiatr ; 52(2): 183-188, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38622014

ABSTRACT

BACKGROUD: Catatonia encompasses a group of severe psychomotor syndromes affecting patients' motor, speech, and complex behaviors. Common features include rigidity, reduced mobility, speech, sputum production, defecation, and eating. Risks associated with catatonia, such as increased muscle tension and reduced swallowing and coughing reflexes, along with risks from therapeutic approaches like prolonged bed rest and sedative drugs, can elevate the risk of aspiration pneumonia, severe pneumonia, and acute respiratory failure. These complications significantly impede catatonia treatment, leading to poor prognosis and jeopardizing patient safety. CASE DESCRIPTION: In this report, we present a case of catatonia complicated by severe pneumonia and respiratory failure, successfully managed with modified electroconvulsive therapy alongside tracheotomy. We hope this case provides valuable insights for psychiatrists encountering similar scenarios, facilitating the development of rational therapeutic strategies for prompt improvement of patient condition.


Subject(s)
Catatonia , Electroconvulsive Therapy , Pneumonia , Respiratory Insufficiency , Humans , Tracheotomy/adverse effects , Catatonia/therapy , Catatonia/drug therapy , Pneumonia/complications , Respiratory Insufficiency/complications , Respiratory Insufficiency/therapy
6.
Turk Psikiyatri Derg ; 35(1): 78-82, 2024.
Article in English, Turkish | MEDLINE | ID: mdl-38556940

ABSTRACT

Electroconvulsive therapy (ECT) is an effective and safe treatment method for many psychiatric disorders. In general medical practice, ECT may cause side effects as most other treatment methods do. Headache, myalgia, nausea, vomiting, confusion, anterograde amnesia are common side effects of electroconvulsive therapy. Fever; in addition to general medical conditions such as infection, malignancy, connective tissue diseases, drug treatments, malignant hyperthermia, convulsions, it can also occur due to conditions such as neuroleptic malignant syndrome (NMS), serotonin syndrome, catatonia, malignant catatonia, which are frequently encountered in psychiatry clinics. In the literature, transient fever response due to electroconvulsive therapy application have been described, albeit rarely. Although there are many proposed mechanisms for the emergence of a fever response, regardless of its cause, it is still not understood why some fever responses occur. In this article, we present the differential diagnosis of the fever response, possible causes, and the mechanisms that may reveal the secondary fever response to electroconvulsive therapy in a case with a diagnosis of catatonic schizophrenia, who developed a fever response during electroconvulsive therapy sessions and no fever response was observed at times other than electroconvulsive therapy sessions. In this case, postictal benign fever response associated with electroconvulsive therapy was considered after excluding other medical conditions that may cause a fever response after electroconvulsive therapy. Keywords: ECT, Fever, Catatonia, NMS.


Subject(s)
Catatonia , Electroconvulsive Therapy , Neuroleptic Malignant Syndrome , Schizophrenia , Humans , Schizophrenia, Catatonic/complications , Schizophrenia, Catatonic/therapy , Catatonia/etiology , Catatonia/therapy , Catatonia/diagnosis , Schizophrenia/complications , Schizophrenia/therapy , Electroconvulsive Therapy/adverse effects , Electroconvulsive Therapy/methods , Neuroleptic Malignant Syndrome/complications , Neuroleptic Malignant Syndrome/diagnosis
7.
Curr Opin Crit Care ; 30(2): 151-156, 2024 04 01.
Article in English | MEDLINE | ID: mdl-38441073

ABSTRACT

PURPOSE OF REVIEW: The rising prevalence of neurodegenerative and mental disorders, combined with the challenges posed by their frailty, has presented intensivists with complex issues in the intensive care unit (ICU). This review article explores specific aspects of care for patients with catatonia, Parkinson's disease (PD), and dementia within the context of the ICU, shedding light on recent developments in these fields. RECENT FINDINGS: Catatonia, a neuropsychiatric syndrome with potentially life-threatening forms, remains underdiagnosed, and its etiologies are diverse. PD patients in the ICU present unique challenges related to admission criteria, dopaminergic treatment, and respiratory care. Dementia increases the risk of delirium. Delirium is associated with long-term cognitive impairment and dementia. SUMMARY: While evidence is lacking, further research is needed to guide treatment for ICU patients with these comorbidities.


