Catatonia Clinical Presentation
- Author: James Robert Brasic, MD, MPH; Chief Editor: Selim R Benbadis, MD more...
History
Catatonia is a syndrome—typically episodic, with periods of remission—characterized by the presence of a variety of behavioral and motoric traits. The accurate, prompt diagnosis of catatonia is crucial to prevent morbidity and death in a variety of settings, including emergency medical, psychiatric, neurologic, medical, obstetric, and surgical ones, and to institute effective interventions.
While individuals with catatonia often cannot provide a coherent history, collateral sources can often relate relevant historical information. Family members can confirm the presence of typical primary features of catatonia, including immobility, stupor, posturing, rigidity, staring, grimacing, and withdrawal.
A history of behavioral responses to others usually includes the presence of the following:
- Mutism
- Negativism
- Echopraxia
- Echolalia
- Waxy flexibility
- Withdrawal
A history of stereotypies, mannerisms, and verbigeration is often elicited from people who are close to the patient. Priapism was reported in a 20-year-old man with paranoid schizophrenia and catatonia.[47]
The alternative presentation of catatonia is an excited state, possibly with impulsivity, combativeness, and autonomic instability. While a history of an excited state should be sought from the family of a person with catatonia, it is often denied by the family. When present, excited episodes are short-lived and may precipitate collapse with exhaustion. An excited state of catatonia is usually associated with bipolar disorder.
During the initial interview of the patient and the family, elicit a history of possible precipitating events, including infection, trauma, and exposure to toxins and other substances.
A history of similar episodes of catatonia is important to elicit. Determine whether the precipitating events of the earlier episode are present in the current episode. Record any interventions that relieved catatonia previously.
Catatonia and the related condition, neuroleptic malignant syndrome,[15] may follow the administration of neuroleptic medications. Question the patient and family to elicit a history of exposure to neuroleptics and the other substances associated with catatonia.
Clinicians must identify comorbid disorders, including schizophrenia, mood disorders, psychological stressors, medical conditions, and obstetric conditions.
Catatonia has occurred in patients after treatment with levetiracetam[48] and levofloxacin.[49] Catatonia developed in a 55-year-old woman with schizophrenia who was treated with rimonabant, a cannabinoid receptor (CB1) antagonist.[50]
History in emergency care
In an emergency setting, treatable common causes of catatonia must be rapidly considered and ruled out. The emergency physician must quickly consider the presence of neuroleptic malignant syndrome,[15] encephalitis, nonconvulsive status epilepticus, and acute psychosis. Catatonia has occurred in intensive care units.[51] Since the patients all had serious disorders leading to placement in the intensive care units, the underlying disorders possibly contributed to the development of catatonia in the intensive care units.
A history of exposure to traditional and atypical neuroleptics must be sought. While malignant neuroleptic syndrome often follows the initiation of neuroleptic therapy or an increase in neuroleptic dose, the exposure to neuroleptics may be minimal in some susceptible individuals. For example, Nielsen and Nielsen report the occurrence of the neuroleptic malignant syndrome after a single dose of neuroleptic medication.[28]
In addition, the patient’s history must be evaluated for the following conditions:
- Encephalitis - Determine whether the patient has had sudden onset of headache, fever, and deterioration in mental functioning
- Nonconvulsive status epilepticus - Determine whether the patient has a history of seizures and whether the patient has been prescribed antiepileptic drugs; determine whether electroencephalograms (EEGs) have been performed, and, if so, review the findings
- Acute psychosis - Determine whether the patient has exhibited evidence of delusions and hallucinations and whether he or she has exhibited suicidal or homicidal threats or actions; record any history of prior psychiatric hospitalization and treatment
Physical Examination
Catatonia occurs in children, adolescents, and adults; is associated with a heterogeneous group of comorbid conditions; and is characterized by a variety of symptoms and signs of impairment of the expression of voluntary thoughts and movements.
