8 results on '"Al Abri Z"'
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2. Voltage Stability Analysis of Muscat Power System During Summer Weather Conditions
- Author
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Ellithy, K., primary, Gastli, A., additional, Al-Alawi, S., additional, Al-Hinai, A., additional, and Al-Abri, Z., additional
- Published
- 2000
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3. Economics of primary healthcare: cost estimation of clinical services at primary care facilities in the six countries of the Gulf Cooperation Council.
- Author
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Elmusharaf K, Poix S, Grafton D, Jung JS, Gribble R, Stanton R, Mahmoud L, Al Asfoor DH, Alawadi T, Mustafa M, Shuwaiter L, Alsuwaidan MS, Al-Abri Z, Al-Sabahi S, Fadda S, Syed HR, Almutairi M, Al-Farsi YM, Banatvala N, and Tarlton D
- Subjects
- Humans, Middle East, Health Care Costs statistics & numerical data, Primary Health Care economics
- Abstract
Objective: While the Gulf Cooperation Council (GCC) countries have demonstrated a strong commitment to strengthening primary healthcare (PHC), the costs of delivering these services in this region remain relatively unexplored. Understanding the costs of PHC delivery is essential for effective resource allocation and health system efficiency., Design: We used an ingredient-based method to estimate the cost of delivering a selection of services at PHC facilities in the six GCC countries in 2019. Services were categorised into eight programmes: immunisation; non-communicable diseases (NCDs); oral and dental care; child health; nutrition; mental health; reproductive, maternal, neonatal and child health and general practice. The cost estimation focused on two key ingredients: the costs of drugs and supplies and the healthcare workforce cost. The coverage rates of specific types of health services, including screening and mental health services, were also estimated. Data for the analysis were obtained from ministries of health, health statistics reports, online databases, national surveys and scientific literature., Results: The estimated costs of delivering the selected services at public PHC facilities in the six GCC countries totalled US$5.7 billion in 2019, representing 0.34% of the combined 2019 GDP. The per capita costs varied from US$69 to US$272. General practice and NCD programmes constituted 79% of the total costs modelled while mental health ranged between 0.0% and 0.3%. Over 8 million individuals did not receive NCD screening services, and over 30 million did not receive needed mental health services in public PHC facilities across the region., Conclusions: To our knowledge, this is the first study to estimate the costs of services delivered at PHC facilities in the GCC countries. Identifying the main cost drivers and the services which individuals did not receive can be used to help strengthen PHC to improve efficiency and scale up needed services for better health outcomes., Competing Interests: Competing interests: The authors alone are responsible for the views expressed in this article, and they do not necessarily represent the views, decisions or policies of the institutions with which they are affiliated., (© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
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- 2024
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4. Medical Students' Clinical Knowledge of Integrated Management of Childhood Illness: A cross-sectional comparative study.
- Author
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Al Abri Z, Al Kiyumi M, Jaju S, and Al Saadoon M
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- Humans, Cross-Sectional Studies, Female, Male, Oman, Surveys and Questionnaires, Adult, Health Knowledge, Attitudes, Practice, Clinical Clerkship methods, Child, Students, Medical statistics & numerical data, Students, Medical psychology, Clinical Competence statistics & numerical data, Clinical Competence standards
- Abstract
Objectives: This study aimed to investigate and compare the clinical knowledge implications of the integrated management of childhood illness (IMCI) preservice education between pre-clerkship and junior clerkship medical students., Methods: This observational comparative cross-sectional study was conducted between June and August 2022 at Sultan Qaboos University, Muscat, Oman. A self-administered questionnaire was utilised and included questions on sociodemographic data, duration of IMCI preservice training, knowledge of the participants concerning the IMCI objectives and information on a range of childhood conditions., Results: A total of 97 medical students were included in the study. The majority of students (42.3%) had received 2 lectures in IMCI preservice training. The role of the IMCI approach in reducing childhood morbidity and mortality was advocated by the majority of students (80.8% in the junior-clerkship [JCR] group and 73.3% in the pre-clerkship group). The awareness of the IMCI component of improving the health system was higher in JCR compared to pre-clerkship participants ( P = 0.044). When compared to pre-clerkship students, the JCR participants demonstrated a slightly higher awareness of skin pinch ( P = 0.038), chest indrawing ( P = 0.008), anaemia assessment based on nail bed examination ( P = 0.002), diagnostic assessment of malnutrition based on palm examination ( P = 0.018), sucking capacity in breastfeeding ( P = 0.025), and vaccines such as those for tuberculosis ( P = 0.001), pneumococcal ( P = 0.018) and rotavirus ( P = 0.007)., Conclusion: The majority of students displayed good IMCI knowledge and JCR students showed better knowledge compared to pre-clerkship candidates., Competing Interests: CONFLICTS OF INTEREST: The authors declare no conflict of interest., (© Copyright 2024, Sultan Qaboos University Medical Journal, All Rights Reserved.)