Subject(s)
Catatonia , Delirium , Dementia , Parkinson Disease , Humans , Catatonia/diagnosis , Catatonia/therapy , Catatonia/complications , Parkinson Disease/complications , Parkinson Disease/therapy , Dementia/therapy , Dementia/complications , Delirium/diagnosis , Delirium/etiology , Delirium/therapy , Intensive Care Units
9.
Tijdschr Psychiatr ; 66(1): 46-50, 2024.
Article in Dutch | MEDLINE | ID: mdl-38380488

ABSTRACT

Catatonia in children and adolescents is not rare and, as in adults, has a favorable outcome, provided it is recognized and treated promptly. Nevertheless, in clinical practice we encounter several obstacles in terms of diagnosis and treatment in this population of patients. We describe a 14-year-old boy with an intellectually disability and autism spectrum disorder (ASD) in which clinicians did not diagnose catatonia until 1 year after the development of symptoms. Moreover, hesitations surrounding the correct treatment led to its delayed initiation. With this case report we aim to contribute to reduced reluctance and increased alertness in the treatment of catatonia in adolescents with developmental disorders.


Subject(s)
Autism Spectrum Disorder , Catatonia , Male , Child , Adult , Humans , Adolescent , Catatonia/diagnosis , Catatonia/therapy , Autism Spectrum Disorder/diagnosis , Autism Spectrum Disorder/therapy , Autism Spectrum Disorder/epidemiology , Developmental Disabilities/diagnosis , Developmental Disabilities/therapy
11.
BMJ Case Rep ; 17(1)2024 Jan 04.
Article in English | MEDLINE | ID: mdl-38176751

ABSTRACT

The authors describe a female in her late twenties, presenting with catatonia and diagnosed with epilepsy, autism spectrum disorder, mild intellectual disability, psychosis, dysthymia, anxiety and bipolar disorder, receiving weekly electroconvulsive therapy (ECT). After testing, findings indicated an interstitial deletion in the 22q13.33 region associated with Phelan-McDermid syndrome. In addition, the patient had low cerebral spinal fluid tetrahydrobiopterin (BH4) levels, suggesting dysfunction in the pterin biosynthetic pathway. As a result, the patient started on sapropterin, a BH4 replacement small molecule. After sapropterin treatment, catatonia improved, and the need for ECT decreased. There was an improvement in her cognitive ability, attention and independence. However, there has been no improvement in seizure frequency.


Subject(s)
Autism Spectrum Disorder , Autistic Disorder , Catatonia , Chromosome Disorders , Depressive Disorder, Major , Phenylketonurias , Female , Humans , Autism Spectrum Disorder/complications , Autistic Disorder/complications , Autistic Disorder/genetics , Catatonia/diagnosis , Catatonia/therapy , Catatonia/complications , Chromosome Deletion , Chromosome Disorders/complications , Chromosomes, Human, Pair 22 , Depression , Depressive Disorder, Major/complications , Phenylketonurias/complications , Adult
12.
Schizophr Res ; 263: 246-251, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37087393

ABSTRACT

Electroconvulsive therapy (ECT) is a safe and effective treatment for catatonia with high response rates. Although empirical data suggest that tolerability and efficacy are at least as good as in adults, ECT treatment of children, adolescents, and geriatric patients seems to pose a specific challenge for many practitioners. This article intends to explore and discuss reasons hindering the use of ECT in these patient groups, give an overview on the use of ECT to treat catatonia and provide practical advice on ECT in children, adolescents, and geriatric patients for the treatment of catatonia. Classification of catatonia as a subform of schizophrenia and a diagnostic overlap with other common conditions in children, adolescents, and geriatric patients might lead to underdiagnosis of catatonia. Concerns about the mechanism of action and about a lack of controlled studies as well as general concerns about the use of ECT in children and adolescents might lead to underutilization of ECT. However, studies of ECT to treat catatonia in children, adolescents, and geriatric patients consistently show its safety and effectiveness. Administration of ECT needs to consider some specific characteristics of children, adolescents, and geriatric patients. In conclusion, ECT is a safe and highly effective treatment for catatonia across the lifespan. Existing evidence does not warrant restrictions of its use in certain age groups.