Assessment of a person with possible catatonia should include unstructured, indirect observation of the person, as well as a direct interview. Patients with catatonia exhibit the same general behaviors whether or not the examiner is present. As discussed below, if a patient demonstrates behaviors consistent with catatonia only in the presence of the examiner, then catatonia is unlikely.
Diagnostic criteria
Diagnostic criteria for catatonia include "motoric immobility, excessive motor activity, extreme negativism or mutism, peculiarities of voluntary movement, and echolalia or echopraxia."[52] Two of the items are required to diagnose catatonia in schizophrenia and mood disorder. Only 1 item is required to diagnose catatonia in general medical conditions.
Peralta and Cuesta hypothesized that a sufficient condition to diagnose catatonia is the presence of 3 of the classic motor signs of catatonia as follows: immobility/stupor, mutism, negativism, oppositionism, posturing, catalepsy, automatic obedience, echophenomena, rigidity, verbigeration, and withdrawal.[53]
Because patients with catatonia may be unable to cooperate with the requests of the examiner, specific neurologic signs characteristic of catatonia must be quickly elicited, especially in emergency settings. In particular, rigidity, gegenhalten, and a grasp reflex are readily apparent signs of catatonia in an emergency setting. During the physical examination, also test for the presence of a grasp reflex, a secondary feature of catatonia.
Excited and immobile states
The predominant activity level of the individual is either markedly slow or extremely high, and the behavior of the patient may shift suddenly and unpredictably from one state to the other.
In the excited state, people with catatonia may injure themselves and assault others. They may also experience autonomic instability manifested by hyperthermia, tachycardia, and hypertension. Individuals in the excited state are at risk of collapse from exhaustion.
In the immobile state, the individual may not move. Akinesia and stupor are synonyms for this state. The patient may appear unresponsive to external stimuli. He or she may be unable to eat and therefore may die unless parenteral nutrition and fluids are administered. People with catatonia may exhibit catalepsy, the persistent maintenance of spontaneous or imposed postures.
Negativistic phenomena
Negativistic phenomena are observed typically in catatonia. These include gegenhalten and mitgehen.
Examination should include checking for cogwheeling at the wrist and elbow. Instruct patients to keep their arms loose and limp (like a dead fish) and move the arms of the patients with varying degrees of force. Rigidity is commonly elicited in the extremities of patients with catatonia. The particular phenomenon of gegenhalten is characteristic in catatonia. Patients with gegenhalten demonstrate increasing resistance to passive movement of the limbs. The patient appears to be deliberately opposing the movements of the examiner.
Mitgehen is characterized by the patient moving in the direction of a slight push from the examiner in spite of the command to remain still. The physical examination should include tests for these.
Motor persistence, the maintenance of a posture when commanded to not maintain the posture, is a manifestation of catatonia that is associated with right hemispheric strokes. Other negativistic phenomena are withdrawal from all usual activities and refusal to eat.
Automatic obedience
In addition to negativistic phenomena, individuals with catatonia may display other behaviors indicating inability to appropriately modulate the inhibition of impulses. For example, patients with catatonia may demonstrate automatic obedience, the performance of tasks at the command of the examiner even though the tasks are inappropriate or dangerous.
Stereotypies
Peculiarities of movement are common in catatonia. Stereotypies, in which the patient repetitively performs apparently meaningless activities, are common. These may take the form of repetitive actions or sounds. Verbigeration, or verbal stereotypes, refers to the presence of repetitive, apparently meaningless utterances, such as sniffing, clicking, snorting, and nonmeaningful sounds.
Common motor stereotypies include the following:
- Nose wrinkling
- Repetitive movements of the mouth and the jaw
- Repetitive eye movements
- Repetitive tapping of the foot, the finger, or the hand
- Repetitive abdomen patting, shoulder shrugging, or body rocking
Other movements associated with catatonia include mannerisms, postures, gaze fixation, and choreoathetoid movements of the trunk and extremities.
Preservation
Patients with catatonia may also display preservation, the inappropriate repetition of acts.
Echophenomena
Echophenomena are typical in catatonia. Echolalia, the repetition of the words spoken by the examiner, and echopraxia, the repetition of the motor acts performed by the examiner, are common.
