Læknablaðið : fylgirit - 03.01.2017, Qupperneq 64

Læknablaðið : fylgirit - 03.01.2017, Qupperneq 64
X V I I I V Í S I N D A R Á Ð S T E F N A H Í F Y L G I R I T 9 1 64 LÆKNAblaðið/Fylgirit 91 2017/103 V 4 Development of Drugs for Local Treatment of Oral Conditions Peter Holbrook1, Þórdís Kristmundsdóttir2 1Faculty of Odontology, UI, 2Faculty of Pharmaceutical Sciences, UI phol@hi.is Objectives: There is an unmet need for topical treatments of specific oral conditions, particularly in the oral mucosa. Methods: Medications commonly prescribed for oral mucosal ad- ministration are often intended for transdermal application. Many conditions affecting the oral mucosa require long-term treatments and some treatments are systemically applied. Clinical resistance and patient intolerance of such treatments may develop. There is thus a need to address these problems with drug development. Research at the University of Iceland has developed new formulations for topical treatments of oral mucosal conditions and carried out appropriate clinical trials. The main area of this research has been the inhibition of matrix metallo-proteina- se activity using topical doxycycline, initially in order to treat aphthous ulceration. The anti-microbial compound monocaprin was also tested for activity against herpes virus and, in combination with doxycycline, was developed in an active formulation for treating cold sores. Monocaprin also has anti-candidal activity that has been evaluated among geriatric patients with denture stomatitis. Results: Topical application of doxycycline was effective in promot- ing healing of mucosal lesions. Monocaprin reduced counts of Candida rapidly and significantly. Results of these clinical studies have been very promising when compared to the conventional treatments available. Conclusions: Stability of the active components has recently been effect- ively addressed and current research is aimed at different types of drug delivery systems in order to optimize drug delivery to the local mucosal site. This includes drug release time and muco-adhesive capacity of the formulation, thereby attempting to develop more disease-specific drug delivery systems. V 5 Association of fat mass-and obesity-associated (FTO) variant with stearoyl-CoA desaturase activity following a high-carbohydrate meal Harpa Óskarsdóttir1, Helgi Schiöth2, Guðrún Skúladóttir3 1Faculty of Medicine, Department of Physiology, 2Department of Neuroscience, Functional Pharmacology, 3Department of Physiology, University of Iceland hao17@hi.is Introduction: The human fat mass-and obesity-associated (FTO) gene has been associated with obesity, and data suggests that individuals homozy- gous for the FTO rs9939609 high-risk A allele weigh more on average than individuals homozygous for the FTO rs9939609 low-risk T allele. The exact mechanism of how it affects obesity has not been established. The enzyme stearoyl-CoA desaturase (SCD) plays an important role in the de novo lipogenic pathway, and its activity has been positively correlated with obesity. The aim of this study was to investigate the association between plasma SCD activity indices and rs9939609 variant of the FTO gene before and after a high-carbohydrate meal. Materials and methods: A total of 44 healthy individuals (median age 26 years, range 20-36) were divided into two groups, one homozygous for the FTO rs9939609 high-risk allele (AA; n=18), and another homozygous for the low-risk allele (TT; n=26). Fatty acid analysis was performed in plasma phospholipid samples from fasting individuals and again 2 hours following a high-carbohydrate breakfast to assess the SCD activity index (16:1n-7/16:0 ratio). The changes in SCD activity indices following a high- carbohydrate meal were compared between the two groups by F-test and unpaired Welch’s t-. Results: The SCD-16 activity index was significantly elevated (P < 0.05) following a high-carbohydrate breakfast in the AA group compared to the TT group. Conclusion: The results indicate that the SCD-16 activity index in subjects homozygous for the high-risk A allele is more affected than those homozy- gous for the low-risk T allele following a high-carbohydrate meal. V 6 Fast Diagnostic Track For Suspected Lung Cancer: A Patient Centered Approach Hrönn Harðardóttir1, Unnur A. Valdimarsdóttir2, Steinn Jónsson3 1School of Health Sciences, UI, 2Center for Public Health Sciences, UI , 3Landspitali – University Hospital hronnh@landspitali.is Introduction: A Fast Diagnostic Track (FDT) for patients with clinical or radiographic changes suggestive of lung cancer was launched at Landspít- ali, Iceland, in 2008. Patients go through 24-hours of diagnostic work-up, leading to a definite lung cancer diagnosis and staging. The aim of this study is to describe the clinical procedures and characteristics of patients going through the FDT. Material and methods: A retrospective study on 550 patients (mean age 68.1 years, 57% female) going through the FDT during 7 years from Febru- ary 1st 2008 - January 31st 2015. We further ascertained data on all pati- ents diagnosed with lung cancer in Iceland in 2014 (N=167, mean age 69.3 years, 61.7% female). Hospital ascertained information on background characteristics, diagnosis, staging, waiting-times and survival was collect- ed. Descriptive statistics and Cox proportional hazard-regression models were used for statistical analyses. Results: 426 of the FDT patients (77.5%) were diagnosed with lung cancer. The national proportion of patients receiving their lung cancer diagnosis through the FDT increased during the study period from 23% in 2008 to 48% in 2014. The median waiting time from referral to diagnosis was 10 days. One-year survival was 70.5% in the FDT group in comparison to 37.2% diagnosed outside the track in 2014; hazard ratio 1.60 (95% con- fidence interval: 0.95 – 2.71) when adjusting for age, sex, histology, stage at diagnosis and therapy. Conclusion: Increasing proportion of lung cancer diagnosis in Iceland is made through a fast diagnostic track with potential benefits for patient’s well-being and survival. V 7 Choice of analgesics in injectable form and reasons for the selection in hospitalised patients Hjördís B. Ólafsdóttir1, Pétur S. Gunnarsson1, Inga J. Arnardóttir2, Rannveig Einarsdóttir3 1Faculty of Pharmaceutical Sciences, 2Pharmacy, Landspitali – University Hospital, 3Division of finance, Landspitali – University Hospital psg@hi.is Introduction: Opioid analgesics are recommended in clinical guidelines for the treatment of pain. Strong opioid analgesics have similar efficacy, side effects and safety. This study examined the frequency of use and the reasons for the choice of opioids in injectable form in hospitalised patients at LSH. The use of guidelines or SOPs for the selection and administration of opioids was also reviewed. Methods: The study was retrospective and descriptive. Data about use
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