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1.
J Clin Psychiatry ; 62 Suppl 2: 12-6, 2001.
Article in English | MEDLINE | ID: mdl-11232745

ABSTRACT

Acute, high-dose loading strategies (rapid neuroleptization) with the first-generation antipsychotics administered orally or parenterally, alone or combined with benzodiazepines, have been a commonly used treatment paradigm for controlling acutely agitated psychotic patients. The rationale was to achieve high plasma levels of drug within a shorter time period, resulting in rapid symptom mitigation. However, studies have shown that rapid neuroleptization with first-generation antipsychotics is associated with a greater incidence of side effects. To our knowledge, loading strategies with second-generation antipsychotics have not been investigated, primarily owing to a need for dose titration. Olanzapine, a second-generation antipsychotic, is well tolerated in doses ranging from 5 to 20 mg. The objective of this report was to determine experience with the use of up to 20 mg of an oral loading dose of olanzapine administered within 4 hours in the treatment of patients early in an acute psychotic phase of their illness. In the reported case series of 57 patients, olanzapine initiated at 15 to 20 mg/day was a safe and effective medication for rapidly calming the agitation of acutely agitated psychotic patients (rapid tranquilization). Furthermore, dose reduction over 2 to 3 weeks was achieved in a number of patients without appreciable loss of efficacy.


Subject(s)
Antipsychotic Agents/therapeutic use , Pirenzepine/analogs & derivatives , Pirenzepine/therapeutic use , Psychotic Disorders/drug therapy , Acute Disease , Antipsychotic Agents/administration & dosage , Antipsychotic Agents/adverse effects , Basal Ganglia Diseases/chemically induced , Basal Ganglia Diseases/epidemiology , Benzodiazepines , Drug Administration Schedule , Humans , Incidence , Olanzapine , Pirenzepine/administration & dosage , Pirenzepine/adverse effects , Psychiatric Status Rating Scales/statistics & numerical data , Psychotic Disorders/psychology
2.
Can Fam Physician ; 45: 2656-60, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10587773

ABSTRACT

OBJECTIVE: To highlight recent empirical evidence for effective interventions that can guide family physicians in managing patients after suicide attempts. QUALITY OF EVIDENCE: Randomized control trials of psychosocial interventions for people after suicide attempts have provided some evidence for effective interventions. MAIN MESSAGE: Suicide attempts are more common than suicides; the number of attempts seen in a family practice is estimated to be 10 to 15 yearly. Up to two thirds of patients who take their lives by suicide have seen a family physician in the month before their death. Principles of care after a suicide attempt include actively engaging the patient, involving the family, restricting access to means of suicide, and developing intervention plans to deal with the psychopathology that has placed the patient at risk. CONCLUSIONS: Family physicians have a crucial role in preventing suicide through aftercare and ongoing monitoring of patients who have attempted suicide.


Subject(s)
Patient Care Team , Suicide Prevention , Suicide, Attempted/prevention & control , Adolescent , Adult , Aged , Family Practice , Female , Humans , Male , Middle Aged , Randomized Controlled Trials as Topic , Recurrence , Risk Factors , Suicide/psychology , Suicide, Attempted/psychology , Treatment Outcome
3.
Eur J Biochem ; 266(2): 347-51, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10561574

ABSTRACT

The gene coding for rat heart fatty acid-binding protein (FABP), along with 1.2 kb of its 5'-untranscribed region, was amplified by PCR, cloned and sequenced. As in other FABP genes, the coding sequence is interrupted by three introns of 3.4, 1.4 and 1.1 kb, respectively. Fluorescence in situ hybridization mapping revealed that the gene is located on chromosome 5q36. Using intron-specific primers flanking exon 2, unspliced primary transcript RNA of the FABP gene was detected in a preparation of total RNA isolated from rat heart, proving that the cloned gene is expressed in adult cardiac tissue.


Subject(s)
Carrier Proteins/chemistry , Carrier Proteins/genetics , Neoplasm Proteins , Nerve Tissue Proteins , 5' Untranslated Regions , Animals , Base Sequence , Carrier Proteins/biosynthesis , Chromosome Mapping , Cloning, Molecular , Exons , Fatty Acid-Binding Protein 7 , Fatty Acid-Binding Proteins , In Situ Hybridization, Fluorescence , Introns , Male , Models, Genetic , Molecular Sequence Data , Myocardium/metabolism , RNA, Messenger/metabolism , Rats , Rats, Wistar , Reverse Transcriptase Polymerase Chain Reaction
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