Other considerations
In France, the inappropriately formal use of vous (the formal form of "you") by the patient to address his or her spouse has been identified as a finding in catatonia. (Normally, tu [the informal form of "you"] is used by an individual to address a spouse.)
Clinicians must identify comorbid disorders, including schizophrenia, mood disorders, and neurologic and medical conditions. Neuroleptic-induced parkinsonism may also be associated with catatonia. Headache, fever, and a stiff neck in an acutely ill patient suggest the presence of encephalitis.
The presence of severe muscle rigidity, autonomic dysregulation, and hyperthermia suggests the possibility of a neuroleptic malignant syndrome.
Acute psychosis is suggested by the presence of hallucinations, delusions, and suicidal and homicidal threats and behaviors.
Psychogenic movement disorders
Patients with catatonia exhibit the same general behaviors whether or not the examiner is present. If a patient demonstrates behaviors consistent with catatonia only in the presence of the examiner, then catatonia is unlikely, and conditions characterized by the presence of medical symptoms and signs without physical illness must be considered.
More specifically, catatonia that occurs only when the patient is directly observed by the examiner suggests the presence of somatoform disorders, factitious disorders, or malingering. In the movement disorders literature, somatoform disorders, factitious disorders, and malingering in patients exhibiting abnormal movements are commonly classified as psychogenic movement disorders.
Patients with somatoform disorders, such as somatization disorder, conversion disorder, and hypochondriasis, report symptoms and signs that they truly believe, despite the absence of confirmation on physical examination. Patients with factitious disorders and malingering deliberately report symptoms and signs that they know to be false.
Patients with Munchausen syndrome and other factitious disorders fabricate symptoms and signs because they want to be patients. In Munchausen syndrome by proxy, the parents of the patient, typically an infant unable to communicate, fabricate symptoms and signs in the patient. Unlike patients with factitious disorders, patients with malingering deliberately report false symptoms and signs for specific gain; eg, to obtain disability benefits and to be excused from work.
Ungvari GS, Caroff SN, Gerevich J. The Catatonia Conundrum: Evidence of Psychomotor Phenomena as a Symptom Dimension in Psychotic Disorders. Schizophr Bull. Sep 23 2009;[Medline].
Ungvari GS, Goggins W, Leung SK, Lee E, Gerevich J. Schizophrenia with prominent catatonic features ('catatonic schizophrenia') III. Latent class analysis of the catatonic syndrome. Prog Neuropsychopharmacol Biol Psychiatry. Feb 1 2009;33(1):81-5. [Medline].
Haouzir S, Lemoine X, Desbordes M, Follet M, Meunier C, Baarir Z, et al. The role of coagulation marker fibrin D-dimer in early diagnosis of catatonia. Psychiatry Res. Jun 30 2009;168(1):78-85. [Medline].
Lafargue T, Brasic J. Neurodevelopmental hypothesis of schizophrenia: a central sensory disturbance. Med Hypotheses. Oct 2000;55(4):314-8. [Medline].
Zervas IM, Theleritis C, Soldatos CR. Using ECT in schizophrenia: A review from a clinical perspective. World J Biol Psychiatry. Apr 12 2011;[Medline].
Kannabiran M, McCarthy J. The mental health needs of people with autism spectrum disorders. Psychiatry. Oct 2009;8(10):398-401.
Brasic JR, Zagzag D, Kowalik S, et al. Clinical manifestations of progressive catatonia. German Journal of Psychiatry [serial online]. 2000;[Full Text].
Brasic JR, Zagzag D, Kowalik S, et al. Progressive catatonia. Psychol Rep. Feb 1999;84(1):239-46. [Medline].
Gaind GS, Rosebush PI, Mazurek MF. Lorazepam treatment of acute and chronic catatonia in two mentally retarded brothers. J Clin Psychiatry. Jan 1994;55(1):20-3. [Medline].
Hare DJ, Malone C. Catatonia and autistic spectrum disorders. Autism. Jun 2004;8(2):183-95. [Medline].
