Results 31 to 40 of about 6,529,585 (334)

Diagnostic Errors in Pediatric Critical Care: A Systematic Review*

Pediatric Critical Care Medicine, 2021
Supplemental Digital Content is available in the text. OBJECTIVES: To summarize the literature on prevalence, impact, and contributing factors related to diagnostic error in the PICU. DATA SOURCES: Search of PubMed, EMBASE, and the Cochrane Library up to
Christina L. Cifra, J. Custer, Hardeep Singh, J. Fackler   +3 more
semanticscholar   +1 more source

Dataset from dried blood spot acylcarnitine for detection of Carnitine-Acylcarnitine Translocase (CACT) deficiency and Carnitine Palmitoyl Transferase 2 (CPT2) deficiency

Data in Brief, 2023
Clinical diagnosis of inborn errors of metabolism in the suspected patients is usually guided by the initial general investigations in the laboratory such as the concentration of ammonia, blood gases status, blood glucose and ketones.
Anasufiza Habib, Muhammad Irfan Bukhari Ahmad Nazri, Salina Abdul Rahman   +2 more
doaj   +1 more source

Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population

Molecular Genetics and Metabolism Reports, 2020
Introduction: Biotinidase deficiency (BD) is an autosomal recessively inherited disorder characterized by developmental delay, seizures, hypotonia, ataxia, skin rash/eczema, alopecia, conjunctivitis/visual problem/optic atrophy and metabolic acidosis ...
M. Mardhiah, Nor Azimah Abdul Azize, Yusnita Yakob, O. Affandi, Ngu Lock Hock, M.R. Rowani, Anasufiza Habib   +6 more
doaj   +1 more source

Patient and care partner assessments of diagnostic excellence in the emergency department: A cognitive interview study

International Journal of Nursing Studies Advances, 2023
Background: Diagnostic excellence encompasses both receiving an accurate and timely explanation of a health problem that was communicated well, and the process it took to get to the correct diagnosis.
Aaron A. Wiegand, Vadim Dukhanin, Natalia Gonzalez, Kathryn M. McDonald, Susan Peterson, Kelly T Gleason   +5 more
doaj   +1 more source

Meaningful Categorisation of Novice Programmer Errors [PDF]

, 2014
The frequency of different kinds of error made by students learning to write computer programs has long been of interest to researchers and educators. In the past, various studies investigated this topic, usually by recording and analysing compiler error
Kölling, Michael, McCall, Davin
core   +1 more source

Types of therapeutic errors in the management of osteoporosis made by physicians and medical students

BMC Medical Education, 2022
Background Clinical reasoning is of high importance in clinical practice and thus in medical education research. Regarding the clinical reasoning process, the focus has primarily been on diagnostic reasoning and diagnostic errors, but little research has
Olivia Tausendfreund, Leah T. Braun, Ralf Schmidmaier   +2 more
doaj   +1 more source

Hereditary Angioedema Due to C1-Inhibitor Deficiency in Romania: First National Study, Diagnostic and Treatment Challenges [PDF]

Iranian Journal of Immunology, 2020
Background: Hereditary angioedema (HAE) is a rare genetic potentially life-threatening disease characterized by episodic non-pruritic subcutaneous and submucosal edema attacks in different parts of the body.
Gabriella Gabos, Valentin Nadasan, Eniko Mihaly, Daniela Dobru   +3 more
doaj   +1 more source

Evidence-based decision support for pediatric rheumatology reduces diagnostic errors. [PDF]

, 2016
BACKGROUND: The number of trained specialists world-wide is insufficient to serve all children with pediatric rheumatologic disorders, even in the countries with robust medical resources. We evaluated the potential of diagnostic decision support software
Balu Athreya, CD Newgard, CK Correll, CL Deal, David Zurakowski, E Vittinghoff, Elizabeth Y. N. Ang, ES Berner, GD Schiff, Irit Tirosh, JE Allanson, JL McGhee, Jonathan S. Hausmann, JP Marcin, L Feldman, LL Minich, Lynn K. Feldman, M Al Maini, M Henrickson, M Henrickson, Mary Beth F. Son, Michael M. Segal, ML Mayer, MM Segal, MM Segal, O Wegwarth, P Ramnarayan, P Woo, R Tozzoli, Robert P. Sundel, SB Hanauef, WF Bond   +31 more
core   +2 more sources

First Universal Newborn Screening Program for Severe Combined Immunodeficiency in Europe. Two-Years' Experience in Catalonia (Spain)

Frontiers in Immunology, 2019
Severe combined immunodeficiency (SCID), the most severe form of T-cell immunodeficiency, can be screened at birth by quantifying T-cell receptor excision circles (TRECs) in dried blood spot (DBS) samples.
Ana Argudo-Ramírez, Andrea Martín-Nalda, Jose L. Marín-Soria, Rosa M. López-Galera, Sonia Pajares-García, Jose M. González de Aledo-Castillo, Mónica Martínez-Gallo, Marina García-Prat, Roger Colobran, Roger Colobran, Jacques G. Riviere, Yania Quintero, Tatiana Collado, Judit García-Villoria, Antonia Ribes, Pere Soler-Palacín   +15 more
doaj   +1 more source

Ebola US Patient Zero: lessons on misdiagnosis and effective use of electronic health records. [PDF]

, 2014
On September 30th, 2014, the Centers for Disease Control and Prevention (CDC) confirmed the first travel-associated case of US Ebola in Dallas, TX. This case exposed two of the greatest concerns in patient safety in the US outpatient health care system ...
Singh, Hardeep, Sittig, Dean, Upadhyay, Divvy   +2 more
core   +3 more sources