Table of Contents

HOW TO TREAT SCHIZOAFFECTIVE DISORDER 2025
GUIDELINES FOR THE DIAGNOSIS AND TREATMENT OF COMMON MENTAL DISORDERS
(Enacted under Decision No. 2058/QĐ-BYT dated May 14, 2020, by the Minister of Health)
Article 17
SCHIZOAFFECTIVE DISORDER
CHIEF EDITOR
Associate Professor, PhD Nguyễn Trường Sơn
CO-EDITOR
Associate Professor, PhD Lương Ngọc Khuê
PhD Nguyễn Doãn Phương
CONTRIBUTING AUTHORS
PhD Trần Thị Hà An
MSc Trịnh Thị Vân Anh
PhD Vũ Thy Cầm
MSc Trần Mạnh Cường
PhD Nguyễn Văn Dũng
PhD Vương Ánh Dương
PhD Lê Thị Thu Hà
MSc Trần Thị Thu Hà
MSc Phạm Công Huân
MSc Đoàn Thị Huệ
Specialist Doctor II Nguyễn Thị Minh Hương
MSc Vũ Thị Lan
- Nguyễn Phương Linh
Specialist Doctor II Nguyễn Thị Phương Loan
MSc Bùi Văn Lợi
MSc Nguyễn Thị Phương Mai
PhD Trần Nguyễn Ngọc
MSc Bùi Nguyễn Hồng Bảo Ngọc
MSc Trương Lê Vân Ngọc
MSc Bùi Văn San
PhD Dương Minh Tâm
MSc Phạm Xuân Thắng
MSc Lê Thị Phương Thảo
MSc Lê Công Thiện
MSc Vương Đình Thủy
Associate Professor, PhD Nguyễn Văn Tuấn
Specialist Doctor II Ngô Văn Tuất
MSc Đặng Thanh Tùng
MSc Vũ Sơn Tùng
MSc Cao Thị Ánh Tuyết
MSc Nguyễn Thị Ái Vân
Specialist Doctor II Hồ Thu Yến
MSc Nguyễn Hoàng Yến
CONTRIBUTORS TO EVALUATION AND FEEDBACK
Associate Professor, PhD Nguyễn Thanh Bình
PhD Vũ Thy Cầm
PhD Nguyễn Hữu Chiến
Specialist Doctor II Võ Thành Đông
PhD Lê Thị Thu Hà
Specialist Doctor II Đỗ Huy Hùng
PhD Nguyễn Mạnh Hùng
MSc Nguyễn Trọng Khoa
Specialist Doctor II Ngô Hùng Lâm
Associate Professor, PhD Phạm Văn Mạnh
Specialist Doctor II Trần Ngọc Nhân
PhD Dương Minh Tâm
MSc Đặng Duy Thanh
PhD Vương Văn Tịnh
Specialist Doctor II Lâm Tứ Trung
PhD Lại Đức Trường
PhD Cao Văn Tuân
Associate Professor, PhD Nguyễn Văn Tuấn
SECRETARIAT TEAM
MSc Đặng Thanh Tùng
MSc Trương Lê Vân Ngọc
BA Đỗ Thị Thư
Article 17
SCHIZOAFFECTIVE DISORDER
I. DEFINITION
Schizoaffective disorder is characterized by prominent emotional symptoms (mania, depression) and schizophrenic symptoms occurring simultaneously or within a few days of each other during the same episode. The disorder progresses in episodes, with periods of remission between episodes, and has a tendency toward chronicity.
II. ETIOLOGY
The precise cause and pathogenesis of schizoaffective disorder remain unclear. It is classified as an endogenous disorder influenced by multiple factors, including genetics, immunity, and toxicity.
III. DIAGNOSIS
- Diagnostic Criteria
Schizoaffective disorder meets the full criteria for a moderate to severe mood disorder (F30, F31, F32) alongside schizophrenic symptoms persisting for at least 2 weeks, including at least one of the following:
- Thought Echo, Insertion, or Broadcasting:Hearing thoughts aloud, feeling thoughts imposed or stolen.