Baguley IJ. The excitatory:inhibitory ratio model (EIR model): An integrative explanation of acute autonomic overactivity syndromes. Med Hypotheses. 2008;70(1):26-35. [Medline].
Coconcea C. Zolpidem in treatment resistant catatonia: 2 case reports and literature review [abstract]. Schizophrenia Res. 2008;98:134.
Uzbay IT. L-NAME precipitates catatonia during ethanol withdrawal in rats. Behav Brain Res. Feb 15 2001;119(1):71-6. [Medline].
Kahlbaum KL. Catatonia. Baltimore, Md: Johns Hopkins University Press; 1874/1973.
Vesperini S, Papettia F, Pringuey D. Existe-t-il un lien entre catatonie et syndrome malin des neuroleptiques ? [Are catatonia and neuroleptic malignant syndrome related conditions?]. L'Encéphale. 2009.
Lee J, Teoh T, Lee TS. Catatonia and psychosis associated with sibutramine: a case report and pathophysiologic correlation. J Psychosom Res. Jan 2008;64(1):107-9. [Medline].
Neto B. Catatonia with left temporal lesion on MRI: crossing borders. European Psychiatry. 2009;24 supplement 1:S727.
Wachtel L. Catatonia in autism: Etiology, incidence and treatment [abstract]. European Psychiatry. 2008;23:S402-S402.
Wachtel LE, Contrucci-Kuhn SA, Griffin M, Thompson A, Dhossche DM, Reti IM. ECT for self-injury in an autistic boy. Eur Child Adolesc Psychiatry. Jul 2009;18(7):458-63. [Medline].
Wachtel LE, Griffin M, Reti IM. Electroconvulsive Therapy in a Man With Autism Experiencing Severe Depression, Catatonia, and Self-Injury. J ECT. May 27 2009;[Medline].
Dhossche DM, Reti IM, Wachtel LE. Catatonia and autism: a historical review, with implications for electroconvulsive therapy. J ECT. Mar 2009;25(1):19-22. [Medline].
Wachtel LE. Catatonia in autism and other neurodevelopmental disorders. European Psychiatry. 2009;24, Supplement 1:S737.
Kakooza-Mwesige A, Wachtel LE, Dhossche DM. Catatonia in autism: implications across the life span. Eur Child Adolesc Psychiatry. Sep 2008;17(6):327-35. [Medline].
Gonzalez Oliveros R, Saracibar N, Gutierrez M, DNA Bank UPV/EHU, Munon T, Gonzalez-Pinto A. Catatonia due to a prion familial disease. Schizophrenia Research. Mar 2009;108, Issues 1-3:309-10.
Scozzafava J, Aladdin Y, Jickling G, Asdaghi N, Hussain M, Giuliani F. Stuporous catatonia and white matter lesions. J Clin Neurosci. Oct 2009;16(10):1328, 1386. [Medline].
Blanc F, Berna F, Fleury M, Lita L, Ruppert E, Ferriby D, et al. [Inaugural psychotic events in multiple sclerosis?]. Rev Neurol (Paris). Sep 5 2009;[Medline].
Le Foll J, Pelletier A. Symptômes psychiatriques d'une encéphalite paranéoplasique à anticorps antirécepteurs NMDA : à propos d'un cas [Psychiatric symptoms of a paraneoplastic anti-N-methyl-D-aspartate receptor encephalitis: A case report]. L'Encéphale. 2009.
Nielsen N, Nielsen NB. [Malignant neuroleptic syndrome in a 15-year old girl after a single injection of a high-dose neuroleptic]. Ugeskr Laeger. Aug 5 1991;153(32):2239-40. [Medline].
Winzeler RL. Latah in Southeast Asia: the history and ethnography of a culture-bound syndrome. Cambridge, Great Britain: Cambridge University Press; 1995.
Simons RC. Latah: a culture-specific elaboration of the startle reflex [film]. Bloomington, Indiana: Indiana University Audiovisual Center; 1983.
