Results 101 to 110 of about 20,618 (233)

Is Cross‐Matching Required? Analysis of Blood Transfusion in Gynecological Surgeries at an Academic Hospital in Bangkok, Thailand: A Cross‐Sectional Study

Health Science Reports, Volume 9, Issue 4, April 2026.
ABSTRACT Background and Aims Effective utilization of perioperative blood transfusions can reduce costs and minimize blood waste. This study aimed to audit the appropriateness of current blood utilization practices in gynecological surgeries, characterize transfusion rates, and identify associated risk factors for transfusion.
Chutima Topipat, Punyanuch Chulnoul
wiley   +1 more source

Guidelines for the prevention of CMV transmisson by transfusion of blood components

Zdravniški Vestnik, 2013
Human cytomegalovirus can be transmitted by direct contact and iatrogenically by transfusion of blood components and by transplanted tissues or organs. After a primary, mostly asymptomatic infection, it remains latent in the body in CD34 + hematopoietic ...
Marko Cukjati, Vladan Rajić, Darja Paro Panjan, Irena Štucin Gantar, Mojca Grošelj Grenc, Urška Rahne Potokar, Samo Zver   +6 more
doaj  

Management of late-preterm and term infants with hyperbilirubinaemia in resource-constrained settings. [PDF]

, 2015
Hyperbilirubinaemia is a ubiquitous transitional morbidity in the vast majority of newborns and a leading cause of hospitalisation in the first week of life worldwide.
Boo, Nem-Yun, de Almeida, Maria Fernanda B, Iskander, Iman F, Kumar, Praveen, Ogunlesi, Tinuade A, Olusanya, Bolajoko O, Slusher, Tina M, Vaucher, Yvonne E   +7 more
core   +2 more sources

Association of re‐amniotomy in prelabor rupture of membranes at term and increased risk of cesarean delivery

International Journal of Gynecology &Obstetrics, Volume 173, Issue 1, Page 498-505, April 2026.
Abstract Objective To determine delivery outcomes in women diagnosed with prelabor rupture of membranes (PROM) who required re‐amniotomy. Methods This retrospective cohort study included 24 966 women with PROM at a single university‐affiliated tertiary medical center (2011–2023).
Roza Berkovitz‐Shperling, Roni Berin, Daniel Gabbai, Yariv Yogev, Shai Ram   +4 more
wiley   +1 more source

Successful management of severe hemolytic disease of the fetus and newborn (HDFN) due to anti-Kell

Journal of Perinatal Medicine
Hemolytic disease of the fetus and newborn (HDFN) is a potentially life-threatening condition, caused by maternal alloimmune antibodies targeting fetal red blood cells.
Hrastar Erika, Bricl Irena, Premru-Sršen Tanja, Gubenšek Jakob, Kornhauser Cerar Lilijana, Pečlin Polona   +5 more
doaj   +1 more source

Aftermath of the Hobby Lobby Decision: Implications for Women in the Workforce [PDF]

, 2016
Hobby Lobby is a chain of 640 arts and crafts stores owned by the Green family, based in Oklahoma City. This company is required to follow the Affordable Care Act (ACA), which mandates that larger employers—those with more than 50 employees—have to ...
Shah, Hirsh
core   +1 more source

A rare manifestation of neonatal alloimmune thrombocytopaenia [PDF]

, 2014
Neonatal alloimmune thrombocytopaenia (NAIT) results from a fetomaternal incompatibility with maternal sensitisation against a fetal human platelet antigen (HPA) and antibodies transfer to the fetal circulation, leading to platelet destruction.
Azenha, C, Jerónimo, M, Mesquita, J, Pereira, DF   +3 more
core   +1 more source

Molecular Testing in Sickle Cell Disease: From Newborn Screening to Transfusion Care

International Journal of Laboratory Hematology, Volume 48, Issue 2, Page 295-304, April 2026.
ABSTRACT Sickle cell disease (SCD) is one of the most frequent monogenic diseases worldwide and a highly heterogeneous and complex disease. SCD care carries several challenges. This includes early and accurate diagnosis as well as optimal red blood cell transfusion matching in this population carrying a high risk of alloimmunization.
Thomas Pincez, Yves D. Pastore
wiley   +1 more source

ACMG/AMP‐Based Variant Classification of a Novel HBA2 Variant (HBA2: C.297del, Hb Taiping) in Compound Heterozygosity With Hb Adana (HBA2:C.179G>A) Causing Non‐Deletional Hb H Disease

International Journal of Laboratory Hematology, Volume 48, Issue 2, Page 458-465, April 2026.
ABSTRACT Background Accurate classification of novel globin gene variants is critical for the diagnosis and management of thalassaemia. The adaptation of ACMG/AMP guidelines for globin genes represents an important step toward standardising variant interpretation and enhancing clinical utility in the field.
Norafiza Mohd Yasin, Suguna Somasundram, Syahzuwan Hassan, Nur Aisyah Aziz, Faidatul Syazlin Abdul Hamid, Ezzanie Suffya Zulkefli, Nor Nazuha Mohamad, Chin Ming Lee, Mohd Nazif Darawi, Thessalia Papasavva, Coralea Stephanou, Petros Kountouris, Sandra J. G. Arkesteijn, Tamara Koopman, Cornelis L. Harteveld   +14 more
wiley   +1 more source

Resolution of maternal Mirror syndrome after succesful fetal intrauterine therapy: a case series

BMC Pregnancy and Childbirth, 2018
Background Mirror syndrome (MS) is a rare obstetric condition usually defined as the development of maternal edema in association with fetal hydrops. The pathogenesis of MS remains unclear and may be misdiagnosed as pre-eclampsia.
Angel Chimenea, Lutgardo García-Díaz, Ana María Calderón, María Moreno-De Las Heras, Guillermo Antiñolo   +4 more
doaj   +1 more source