- Delusions of Control or Passivity: Beliefs of being controlled or influenced.
- Hallucinatory Voices: Commentary or discussions about the patient, or voices from body parts.
- Persistent, Culturally Inappropriate Delusions:Implausible beliefs.
- Incoherent or Neologistic Speech:Irrelevant or invented language.
- Catatonic Behavior: Posturing, waxy flexibility, negativism.
– Symptoms must not be attributable to organic brain disease or substance-induced psychosis.
- Clinical Subtypes (ICD-10)
– Schizoaffective Disorder, Manic Type:
– Meets general criteria for schizoaffective disorder.
– Meets criteria for mania (F30.1 or F31.1).
– Schizoaffective Disorder, Depressive Type:
– Meets general criteria for schizoaffective disorder.
– Meets criteria for moderate to severe depression (F31.3, F31.4, F32.1, or F32.2).
– Schizoaffective Disorder, Mixed Type:
– Meets general criteria for schizoaffective disorder.
– Meets criteria for bipolar mixed episode (F31.6).
– Other/Unspecified Schizoaffective Disorder:
- Differential Diagnosis
– Schizophrenia: Features characteristic psychotic symptoms (delusions, hallucinations) without simultaneous typical mood symptoms (depression, mania).
– Bipolar Disorder with Psychotic Features: Prominent mood symptoms (depression, mania) without typical schizophrenic psychotic symptoms.
- Ancillary Testing
4.1. Basic Labs
– Blood: Hematology, biochemistry, microbiology (HIV, HBV, HCV).
– Urine: General analysis, drug screening, syphilis serology.
4.2. Imaging/Functional Tests
– Chest X-ray, abdominal ultrasound.
– EEG, ECG, cerebral blood flow, transcranial Doppler.
– CT/MRI brain (select cases).
4.3. Psychological Assessments
– PANSS (Positive and Negative Symptom Scale).
– Personality: EPI, MMPI.
– Others: BDI, Zung, HDRS, HARS, HAD, MMSE.
IV. TREATMENT
- Treatment Principles
– Early detection and treatment, focusing on pharmacotherapy and psychotherapy.
– Pharmacotherapy is key, combined with psychotherapy, occupational therapy, and social reintegration.
– Start with monotherapy; if response is poor, use combination therapy.
– Monitor drug use closely to manage side effects promptly.
– Educate families/communities to reduce stigma and foster collaboration with healthcare providers.
– Address relapse triggers; maintain treatment post-acute phase with community monitoring.
- Treatment Framework
– Pharmacotherapy alongside psychotherapy and community rehabilitation.
- Specific Treatments
3.1. Pharmacotherapy
– Antipsychotics: 1-3 agents (prefer monotherapy; switch or combine up to 3 if ineffective):
– Typical:
– Chlorpromazine (25 mg tabs/vials; 50-250 mg/24h).
– Levomepromazine (25 mg tabs; 25-250 mg/24h).
– Haloperidol (1.5-5 mg tabs, 5 mg vials; 5-30 mg/24h).
– Thioridazine (50 mg tabs; 100-300 mg/day).
– Atypical:
– Amisulpride (50-400 mg tabs; 200-800 mg/24h).
– Clozapine (25-100 mg tabs; 50-800 mg/24h).
– Risperidone (1-2 mg tabs; 1-12 mg/24h).
– Olanzapine (5-10 mg tabs; 5-60 mg/24h).
– Quetiapine (50-300 mg tabs; 600-800 mg/day).
– Aripiprazole (5-30 mg tabs; 10-30 mg/day).
– Antidepressants: 1-3 agents (prefer monotherapy; switch or combine up to 3 if ineffective):
– SSRIs:
– Fluoxetine (20 mg; 10-40 mg/day).
– Paroxetine (20 mg; 20-60 mg/day).
– Sertraline (50 mg; 50-200 mg/day).