Tanner CM, Chamberland J. Latah in Jakarta, Indonesia. Mov Disord. May 2001;16(3):526-9. [Medline].
Fink M, Bush G, Francis A. Catatonia: a treatable disorder, occasionally recognized. Directions in Psychiatry. 1993;13(3):1-8.
Escobar R, Rios A, Montoya ID, et al. Clinical and cerebral blood flow changes in catatonic patients treated with ECT. J Psychosom Res. Dec 2000;49(6):423-9. [Medline].
Chalasani P, Healy D, Morriss R. Presentation and frequency of catatonia in new admissions to two acute psychiatricadmission units in India and Wales. Psychol Med. Nov 2005;35(11):1667-75. [Medline].
Peralta V, Cuesta MJ, Serrano JF, Mata I. The Kahlbaum syndrome: a study of its clinical validity, nosological status, and relationship with schizophrenia and mood disorder. Compr Psychiatry. Jan-Feb 1997;38(1):61-7. [Medline].
Vorspan F, Cornic F, Mathis D, Cohen D, Lepine JP. Catatonia in a French forensic psychiatric facility: Frequency, prognosis and treatment [abstract]. European Psychiatry. 2008;23:S332-S333.
Benegal V, Hingorani S, Khanna S. Idiopathic catatonia: validity of the concept. Psychopathology. 1993;26(1):41-6. [Medline].
Johnson J. Catatonia: the tension insanity. Br J Psychiatry. Jun 1993;162:733-8. [Medline].
Rogers D. Catatonia: a contemporary approach. J Neuropsychiatry Clin Neurosci. Summer 1991;3(3):334-40. [Medline].
Ungvari GS, Leung SK, Ng FS, et al. Schizophrenia with prominent catatonic features ('catatonic schizophrenia'): I. Demographic and clinical correlates in the chronic phase. Prog Neuropsychopharmacol Biol Psychiatry. Jan 2005;29(1):27-38. [Medline].
Guggenheim FG, Babigian HM. Catatonic schizophrenia: epidemiology and clinical course. A 7-year register study of 798 cases. J Nerv Ment Dis. Apr 1974;158(4):291-305. [Medline].
Abrams R, Taylor MA. Catatonia. A prospective clinical study. Arch Gen Psychiatry. May 1976;33(5):579-81. [Medline].
Cornic F, Consoli A, Tanguy ML, Bonnot O, Périsse D, Tordjman S, et al. Association of adolescent catatonia with increased mortality and morbidity: evidence from a prospective follow-up study. Schizophr Res. Sep 2009;113(2-3):233-40. [Medline].
Carroll BT. Kahlbaum's catatonia revisited. Psychiatry Clin Neurosci. Oct 2001;55(5):431-6. [Medline].
Bonnot O, Tanguy ML, Consoli A, Cornic F, Graindorge C, Laurent C, et al. Does catatonia influence the phenomenology of childhood onset schizophrenia beyond motor symptoms?. Psychiatry Res. Apr 15 2008;158(3):356-62. [Medline].
Krishna KR, Maniar RC, Harbishettar VS. A comparative study of "idiopathic catatonia'' with catatonia in schizophrenia. Asian J Psych. 2011;4:129-33.
Fischel T, Krivoy A, Brenner I, Weizman A. Priapism as an unusual manifestation of catatonia: a case report. Prog Neuropsychopharmacol Biol Psychiatry. Apr 30 2009;33(3):570. [Medline].
Chouinard MJ, Nguyen DK, Clement JF, Bruneau MA. Catatonia induced by levetiracetam. Epilepsy Behav. Feb 2006;8(1):303-7. [Medline].
Youssef NA, Benazzi F, Desan PH. Levofloxacin-induced catatonia. Prog Neuropsychopharmacol Biol Psychiatry. Jun 15 2009;33(4):741-2. [Medline].
Reddy NN, Rao NP, Venkatasubramanian G, Arasappa R, Behere RV, Divakaran A, et al. Rimonabant-induced catatonia in schizophrenia: A case report. Obesity Research & Clinical Practice. Nov 2009;3 (4):237-239.