Subject(s)
Catatonia , Electroconvulsive Therapy , Schizophrenia , Adult , Adolescent , Child , Humans , Aged , Catatonia/therapy , Longevity , Schizophrenia/therapy , Treatment Outcome
13.
J Am Acad Child Adolesc Psychiatry ; 63(3): 293-295, 2024 Mar.
Article in English | MEDLINE | ID: mdl-37778726

ABSTRACT

In a recent letter to the editor, Dr. Miller and colleagues1 highlighted the disparity of electroconvulsive therapy (ECT) across different states, and the challenges faced by a patient in Colorado for whom ECT was deemed the most appropriate treatment but was not available in this location, forcing the patient to seek care in New Mexico. A subsequent letter by Dr. Ong and colleagues2 presented an additional case, in a different location, where a delay in ECT treatment because of state regulations contributed to substantial patient morbidity. In this letter, we present a patient seen at our facility in California, a state with some of the most stringent regulations regarding ECT treatment in adolescents.3 This case illustrates how ECT was eventually approved by the court system only after the patient's continual deterioration, despite receiving intensive medical treatment on an inpatient pediatric medical unit for a duration of 80 days. Care providers and the patient's family were forced to witness this decline until the patient reached "an emergency situation" and ECT was "deemed a lifesaving treatment," as the California Welfare and Institutions Code (WIC) § 5,326.8(a) forbids the procedure under any other circumstances.


Subject(s)
Autism Spectrum Disorder , Catatonia , Electroconvulsive Therapy , Child , Adolescent , Humans , Catatonia/therapy , Autism Spectrum Disorder/therapy
14.
Int Clin Psychopharmacol ; 39(2): 113-116, 2024 Mar 01.
Article in English | MEDLINE | ID: mdl-37729655

ABSTRACT

Paternal postpartum depression (PD) is considered an affective disorder that affects fathers during the months following childbirth. Interestingly, it has been observed that during these months the chances of a male parent suffering from depression are double that for a non-parent male counterpart. We present the case of a 34-year-old man with no relevant medical history in who, overlapping her daughter's birth, several depressive symptoms emerged, such as fatigue, lack of concentration, sleeping disturbances and abandonment of care of the newborn. Prior to consultation, patient refused to eat and open his eyes, and his speech became progressively more parsimonious until reaching mutism. The patient was diagnosed with a severe depressive disorder with catatonia. Given the lack of improvement with pharmacological treatment and due to the evidence of electroconvulsive therapy (ECT)'s effectiveness on patients with catatonia, acute ECT treatment was indicated and started. It should be noted that PD is an important entity to consider in our differential diagnosis of young parents who present a depressive episode. Few cases of relatively young patients presenting with such clinical presentation have been described and, although this case presents some of the characteristics described in the epidemiology of PD, other clinical aspects are not typical of this entity. Informed consent was obtained from the patient for the purpose of publication.


Subject(s)
Bipolar Disorder , Catatonia , Depression, Postpartum , Electroconvulsive Therapy , Female , Infant, Newborn , Humans , Male , Adult , Bipolar Disorder/diagnosis , Bipolar Disorder/therapy , Bipolar Disorder/psychology , Catatonia/therapy , Catatonia/drug therapy , Depression/diagnosis , Depression/therapy , Depression, Postpartum/diagnosis , Depression, Postpartum/therapy , Depression, Postpartum/complications , Fathers , Postpartum Period
15.
Pharmacopsychiatry ; 57(1): 13-20, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37995719