- Published
- 2024
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5. A Rare Case of Heterotopic Ossification of the Patella Tendon in an Adolescent Presenting with Tendon Rupture.
- Author
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Supreeth S, Al-Barwani A, Al Habsi I, Al Ghanami S, Al Abri Z, and Al-Adawi K
- Abstract
Heterotopic ossification is the abnormal formation of mature, lamellar bone in nonosseous tissue such as tendons, ligaments, muscles, and soft tissue. We discuss a rare case of a young adolescent with patellar tendon rupture postheterotopic ossification. A 13-year-old male presented to us with knee pain and inability to extend for 6 weeks following trivial trauma. Preliminary radiological investigations revealed a high riding patella with ossification in the patella tendon. The magnetic resonance scan confirmed the same with patellar tendon disruption and heterogeneous ossification. He underwent surgery with patella tendon repair, augmentation with autograft, and had complete recovery at 6 months' follow-up., Competing Interests: Conflict of Interest None declared., (The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ).)
- Published
- 2020
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6. Synthesis of novel (R)-4-fluorophenyl-1H-1,2,3-triazoles: A new class of α-glucosidase inhibitors.
- Author
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Avula SK, Khan A, Halim SA, Al-Abri Z, Anwar MU, Al-Rawahi A, Csuk R, and Al-Harrasi A
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- Drug Design, Humans, Molecular Docking Simulation, Molecular Structure, Structure-Activity Relationship, Glycoside Hydrolase Inhibitors chemical synthesis, Glycoside Hydrolase Inhibitors pharmacology, Triazoles chemistry, alpha-Glucosidases chemistry
- Abstract
Diabetes is a non-communicable disease, which occurs either due to the lack of insulin or the inability of the human body to recognize it. The recent data indicates an increase in the trend of people diagnosed with Type 2 diabetes mellitus (T2DM). α-Glucosidase inhibitors are known to reduce the impact of carbohydrates on blood glucose level and prevent the digestion of carbohydrates. α-glucosidase inhibitors hold great potential for the treatment of T2DM. In search of better α-glucosidase inhibitors, a series of novel (R)-4-fluorophenyl-1H-1,2,3-triazole derivatives were synthesized (6 and 8a-n) and evaluated for their α-glucosidase inhibitory activity in vitro. All new compounds were characterized by
1 H NMR,13 C NMR,19 F NMR, ESI-MS, and where applicable by single crystal X-ray diffraction (8 m). A preliminary structure-activity relationship suggested that the presence of 1H-1,2,3-triazole ring in (R)-4-fluorophenyl-1H-1,2,3-triazole derivatives has remarkable contribution in the overall activity. Molecular docking studies were carried out to investigate the binding mode of compounds within the active site of the α-glucosidase enzyme. Docking results are in complete agreement with the experimental finding. This study unravelled a new class of triazole derivatives with α-glucosidase inhibitory activity., (Copyright © 2019 Elsevier Inc. All rights reserved.)- Published
- 2019
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7. Synthesis of 1H-1,2,3-triazole derivatives as new α-glucosidase inhibitors and their molecular docking studies.
