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1.
J Clin Pharm Ther ; 37(2): 212-6, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21501204

RESUMO

WHAT IS KNOWN AND OBJECTIVES: Several studies have reported that use of the Hartford nomogram in different patients' population was associated with low serum gentamicin concentrations (SGC) at different intervals or midpoints. This study was intended to determine the prevalence and predictors of SGC in patients with sickle cell disease (SCD) as another population representing low SGC while utilizing the Hartford protocol. METHODS: This retrospective observational study was carried out in a University-teaching hospital in Oman. The study was conducted from January 2005 through May 2008 and included all adult patients with SCD admitted during that time. Four-hundred and seven SGC representing 248 SCD patients were evaluated. The serum gentamicin concentration was considered sub-optimal if it was <2µg/mL (baseline of Hartford nomogram). Analyses were performed using univariate and multivariate statistical techniques. RESULTS AND DISCUSSION: Eighty-three percent (n=339) of SGC were sub-optimal. Multivariate analysis using logistic regression revealed that sub-optimal SGC were associated with younger patients with higher creatinine clearance. Specifically, patients who were ≤23years old were twice more likely to have sub-optimal SGC compared with those who were >23years of age (95% CI: 1·14-3·45; P=0·015). Patients with creatinine clearance of ≥200mL/min were 5·20 times more likely to have sub-optimal SGC compared with those with creatinine clearance <200mL/min (95% CI: 1·81-14·49; P=0·002). Furthermore, the logistic model also demonstrated that higher serum urea was associated with low SGC, with each one unit increase in serum urea, patients were 17% less likely to have sub-optimal SGC (95% CI: 0·72-0·96; P=0·011). Additionally, patients who were on piperacillin±tazobactam therapy given concurrently with gentamicin were 53% less likely to have sub-optimal SGC (95% CI: 0·28-0·83; P=0·009). WHAT IS NEW AND CONCLUSION: A majority of patients with SCD had sub-optimal SGC. The pharmacokinetic profile of such patients is apparently too variable to fit the existing Hartford protocol. The Hartford nomogram should be modified to address this issue. Otherwise, clinicians should revert to multiple daily dosing.


Assuntos
Anemia Falciforme/complicações , Antibacterianos/farmacocinética , Infecções Bacterianas/tratamento farmacológico , Gentamicinas/farmacocinética , Adolescente , Adulto , Fatores Etários , Antibacterianos/administração & dosagem , Antibacterianos/uso terapêutico , Infecções Bacterianas/etiologia , Creatinina/sangue , Creatinina/urina , Feminino , Gentamicinas/administração & dosagem , Gentamicinas/uso terapêutico , Hospitais Universitários , Humanos , Modelos Logísticos , Masculino , Análise Multivariada , Nomogramas , Omã , Prevalência , Estudos Retrospectivos , Adulto Jovem
2.
J Obstet Gynaecol ; 27(2): 150-4, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17454461

RESUMO

A retrospective study was conducted over a 10-year period on 32,000 maternities at Abha General Hospital, Abha, Saudi Arabia, to estimate the contribution of eclampsia and severe pre-eclampsia to maternal mortality and morbidity and also fetal wastage. It included 18 cases of eclampsia and 297 cases of severe pre-eclampsia. Multiple regression analysis revealed that only the presence of prodromal symptoms significantly affected the occurrence of eclampsia, p < 0.05, while nulliparous patients were a high risk group for eclampsia. Maternal complications including eight cases of massive ascites occurred exclusively in severe pre-eclamptics. Although no maternal deaths were reported, the perinatal mortality rate was 16.6% and 14.1% among the eclamptics and severe pre-eclamptic patients, mainly from prematurity. Regarding the eclamptic patients, 17(94.4%) had the first fit before arrival at the hospital, 13(72.2%) before labour, while 3(16.6%) had fits before and during labour and 1(5.6%) had the fits after delivery. Suggestions are proffered to reducing maternal morbidity and perinatal mortality and morbidity.


Assuntos
Eclampsia/mortalidade , Pré-Eclâmpsia/mortalidade , Adolescente , Adulto , Feminino , Maternidades , Humanos , Mortalidade Infantil , Recém-Nascido , Mortalidade Materna , Pessoa de Meia-Idade , Gravidez , Estudos Retrospectivos , Arábia Saudita/epidemiologia
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