Rizos DV, Peritogiannis V, Gkogkos C. Catatonia in the intensive care unit. Gen Hosp Psychiatry. Jan-Feb 2011;33(1):e1-2. [Medline].
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 4th ed. Washington, DC: American Psychiatric Association; 1994.
Peralta V, Cuesta MJ. Motor features in psychotic disorders. II. Development of diagnostic criteria for catatonia. Schizophr Res. Mar 1 2001;47(2-3):117-26. [Medline].
Brasic JR, Barnett JY, Will MV, Nadrich RH, Sheitman BB, Ahmad R, et al. Dyskinesias differentiate autistic disorder from catatonia. CNS Spectr. Dec 2000;5(12):19-22. [Medline].
Denysenko L, Nicolson SE. Cefoxitin and ciprofloxacin neurotoxicity and catatonia in a patient on hemodialysis. Psychosomatics. Jul-Aug 2011;52(4):379-83. [Medline].
Anbarasan D, Campion P, Howard J. Drug-induced leukoencephalopathy presenting as catatonia. Gen Hosp Psychiatry. Jan-Feb 2011;33(1):85.e1-3. [Medline].
Brasic JR, Andrews SR, Housain B, Alexander M, Mohamed M. Characterization of zaghrouta, an expression of happiness in the Middle East, a component of the differential diagnosis of psychogenic disorders. 2nd International Conference on Psychogenic Movement Disorders and Other Conversion Disorders. Apr 2008;78-79.
Brasic JR, Alexander M, Mohamed M. Differentiation of zaghrouta, an expression of happiness by women in the Middle East, from medical disease. Southern Medical Journal. Oct 2003;96(Suppl10):S35.
Jain S, Ferrando SJ. Manganese neurotoxicity presenting with depression, psychosis and catatonia. Psychosomatics. Jan-Feb 2011;52(1):74-7. [Medline].
Kumar S, Sur S, Singh A. Mega cisterna magna associated with recurrent catatonia: a case report. Biol Psychiatry. Aug 15 2011;70(4):e19. [Medline].
Spiegel DR, Varnell C Jr. A case of catatonia due to posterior reversible encephalopathy syndrome treated successfully with antihypertensives and adjunctive olanzapine. Gen Hosp Psychiatry. May-Jun 2011;33(3):302.e3-5. [Medline].
Brelinski L, Cottencin O, Guardia D, Anguill JD, Queyrel V, Hatron PY. Catatonia and systemic lupus erythematosus: a clinical study of three cases. Gen Hosp Psychiatry. Jan-Feb 2009;31(1):90-2. [Medline].
Kalivas KK, Bourgeois JA. Catatonia after liver and kidney transplantation. Gen Hosp Psychiatry. Mar-Apr 2009;31(2):196-8. [Medline].
Hsieh MH, Chen TC, Chiu NY, Chang CC. Zolpidem-related withdrawal catatonia: a case report. Psychosomatics. Sep-Oct 2011;52(5):475-7. [Medline].
Lahutte B, Cornic F, Bonnot O, Consoli A, An-Gourfinkel I, Amoura Z. Multidisciplinary approach of organic catatonia in children and adolescents may improve treatment decision making. Prog Neuropsychopharmacol Biol Psychiatry. Mar 7 2008;[Medline].
Larsen HH, Ritchie JC, McNutt MD, Musselman DL. Pulmonary embolism in a patient with catatonia: an old disease, changing times. Psychosomatics. Jul-Aug 2011;52(4):387-91. [Medline].
Sienaert P, Rooseleer J, De Fruyt J. Measuring catatonia: a systematic review of rating scales. J Affect Disord. Dec 2011;135(1-3):1-9. [Medline].
Bush G, Fink M, Petrides G, Dowling F, Francis A. Catatonia. I. Rating scale and standardized examination. Acta Psychiatr Scand. Feb 1996;93(2):129-36. [Medline].
