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1.
J Med Case Rep ; 13(1): 45, 2019 Feb 27.
Article in English | MEDLINE | ID: mdl-30808405

ABSTRACT

INTRODUCTION: Gastric pharmacobezoars are a rare entity that can induce mechanical gastric outlet obstructions and sometimes prolong toxic pharmacological effects. Certain medications, such as sustained-release forms, contain cellulose derivatives that may contribute to the adhesion between pills and lead to the creation of an aggregate resulting in a pharmacobezoar. Case reports are rare, and official guidelines are needed to help medical teams choose proper treatment options. CASE PRESENTATION: Our patient was a 40-year-old Caucasian woman with borderline personality disorder and active suicidal thoughts who was found unconscious after a massive drug consumption of slow-release clomipramine, lorazepam, and domperidone. On her arrival in the emergency room, endotracheal intubation was preformed to protect her airway, and a chest x-ray revealed multiple coffee grain-sized opaque masses in the stomach. She was treated with activated charcoal followed by two endoscopic gastric decontaminations 12 h apart in order to extract a massive gastric pharmacobezoar by manual removal of the tablets. CONCLUSION: This case demonstrates that in the case of a massive drug consumption, a pharmacobezoar should be suspected, particularly when cellulose-coated pills are ingested. Severe poisoning due to delayed drug release from the gastric aggregate is a potential complication. Detection by x-ray is crucial, and treatment is centered on removal of the aggregate. The technique of decontamination varies among experts, and no formal recommendations exist to date. It seems reasonable that endoscopic evaluation should be performed in order to determine the appropriate technique of decontamination. Care should be patient-oriented and take into account the clinical presentation and any organ failure, and it should not be determined solely by the suspected medication ingested. Thus, serum levels are not sufficient to guide management of tricyclic antidepressant intoxication.


Subject(s)
Antidepressive Agents, Tricyclic/poisoning , Bezoars/chemically induced , Clomipramine/poisoning , Delayed-Action Preparations/poisoning , Domperidone/poisoning , Drug Overdose/pathology , Lorazepam/poisoning , Adult , Antidepressive Agents, Tricyclic/pharmacokinetics , Bezoars/pathology , Charcoal/therapeutic use , Clomipramine/pharmacokinetics , Delayed-Action Preparations/pharmacokinetics , Domperidone/pharmacokinetics , Drug Overdose/complications , Endoscopy , Female , Humans , Lorazepam/pharmacokinetics , Suicide, Attempted , Treatment Outcome
2.
Hum Exp Toxicol ; 37(4): 343-349, 2018 Apr.
Article in English | MEDLINE | ID: mdl-28425352

ABSTRACT

BACKGROUND: Accidental drug overdose is a common problem in young children. We examined the influence of formulation and dose in enquiries for different gastro-oesophageal reflux disease treatments in children under 5 years to the UK's National Poisons Information Service. METHODS: Overdose characteristics with ranitidine, omeprazole or domperidone were compared with those of metoclopramide and the H-1 antagonist chlorphenamine, for the period 1 July 2007 to 30 June 2015. RESULTS: There were a total of 1092 ranitidine, 618 domperidone and 1193 omeprazole cases; 669, 281 and 424, respectively, were single agent enquiries; of these 77% (517) of ranitidine, 52% (145) domperidone and 32% (135) omeprazole cases occurred in children <5 years. In comparison, 17% (34/424) of metoclopramide and 53% (533/1013) of chlorphenamine were <5 years; 79% (410/517) of ranitidine overdose enquiries in children <5 years were under 6 months of age, higher than domperidone (68/145, 47%; p < 0.05), omeprazole (8/135, 6%), chlorphenamine (13/553, 2%) or metoclopramide (1/34, 3%) (all p < 0.01). In children aged <6 months, 101 were 10-fold overdoses, 86 with ranitidine. CONCLUSIONS: Tenfold overdoses in children (<5 years) were a feature of ranitidine enquiries, likely due to the high concentration of the syrup. This has relevance to other liquid formulations used for non-licenced indications in young children. Such therapeutic errors cause significant carer anxiety and healthcare utilization. Assistance is needed from manufacturers and legislators in modifying formulation so that drugs can be safely used in young children. Education of prescribers and carers is also needed to reduce the incidence of such errors that cause significant carer anxiety and healthcare utilization.


Subject(s)
Drug Overdose/epidemiology , Gastrointestinal Agents/poisoning , Poison Control Centers , Ranitidine/poisoning , Age Factors , Child, Preschool , Chlorpheniramine/administration & dosage , Chlorpheniramine/poisoning , Databases, Factual , Domperidone/administration & dosage , Domperidone/poisoning , Drug Compounding , Drug Overdose/diagnosis , Female , Gastrointestinal Agents/administration & dosage , Humans , Incidence , Infant , Male , Metoclopramide/administration & dosage , Metoclopramide/poisoning , Omeprazole/administration & dosage , Omeprazole/poisoning , Ranitidine/administration & dosage , Risk Factors , United Kingdom/epidemiology
3.
Pediatr Med Chir ; 12(2): 205-6, 1990.
Article in Italian | MEDLINE | ID: mdl-2235667

ABSTRACT

Domperidone is useful in the treatment of vomiting and gastroesophageal reflux in children. Its efficaciousness is due to the antagonist effect on gastrointestinal dopaminergic receptors. Contrary to the initial expectations, domperidone is able to penetrate into the hematoencephalic barrier and to cause adverse neurologic reactions. We report a case of extrapyramidal reaction in a child after moderate overdosage of domperidone.


Subject(s)
Basal Ganglia Diseases/chemically induced , Domperidone/poisoning , Humans , Infant , Male , Syndrome
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