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Avula SK, Khan A, Rehman NU, Anwar MU, Al-Abri Z, Wadood A, Riaz M, Csuk R, and Al-Harrasi A
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- Dose-Response Relationship, Drug, Glycoside Hydrolase Inhibitors, Humans, Molecular Structure, Structure-Activity Relationship, Triazoles chemical synthesis, Triazoles chemistry, Molecular Docking Simulation, Triazoles pharmacology, alpha-Glucosidases metabolism
- Abstract
Inhibition of α-glucosidase is an effective strategy for controlling the post-prandial hyperglycemia in diabetic patients. For the identification of new inhibitors of this enzyme, a series of new (R)-1-(2-(4-bromo-2-methoxyphenoxy) propyl)-4-(4-(trifluoromethyl) phenyl)-1H-1,2,3-triazole derivatives were synthesized (8a-d and 10a-e). The structures were confirmed by NMR, mass spectrometry and, in case of compound 8a, by single crystal X-ray crystallography. The α-glucosidase inhibitory activities were investigated in vitro. Most derivatives exhibited significant inhibitory activity against α-glucosidase enzyme. Their structure-activity relationship and molecular docking studies were performed to elucidate the active pharmacophore against this enzyme. Compound 10b was the most active analogue with IC
50 value of 14.2 µM, while compound 6 was found to be the least active having 218.1 µM. A preliminary structure-activity relationship suggested that the presence of 1H-1,2,3-triazole ring in 1H-1,2,3-triazole derivatives is responsible for this activity and can be used as anti-diabetic drugs. The molecular docking studies of all active compounds were performed, in order to understand the mode of binding interaction and the energy of this class of compounds., (Copyright © 2018 Elsevier Inc. All rights reserved.)- Published
- 2018
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8. New α-Glucosidase inhibitors from the resins of Boswellia species with structure-glucosidase activity and molecular docking studies.
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Ur Rehman N, Khan A, Al-Harrasi A, Hussain H, Wadood A, Riaz M, and Al-Abri Z
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- Catalytic Domain, Glycoside Hydrolase Inhibitors isolation & purification, Glycoside Hydrolase Inhibitors pharmacokinetics, Molecular Docking Simulation, Molecular Structure, Saccharomyces cerevisiae enzymology, Structure-Activity Relationship, Triterpenes isolation & purification, Triterpenes pharmacokinetics, alpha-Glucosidases chemistry, Boswellia chemistry, Glycoside Hydrolase Inhibitors chemistry, Resins, Plant chemistry, Triterpenes chemistry
- Abstract
Phytochemical investigation of the oleo-gum resins from Boswellia papyrifera afforded one new triterpene, named 3α-hydroxyurs-5:19-diene (1) together with twelve known compounds including eight triterpenoids (2-9), two diterpenoids (10 and 11) and two straight chain alkanes (12 and 13). Similarly ten more known compounds were isolated from the resin of Boswellia sacra including one triterpene (20) and nine boswellic acids (14-19 and 21-23). Herein the compound 2 was first time reporting from natural source along with complete NMR assignment, while compounds 3-11 are known, but reported for the first time from the resin of B. papyrifera. The structure elucidation was done by advance spectroscopic
1 D and2 D NMR techniques viz.,1 H,13 C, DEPT, HSQC, HMBC, and COSY, and NEOSY, ESI-MS and compared with the reported literature. All compounds were evaluated for their α-glucosidase inhibitory activity and as result eight of them 1, 3, 10, 11, 15, and 17-19 were found significantly active against α-glucosidase with an IC50 value ranging from 15.0 ± 0.84 to 80.3 ± 2.33 µM, while 21 exhibited moderate activity with IC50 of 799.9 ± 4.98 µM. Furthermore, two compounds 24 and 25 were synthesised from 16 and 17 to see the effect of carboxyl group in structural-activity relationship (SAR) study. Compounds 24 and 25 retained good α-glucosidase inhibition as compared to 16 and 17, indicating that carboxylic group play a key role in SAR. In addition, the aforementioned activity of all the active compounds was first time reported for their α-glucosidase inhibition potential. The molecular docking studies showed that all the active compounds well accommodate in the active site of the enzyme. Moreover pharmacokinetic properties of the compounds were predicted in silico, suggesting that the compounds possess drug like properties and excellent ADMET profile., (Copyright © 2018 Elsevier Inc. All rights reserved.)- Published
- 2018
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