Askenazy F, Dor E, Benoit M, Dupuis G, Serret S, Myquel M, et al. Catatonie chez une adolescente de 14 ans : traitement par clorazépam et carbamazépine et évolution à dix ans [Catatonia in a 14 year-old girl: Treatment with clonazepam and carbamazepine, a 10-year follow-up]. L'Encéphale. 2009.
Chang CH, Hsiao YL, Hsu CY, Chen ST. Treatment of catatonia with olanzapine: a case report. Prog Neuropsychopharmacol Biol Psychiatry. Nov 13 2009;33(8):1559-60. [Medline].
England ML, Ongür D, Konopaske GT, Karmacharya R. Catatonia in psychotic patients: clinical features and treatment response. J Neuropsychiatry Clin Neurosci. Spring 2011;23(2):223-6. [Medline].
Gupta A, Dhir A, Kumar A, Kulkarni SK. Protective effect of cyclooxygenase (COX)-inhibitors against drug-induced catatonia and MPTP-induced striatal lesions in rats. Pharmacol Biochem Behav. Dec 2009;94(2):219-26. [Medline].
Nomoto H, Hatta K, Usui C, Ito M, Kita Y, Arai H. Vitamin K deficiency due to prolongation of antibiotic treatment and decrease in food intake in a catatonia patient. Psychosomatics. Sep-Oct 2011;52(5):486-7. [Medline].
Chanpattana W, Kramer BA, Kunigiri G, Gangadhar BN, Kitphati R, Andrade C. A Survey of the Practice of Electroconvulsive Therapy in Asia. J ECT. May 13 2009;[Medline].
Chanpattana W. A survey of the practice of electroconvulsive therapy in Asia. European Psychiatry. 2009;24 Supplement 1:S770.
Wachtel LE, Kahng S, Dhossche DM, Cascella N, Reti IM. ECT for catatonia in an autistic girl. Am J Psychiatry. Mar 2008;165(3):329-33. [Medline].
Consoli A, Boulicot V, Cornic F, Fossati P, Barbeau M, Cohen D. Moderate clinical improvement with maintenance ECT in a 17-year-old boy with intractable catatonic schizophrenia. Eur Child Adolesc Psychiatry. Apr 2009;18(4):250-4. [Medline].
Slooter AJ, Braun KP, Balk FJ, et al. Electroconvulsive therapy for malignant catatonia in childhood. Pediatr Neurol. Mar 2005;32(3):190-2. [Medline].
Rhoads JC, Votolato NA, Young JL, Gilchrist RH. The successful use of right unilateral ultra-brief pulse electroconvulsive therapy in an adolescent with catatonia. Brain Stimulation. 2009.
Peralta V, Campos MS, de Jalon EG, Cuesta MJ. DSM-IV catatonia signs and criteria in first-episode, drug-naive, psychotic patients: psychometric validity and response to antipsychotic medication. Schizophr Res. May 2010;118(1-3):168-75. [Medline].
Van Den Eede F, Van Hecke J, Van Dalfsen A, Van den Bossche B, Cosyns P, Sabbe BG. The use of atypical antipsychotics in the treatment of catatonia. Eur Psychiatry. Aug 2005;20(5-6):422-9. [Medline].
Krivoy A, Weizman A, Kimchi-Nesher S, Zemishlany Z, Fischel T. Recurrnet [sic] catatonia: Fluctuating between psychotic and catatonic dimensions [abstract]. European Psychiatry. 2008;23:S328-S329.
Huang TL, Hung YY. Lorazepam reduces the serum brain-derived neurotrophic factor level in schizophrenia patients with catatonia. Prog Neuropsychopharmacol Biol Psychiatry. Feb 1 2009;33(1):158-9. [Medline].
Grover S, Aggarwal M. Long-term maintenance lorazepam for catatonia: a case report. Gen Hosp Psychiatry. Jan-Feb 2011;33(1):82.e1-3. [Medline].
