Results 21 to 30 of about 76,774 (198)

What Is the Normal Trajectory of C‐Reactive Protein, Erythrocyte Sedimentation Rate, Plasma Fibrinogen and D‐Dimer after Two‐Stage Exchange for Periprosthetic Joint Infection?

Orthopaedic Surgery, Volume 14, Issue 11, Page 2987-2994, November 2022., 2022
A flow chart was shown for the included studies. Abbreviations: PJI: periprosthetic joint infection; THA, total hip arthroplasty; TKA, total knee arthroplasty. Objective C‐reactive protein (CRP), erythrocyte sedimentation rate (ESR), plasma fibrinogen and D‐Dimer are used as diagnostic biomarkers of prosthetic joint infection (PJI) after total joint ...
Yuangang Wu, Jinhan Zhou, Ran Liu, Yi Zeng, Kaibo Sun, Mingyang Li, Linbo Peng, Jiawen Xu, Bin Shen   +8 more
wiley   +1 more source

Haplotipos de la hemoglobina S: importancia epidemiológica, antropológica y clínica [PDF]

Revista Panamericana de Salud Pública, 1998
La relacion entre la drepanocitosis y los diferentes haplotipos del gen que codifica la subunidad betas de la globina ha permitido llegar a entender mejor las manifestaciones clinicas de aquella enfermedad. El uso de mejores tecnicas de laboratorio permite descartar la presencia de otros factores hereditarios capaces de ocultar el verdadero genotipo ...
Walter E. Rodríguez Romero, Germán F. Sáenz Renauld, Mario A. Chaves Villalobos   +2 more
openaire   +1 more source

Developing an emergency department order set to treat acute pain in sickle cell disease

Journal of the American College of Emergency Physicians Open, Volume 2, Issue 4, August 2021., 2021
Abstract Study Objective Patients with sickle cell disease (SCD) have many emergency department visits because of painful vaso‐occlusive episodes (VOE). Guidelines recommend treatment within 30 minutes of triage, but this is rarely achieved in clinical practice.
Yves Duroseau, David Beenhouwer, Michael S Broder, Bonnie Brown, Tartania Brown, Sarah N Gibbs, Kaedrea Jackson, Sally Liang, Melanie Malloy, Marie‐Laure Romney, Dana Shani, Jena Simon, Irina Yermilov   +12 more
wiley   +1 more source

PRÁTICAS EDUCATIVAS NA PROMOÇÃO DA ALIMENTAÇÃO ADEQUADA E SAUDÁVEL PARA AS PESSOAS COM DOENÇA FALCIFORME

Demetra, 2014
Sickle Cell Disease (SCD) is a chronic inherited disorder, characterized by the presence of abnormal erythrocytes containing S hemoglobin (HbS) that leads to diverse clinical complications and special nutritional needs.
Jorginete de Jesus Damião Trevisani, Marta Citelli dos Reis, Pilar Silva Raphael Mataratzis, Karen Cordovil, Ana Cecilia Freitas, Débora Lemos Lino, Juliana Omena, Cláudia dos Santos Cople-Rodrigues   +7 more
doaj   +1 more source

Association of serum selenium with anemia‐related indicators and risk of anemia

Food Science &Nutrition, Volume 9, Issue 6, Page 3039-3047, June 2021., 2021
Higher serum selenium is associated with an increased serum iron level, MCHC, and hemoglobin level and a decreased risk of anemia. Due to the narrow physiological range of selenium, the relationships between selenium‐ and anemia‐related indicators and risk of anemia were nonlinear.
Qing Zhou, Baozhu Zhang, Xi Chen, Qiuyan Chen, Lu Hao   +4 more
wiley   +1 more source

Evaluation of the Braden scale in predicting surgical outcomes in older patients undergoing major head and neck surgery

Laryngoscope Investigative Otolaryngology, Volume 6, Issue 1, Page 103-108, February 2021., 2021
Abstract Background Being able to predict negative postoperative outcomes is important for helping select patients for treatment as well for informed decision‐making by patients. Frailty measures are often time and resource intensive to use as screening measures, whereas the Braden scale, a commonly used measure to assess patients at risk of developing
Rajan Grewal, Michael C. Sklar, John R de Almeida, Wei Xu, Jie Su, Carissa M. Thomas, Shabbir M.H. Alibhai, David P Goldstein   +7 more
wiley   +1 more source

Beware the counsel of the oracle

, 2023
Journal of the American College of Emergency Physicians Open, Volume 4, Issue 5, October 2023.
Joshua A. Krieger, Robert Levine
wiley   +1 more source

Importância dos programas de triagem para o gene da hemoglobina S [PDF]

Revista Brasileira de Hematologia e Hemoterapia, 2007
A anemia falciforme caracteriza-se como quadro hemolitico hereditario que evolui cronicamente causando danos fisicos e emocionais as pessoas acometidas. Ate o presente momento nao se dispoe de tratamento curativo, a nao ser o transplante de medula ossea, que ainda tem sido realizado de maneira experimental.
Bandeira, Flávia M. G. C., Bezerra, Marcos A. C., Santos, Magnun N. N., Gomes, Yara M., Araújo, Aderson S., Abath, Frederico G. C.   +5 more
openaire   +3 more sources

Anemias ferropénicas asociadas a hemoglobinopatías en comunidades afrodescendientes en Colombia

NOVA, 2018
Objetivo. Determinar la presencia de anemias ferropénicas asociadas a hemoglobinopatías en afrodescendientes adultos colombianos habitantes de la ciudad de Tumaco,  en el Departamento  de Nariño y residentes de la localidad de Engativá, en Bogotá ...
Martha Castillo Bohórquez, Ana Isabel Mora Bautista, Ana Lucia Oliveros Rozo   +2 more
doaj   +1 more source

Aconselhamento genético do paciente com doença falciforme Genetic counseling in the sickle cell disease

Revista Brasileira de Hematologia e Hemoterapia, 2007
O aconselhamento genético é um componente importante da conduta médica na doença falciforme, apresentando relevantes implicações médicas, psicológicas, sociais, éticas e jurídicas.
Antonio Sérgio Ramalho, Luís Alberto Magna   +1 more
doaj   +1 more source