Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Adicionar filtros








Intervalo de ano
1.
Pakistan Journal of Medical Sciences. 2017; 33 (2): 498-501
em Inglês | IMEMR | ID: emr-187925

RESUMO

Objective: To ascertain patients and physician views regarding hazard and compliance of oral liquid Vitamin D glass ampoule and tablets


Methods: This cross sectional survey was conducted from November 1st 2016 to 15th December 2016. Patients who were prescribed Vitamin D glass ampoule from oral route in last three months were included along with physicians who routinely prescribe vitamin D after taking informed consent. The participants were asked about injuries related to the use of glass ampoule, ease of using this from, after taste preference of tablet or injectable form as well as demography. Data was analysed with SPSS version 24.0


Results: Total 182 patients were included in the study with mean +/- SD age of 39.4 +/- 12.4 years. Majority of patients, 80.2% [142] said they prefer oral tablet in preference to injectable ampule in oral form if given choice while prescribing Vitamin D. Moreover 66.7% [64] doctors prefer to prescribe tablet form of Vitamin D instead of injection as oral form for vitamin D deficiency among their patients. One third of patients, 33% [n=59] sustained injury while breaking the ampule which included minor self-controlled bleeding by glass particles in 50% [n=35]. Less than half of doctors 46.9% [n=45] said they taught their patients about usage of injectable Vitamin D ampules


Conclusion: Majority of patients prefer Vitamin D tablet instead of Oral liquid in glass ampoule if they got the choice among two. The results of this study provide important implications for our doctors about patients concern of hazard, after taste and compliance with orally administered Vitamin D glass ampoules

2.
PAFMJ-Pakistan Armed Forces Medical Journal. 2017; 67 (5): 808-812
em Inglês | IMEMR | ID: emr-191437

RESUMO

Objective: To evaluate the protective effects of melatonin on cisplatin-induced nephrotoxicity in rabbits. Study Design: Laboratory based randomized control trial. Place and Duration of Study: Department of Pharmacology and Therapeutics in collaboration with Clinico Pathologic Laboratory, Army Medical College, Rawalpindi, from Apr to Jun 2015


Material and Methods: Eighteen rabbits were divided into three groups, each consisting of six rabbits. Baseline serum urea, creatinine, sodium and potassium were measured. Rabbits were weighed for dose calculation. A single dose of cisplatin 10mg/kg was given as I/P injection to the toxic group. The protective group received 5 mg/kg I/P melatonin for three days. Rabbits were sacrificed 72 hours after the cisplatin dose and both kidneys were sent for histopathology. Statistical analysis was carried out by using Microsoft Office Excel 2010 and SPSS version 21. Student's t-test and one way ANOVA, followed by 'Post Hoc Tukey' test was used for biochemical parameters, while Chi Square' test was used for histopathological comparison


Results: Moderate nephrotoxicity [grade-II] was seen in the toxic group, with substantial elevations of serum urea and creatinine [p<0.001], and serum sodium and potassium [p<0.01]. Melatonin ameliorated the renal injury


Conclusion: The protective effects of melatonin on cisplatin-induced nephrotoxicity were due to its antioxidant properties

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA