Impact of ACGME-I Accreditation on Patient Outcomes at Hamad Medical Corporation: A Call for Evidence
Journal Title: Oman Medical Journal - Year 2019, Vol 34, Issue 1
Abstract
It is globally acknowledged that becoming a physician today brings complexities not faced in the past. There is growing evidence for new techniques in patient care as well as advancing technology that brings forth procedures never possible before.
Authors and Affiliations
Mohamad Abdul-Halim Chehab, Nagah Abdel-Aziz Selim
Keywords
Related Articles
- EP ID EP434830
- DOI 10.5001/omj.2019.15
- Views 87
- Downloads 0
Immunophenotypic Characteristics of T-Acute Lymphoblastic Leukemia in Omani Patients: A Correlation with Demographic Factors
Objectives: To study and classify the immunophenotypic characteristics of Omani patients diagnosed with T-cell acute lymphoblastic leukemia (T-ALL) and to correlate the results with age and gender as well as biological f...
Primary Hypothalamic Lymphoma in an Adult Male: A Case Report and Literature Review
Primary central nervous system lymphoma is a well-known entity. However, the hypothalamus is a rare location, especially in adults. Few cases of secondary lymphomas have been reported. We report a case of primary hypotha...
Autosomal Dominant Polycystic Kidney Disease and Pericardial Effusion
The autosomal dominant polycystic kidney disease (ADPKD) accounts for one out of 400–1000 live births, being a hereditary disorder with cystic and noncystic manifestations as well as extrarenal involvement. The pericardi...
Human Parvovirus B19 in Children with Sickle Cell Disease; Poking the Spleen
Parvovirus is a known culprit of transient red cell aplasia (TRCA) in children with sickle cell disease (SCD). Few reports have previously described the association between the virus and acute splenic sequestration crisi...
Neonatal Stridor in Familial Congenital Laryngeal Paralysis (Plott Syndrome): A Case Study in an Omani Family
Stridor presenting soon after birth due to bilateral abductor vocal cord paralysis (VCP) is rare. We report a family with bilateral VCP affecting four male members in two generations and hence suggesting X-linked recessi...