– Fluvoxamine (100 mg; 100-300 mg/day).
– Escitalopram (10-20 mg; 10-20 mg/day).
– Citalopram (10-60 mg/day).
– Dual-Acting:
– Venlafaxine (37.5 mg; 75-225 mg/day).
– Mirtazapine (30 mg; 30-60 mg/day).
– Tricyclics:
– Amitriptyline (25 mg; 50-100 mg/day).
– Clomipramine (25 mg; 50-75 mg/day).
– Imipramine (10-150 mg/day).
– Other: Tianeptine (12.5-50 mg/day).
– Mood Stabilizers: 1-2 agents (prefer monotherapy; switch or combine up to 2 if ineffective):
– Valproate (200-2500 mg/day).
– Divalproex (750 mg/day to 60 mg/kg/day).
– Carbamazepine (400-1200 mg/day).
– Oxcarbazepine (1200-2400 mg/day).
– Lamotrigine (100-400 mg/day).
– Topiramate (50-400 mg/day).
– Gabapentin (300-1800 mg/day).
– Treatment by Subtype:
– Depressive Type: Combine antipsychotics and antidepressants.
– Adjuncts: Benzodiazepines (diazepam, lorazepam, bromazepam, alprazolam), non-benzodiazepines (etifoxine, zopiclone), beta-blockers (propranolol), mood stabilizers (valproate, divalproex, lamotrigine), neuroprotectants (piracetam, ginkgo biloba, vinpocetine, choline alfoscerate, nicergoline), nutrition (B vitamins, minerals, IV feeding), hepatic support, cognitive enhancers.
– Manic Type: Combine antipsychotics and mood stabilizers.
– Adjuncts: Benzodiazepines, non-benzodiazepines, beta-blockers, neuroprotectants, nutrition, hepatic support, cognitive enhancers.
– Mixed Type: Combine antipsychotics and mood stabilizers.
– Adjuncts: Benzodiazepines, non-benzodiazepines, beta-blockers, antidepressants (SSRIs, SNRIs, mirtazapine), neuroprotectants, nutrition, hepatic support, cognitive enhancers.
– Monitoring:
– Side Effects:
– Extrapyramidal symptoms: Cholinesterase inhibitors (trihexyphenidyl, benztropine), beta-blockers, sedatives.
– Neuroleptic malignant syndrome/serotonin syndrome: Early detection, ICU management.
– Metabolic disorders: Monitor BMI, blood tests every 3-6 months.
– Clozapine: White blood cell count every 3 months.
– Tardive dyskinesia: Muscle relaxants, sedatives, vitamin E, anticholinergics.
3.2. Psychotherapy
– Individual, family, or group therapy to support patients through psychological crises, enhance illness insight, stabilize family dynamics, and aid community reintegration.
3.3. Electroconvulsive Therapy (ECT) and Transcranial Magnetic Stimulation (TMS)
– ECT: Effective for catatonia, suicidal behavior due to depression, treatment-resistant delusions/hallucinations, or agitation.
– TMS: Useful for persistent auditory hallucinations or depression.
3.4. Occupational and Rehabilitation Therapy
– Start activities at the patient’s capability level to rebuild confidence, gradually increasing intensity without causing stress.
– Tailor vocational rehabilitation to socio-economic-cultural context.
3.5. Physical Therapy and Community Management
– Ongoing monitoring and treatment in the community.
V. PROGNOSIS AND COMPLICATIONS
– Risk increases with a family history of schizophrenia, schizoaffective disorder, or bipolar disorder.
– Suicide is a significant potential complication.
VI. PREVENTION
– Exact cause unknown, so prevention focuses on:
– Fostering independence and adaptability to life’s challenges.
– Reducing stress through sharing and coping strategies.
– Monitoring individuals with a family history of schizophrenia or related disorders for early detection and treatment.
– Post-discharge follow-up, sustained specialist treatment, avoiding overexertion/stress, and proactive management of physical illnesses to prevent relapse.
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