Ostwald P. The "God of the dance": treating Nijinsky's manic excitement and catatonia. Hosp Community Psychiatry. Oct 1994;45(10):981-5. [Medline].
| Category | Causes |
| Neurologic conditions | Neuroleptic malignant syndrome[15] Administration of agents that block postsynaptic dopamine receptors* Administration of sibutramine,[16] withdrawn from US market October 8, 2010 Withdrawal of lorazepam and other sedatives Akinetic-rigid syndrome Arachnoid cyst in right parietal region Astrocytoma Atrophy of left amygdala[17] Autistic disorder[6, 7, 8, 18, 19, 20, 21, 22, 23] {{197} Basilar artery thrombosis Bilateral hemorrhagic lesions of temporal lobes Cerebellar catalepsy Cerebral hemorrhage Cerebral infarct Cerebrovascular disease Cortical venous thrombosis Central pontine myelinolysis Cortical basal ganglionic degeneration Dystonia Encephalitis (herpes, Trypanosoma cruzi) Encephalopathy (Borrelia burgdorferi, human immunodeficiency virus [HIV] infection, Wernicke encephalopathy) Familial fatal insomnia[24] Fibromuscular dysplasia with dissection of basilar artery Frontal lobotomy Head injury Huntington disease Hydrocephalus Hypopituitarism secondary to postpartum hemorrhage Idiopathic recurring stupor Inherited neurometabolic disorders Locked-in syndrome Meningitis, tuberculous Meningoencephalitis Multiple sclerosis[25, 26] Neurosyphilis Nonconvulsive status epilepticus Pervasive developmental disorders[7, 8, 22] Pallidoluysian atrophy Paraneoplastic encephalitis[27] Parkinsonism Postencephalitic parkinsonism Progressive multifocal leukoencephalopathy Progressive supranuclear palsy Schizencephaly Seizures (complex with partial symptomatology) Stiff-man syndrome Stroke Stupor Subarachnoid hemorrhage Subdural hematoma Substance intoxication (alcohol, disulfiram, organic fluorides, phencyclidine) Subthalamic mesencephalic tumor Surgical removal of cerebellar tumor Tay-Sachs disease Temporal lobe epilepsy Tuberous sclerosis Tumors (corpus callosum, glioma of third ventricle, supraventricular diffuse pinealoma) Vegetative state Von Economo encephalitis Wilson disease |
| Psychiatric conditions | Acute stress disorder Anorexia nervosa Autistic disorder[6] Brief reactive psychosis with catatonia Conversion disorder Hysteria Major depression, single episode with catatonic features Mood disorders Neuroleptic malignant syndrome[15] Posttraumatic stress disorder Schizophrenia Substance intoxication (3,4-methylenedioxymethamphetamine [ie, "ecstasy"], alcohol, amphetamine, phencyclidine, substance withdrawal, hypnotic-sedative, lorazepam) |
| Psychological factors | Immigration Experiencing rejection of an expression of love Feelings of alienation in an unfamiliar country |
| Medical conditions | Acquired immunodeficiency syndrome (AIDS) Acute intermittent porphyria Addison disease Bacterial septicemia Bronchorrhea Carcinoid tumors Diabetic ketoacidosis Encephalopathy (hepatic, HIV infection ? related, Wernicke) Fever of unknown cause Heat stroke Hepatic failure Hereditary coproporphyria Homocystinuria Hypercalcemia Hyperparathyroidism Hyperthyroidism Hyponatremia Hypothermia Intestinal atony Malaria Neuroleptic malignant syndrome[15] Poisoning (carbon monoxide, tetraethyl lead) Renal failure Substance intoxication (alcohol, cyclosporine, disulfiram, organic fluorides, phencyclidine) Syndrome of inappropriate antidiuretic hormone (SIADH) Syphilis Systemic lupus erythematosus Thermal injury Thrombotic thrombocytopenic purpura Tuberculosis Typhoid fever Uremia Von Economo encephalitis |
| Obstetric conditions | Hypopituitarism secondary to postpartum hemorrhage |
| *The administration of agents that block postsynaptic dopamine receptors is associated with the onset of catatonia in some individuals. | |

