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1.
Reviews in Clinical Medicine [RCM]. 2015; 2 (3): 151-157
in English | IMEMR | ID: emr-175655

ABSTRACT

Morphine is one of the most potent alkaloid in opium, which has substantial medical uses and needs and it is the first active principle purified from herbal source. Morphine has commonly been used for relief of moderate to severe pain as it acts directly on the central nervous system; nonetheless, its chronic abuse increases tolerance and physical dependence, which is commonly known as opiate addiction. Morphine withdrawal syndrome is physiological and behavioral symptoms that stem from prolonged exposure to morphine. A majority of brain regions are hypofunctional over prolonged abstinence and acute morphine withdrawal. Furthermore, several neural mechanisms are likely to contribute to morphine withdrawal. The present review summarizes the literature pertaining to neural mechanisms underlying morphine withdrawal. Despite the fact that morphine withdrawal is a complex process, it is suggested that neural mechanisms play key roles in morphine withdrawal

2.
Acta Medica Iranica. 2013; 51 (7): 482-486
in English | IMEMR | ID: emr-138260

ABSTRACT

Any suboptimum treatment in the management of patients can lead to medication errors [MEs] that may increase morbidity and mortality in hospitalized individuals. By establishing well-designed patient care activities within the managed care setting, clinical pharmacists can cooperate with other health care professionals to provide quality care and maximize safety. The aim of this study was to evaluate the frequency and prevention of MEs by clinical pharmacists. This was a cross-sectional interventional study conducted in internal wards of a teaching hospital during a two-month period. During this period, patient records, and physician orders were reviewed by clinical pharmacists. Any prescription error identified was documented. Incorrect drug selection, dose, dosage form, frequency, or route of administration all were considered as medication errors. Then, the clinical pharmacist discuss about findings with the clinical fellows to change faulty orders. The frequency and types of MEs in different wards that were detected and prevented by clinical pharmacists was documented. During the study period, in 132 patients, 262 errors were detected [1.98 per each]. Wrong frequency 71 [27%], forget to order 37 [14.1%], wrong selection 33 [12.5%], drug interactions 26 [9.9%], forget to discontinue 25 [9.5%] and inappropriate dose adjustment in renal impairment 25 [9.5%] were the most types of errors. Cardiovascular medications were the class with the highest detected errors [31.6%] followed by gastrointestinal agents [15.6%]. Medication errors are common problems in medical wards that their frequency can be restricted by the intervention of clinical pharmacists


Subject(s)
Humans , Female , Male , Pharmacists , Hospitals, Teaching , Cross-Sectional Studies , Drug Interactions
3.
IJPM-International Journal of Preventive Medicine. 2013; 4 (5): 517-522
in English | IMEMR | ID: emr-138487

ABSTRACT

It is believed that paraoxonase-2 gene polymorphism is associated with type 2 diabetes. This study is aimed to investigate the association between paraoxonase-2 gene polymorphism and type 2 diabetes in an Iranian population. This study was performed on 200 individuals including 100 diabetics and 100 healthy subjects. Genomic DNA was extracted from peripheral blood leukocytes, and PCR-RFLP was carried out. Palindromic sequence in PON2 gene was recognized by Dde1 restriction endonuclease. In order to visualize restriction products, electrophoresis was carried out using polyacrylamide gel [8%] and ethidium bromide staining. The expected PCR product of 331 bp was obtained. Digestion of this product with DdeI showed four Ser homozygotes, three Cys homozygotes, and five Ser311 Cys heterozygotes. The gene frequency of Cys [C] in diabetic subjects was significantly higher than in healthy subjects. This study suggests that an association exists between Ser311 Cys polymorphism and type 2 diabetes mellitus


Subject(s)
Humans , Diabetes Mellitus, Type 2/genetics , Polymorphism, Genetic , Genetic Predisposition to Disease , Gene Frequency , DNA Restriction Enzymes , Genetic Association Studies , Polymerase Chain Reaction
4.
IJPR-Iranian Journal of Pharmaceutical Research. 2012; 11 (1): 151-156
in English | IMEMR | ID: emr-131722

ABSTRACT

Drug Utilization Evaluation [DUE] studies facilitate assessing the appropriateness and rational use of medications.The goal of the present study was to evaluate Amphotericin B usage in neutropenic patients. A prospective DUE study was performed in Hematology-Oncology and Stem Cell Transplantation wards at Taleghani hospital for one-year. National comprehensive cancer network, clinical practice guidelines in oncology, American Hospital Formulary Service and other relevant medical practice and up-to dated articles were used to evaluate whether Amphotericin B is properly used according to the guidelines. All data collected by a pharmacist in daily review using information of physician and nursing records as well as laboratory findings. During the one-year study, 35 patients receiving amphotericin B were evaluated. 29 patients [82.9%] received amphotericin B due to neutropenia and fever and 6 patients had confirmed fungal infections. All of the injectable solutions of amphotericin B were appropriately prepared for intravenous infusion. In addition, for all patients, ordering [indication] of the study drug was in accordance with the guidelines. Twenty-five [71.4%] patients received an appropriate dose according to the guidelines. Duration of treatment was properly selected in 21 [60%] patients. Twenty-two [62.8%] patients developed hypokalemia as the most frequent adverse drug event. Although, preparation and indication of amphotericin B was in compliance with the current guidelines, dosage and duration of treatment were considered to be incoherent with the designed protocol used in this study. We conclude more attention should be paid to dosage and duration of treatment with amphotericin B in order to optimize its administration

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