ABSTRACT

INTRODUCTION: Electroconvulsive therapy (ECT) is known to be effective in the treatment of catatonia, reaching response rates of about 80 to 100%. It is indicated in cases of treatment resistance to benzodiazepines and in life-threatening conditions such as malignant catatonia. Beneficial effects on specific symptoms or predictors of response are less clear. The objective of this retrospective study is to examine the ECT effect on specific catatonia symptoms in the acute phase of the illness and to identify predictors of response. METHODS: A retrospective study examined data from 20 patients with catatonia, 18 associated with schizophrenia and 2 with bipolar disorder, who underwent ECT from 2008 to 2021. Ten subjects had more than one ECT-series, resulting in a total of 31 ECT-series. Catatonia symptom severity was assessed with the Bush Francis Catatonia Rating Scale (BFCRS). RESULTS: ECT yielded excellent response. Nineteen of 20 patients and 30 of 31 ECT-series achieved response. The mean number of ECT sessions to response was 4.2. Response to ECT was more pronounced for motor inhibition symptoms such as stupor and mutism, while echophenomena, dyskinesia, stereotypy and perseveration responded less well. A predictor of late response was the presence of grasp reflex. DISCUSSION: The present study corroborates the high and rapid effectiveness of ECT in the treatment of catatonia. Focus on single catatonia signs may help to identify those who are most likely to achieve remission quickly, as well as those who might need longer ECT-series.


Subject(s)
Bipolar Disorder , Catatonia , Electroconvulsive Therapy , Schizophrenia , Humans , Catatonia/therapy , Electroconvulsive Therapy/methods , Retrospective Studies , Schizophrenia/therapy , Bipolar Disorder/complications , Bipolar Disorder/therapy
16.
J Neuroimmunol ; 386: 578271, 2024 01 15.
Article in English | MEDLINE | ID: mdl-38155066

ABSTRACT

BACKGROUND: Anti-NMDAR encephalitis is the most common cause of immune-mediated catatonia. CASE SERIES: Three females presented with neuropsychiatric symptoms and were empirically treated with first-line immunotherapy and ovarian teratoma resection for suspected autoimmune encephalitis, preceding diagnostic confirmation via NMDAR antibody positivity. They required escalating large doses of benzodiazepines for refractory malignant catatonia resulting in ICU level care. ECT treatments were initiated, and patients were gradually noted to have clinical improvement as was measured by the Bush-Francis Catatonia Rating Scale. CONCLUSIONS: Clinicians should recognize catatonia among patients with suspected anti-NMDAR encephalitis and consider the early implementation of ECT into treatment algorithms.


Subject(s)
Anti-N-Methyl-D-Aspartate Receptor Encephalitis , Catatonia , Electroconvulsive Therapy , Ovarian Neoplasms , Female , Humans , Catatonia/etiology , Catatonia/therapy , Anti-N-Methyl-D-Aspartate Receptor Encephalitis/complications , Anti-N-Methyl-D-Aspartate Receptor Encephalitis/diagnostic imaging , Anti-N-Methyl-D-Aspartate Receptor Encephalitis/therapy , Electroconvulsive Therapy/methods , Ovarian Neoplasms/complications , Ovarian Neoplasms/therapy , Receptors, N-Methyl-D-Aspartate
18.
N Engl J Med ; 389(19): 1797-1802, 2023 Nov 09.
Article in English | MEDLINE | ID: mdl-37937779
20.
Psychiatry Res ; 330: 115580, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37926055

ABSTRACT

Electroconvulsive Therapy (ECT) is an effective treatment for mood and psychotic disorders but there is growing evidence of treatment resistant to ECT. Our study aimed to investigate the relationship between the number of previous illness episodes and the symptomatic improvement after acute ECT treatment. We conducted a retrospective naturalistic cohort analysis of patients' ECT registry data from March 2017 to February 2023. We categorized the number of previous illness episodes into "0-3″ and ">3 episodes", paired T-tests were used to compare the changes in scores of clinical assessments, generalized linear models were used to analyze the association between the number of previous illness episodes and change in symptomatic scores. A total of 1137 patients were included for analysis. There was a significant global improvement in psychiatric symptoms (CGI) after 6 ECT treatments across five indications. We observed that compared to patients with less previous illness episodes, patients with more than 3 previous illness episodes had 30% lower chance of response to acute ECT treatment. Thus, our study suggests that use ECT earlier in the course of illness is associated with greater response and support offering ECT earlier in the disease course.


Subject(s)
Catatonia , Electroconvulsive Therapy , Psychotic Disorders , Humans , Mania , Depression , Retrospective Studies , Catatonia/therapy , Psychotic Disorders/therapy , Treatment Outcome
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