keyword
https://read.qxmd.com/read/38682958/transfusion-management-and-hemoglobin-based-oxygen-carrier-treatment-in-a-patient-with-anti-rh17-antibody
#1
Noah Mehr, Christine Fuja, Cody Simon, Timothy Carll, Rahaf Alkhateb, Sulin Wu, Anand A Patel, Fatima Aldarweesh
BACKGROUND: A 54-year-old Hispanic OPos female with known history of anti-Rh17 antibodies was diagnosed with Philadelphia-Chromosome positive (Ph+) acute lymphoblastic leukemia (ALL). Rh17, also known as Hr0 , is a high-frequency antigen composed of several epitopes on the RhCE protein. Anti-Rh17 antibodies can be made by individuals with missing or varied C/c, E/e antigens. Anti-Rh17 antibodies are clinically significant given multiple case reports of hemolytic disease of the fetus and newborn (HDFN)...
April 29, 2024: Transfusion
https://read.qxmd.com/read/38681455/unveiling-the-unlikely-extraskeletal-ewing-sarcoma-masquerading-as-gastrointestinal-bleeding
#2
Bryan M Greenfield, Madeleine A Wilson, Kyle J Schulte, Stephen Silverstein
While Ewing sarcoma is traditionally a malignant tumor of bone, it may uncommonly present extra-skeletally, leading to an array of puzzling presentations depending on the tissue involved. Here, we describe the case of a 66-year-old man who presented to the primary care office for evaluation of intermittent melena. He ultimately underwent capsule endoscopy and developed a secondary small bowel obstruction, unveiling his neoplasm. The tumor was then resected and managed with surveillance only, and the patient remains without evidence of disease after four years of follow-up...
March 2024: Curēus
https://read.qxmd.com/read/38681420/efficacy-and-safety-of-microsomal-ferric-pyrophosphate-supplement-for-iron-deficiency-anemia-in-pregnancy
#3
JOURNAL ARTICLE
Ankita Srivastav, Shilpa Kshirsagar, Tejasvini Adhav, Gayatri Ganu, Alok Shah
Introduction Anemia during pregnancy is characterized by decreased hemoglobin levels. Iron deficiency poses a significant global health concern, especially in pregnant women, where increased iron demands are crucial for both maternal and fetal well-being. Method In the current study, we investigated the effectiveness and safety of 30 mg SunActiveTM Fe (Taiyo GmbH, Yokkaichi, Japan), emulsified microsomalTM ferric pyrophosphate (EMFP) tablets in treating iron deficiency anemia in 27 second-trimester singleton pregnant women...
March 2024: Curēus
https://read.qxmd.com/read/38681383/sickle-cell-anomaly-meets-leukemic-challenge-a-case-report
#4
Shruti H Mandviya, Snehlata Hingway, Mayur Wanjari, Sukanya S Ingale, Isha Panbude, Atharvi Yembewar, Prachi Landge
This case report delves into the rare occurrence of sickle cell disease (SCD) and acute myeloid leukemia (AML) coexisting in a 36-year-old patient. The initial presentation, marked by escalating fatigue, pallor, and recurrent episodes initially attributed to sickle cell disease, unveiled an unexpected discovery of AML upon bone marrow examination. The diagnostic hurdles stemming from overlapping clinical features necessitated a thorough approach incorporating hematological, molecular, and imaging studies. Managing both conditions concurrently entailed navigating complexities addressed by a multidisciplinary team, tailoring chemotherapy regimens, and implementing personalized strategies to tackle complications associated with SCD...
March 2024: Curēus
https://read.qxmd.com/read/38681270/right-hepatic-artery-pseudoaneurysm-post-laparoscopic-cholecystectomy-a-case-report-of-endovascular-stent-graft-management
#5
Sohaib Ahmed, Rares Filep, Ahsan Mushtaq, Ovidiu Budisca
Gallstone-related diseases like cholelithiasis contribute significantly to global morbidity and mortality. Laparoscopic cholecystectomy (LC) is the gold standard for gallbladder removal but is associated with rare but severe complications, including hepatic artery pseudoaneurysms (PAs). A 72-year-old female presented with acute abdominal pain and upper gastrointestinal bleeding following a recent LC. Laboratory studies confirmed anemia with a hemoglobin level of 10 g/dL. Liver function tests were deranged, showing elevated alanine aminotransferase (ALT) at 209 U/L, aspartate aminotransferase (AST) at 472 U/L, total bilirubin levels at 3...
March 2024: Curēus
https://read.qxmd.com/read/38681037/hepatic-micro-abscesses-as-an-unusual-initial-presentation-of-systemic-lupus-erythematosus-a-case-report
#6
Sreethish Sasi, Mugahid Eltahir, Ezzeddin Ibrahim, Aishwariya Padmakumari, Jouhar Kolleri, Tasneem Abdallah, Ahmed Labib Shehatta, Nawal Hadwan, Hani Jaouni, Muna Al-Maslamani
KEY CLINICAL MESSAGE: Hepatic micro-abscesses can be a rare initial presentation of systemic lupus erythematosus (SLE). This case highlights the importance of considering autoimmune etiologies when infectious causes are ruled out and emphasizes the need for early recognition and appropriate treatment of atypical hepatic manifestations in SLE to achieve favorable outcomes. ABSTRACT: Systemic lupus erythematosus (SLE) is an autoimmune disease that affects multiple organs, including the liver...
May 2024: Clinical Case Reports
https://read.qxmd.com/read/38680759/pattern-of-clinical-and-laboratory-presentation-of-cerebral-malaria-among-children-in-nigeria
#7
JOURNAL ARTICLE
Tolulope O Jegede, Saheed B Oseni, John A O Okeniyi, Bankole Peter Kuti, Samuel A Adegoke, Qasim A Salau, Emmanuel Olaseinde Bello, Temitope Oyinlola Jegede, Abiodun John Kareem, Oyeku A Oyelami, Ibitoye Bayode Samuel, Korede O Oluwatuyi, Foluwakemi T Ekogiawe, Stanley E Obasohan, Ikechukwu S Abazu, Emmanuel O Babalola
INTRODUCTION: Cerebral malaria (CM) is the most lethal form of severe malaria with high case fatality rates. Overtime, there is an inherent risk in changing pattern of presentation of CM which, if the diagnosis is missed due to these changing factors, may portend a poor outcome. Variations in the pattern of clinic-laboratory presentations also make generalization difficult. This study was, therefore, set out to report the pattern of clinical and laboratory presentation of CM. METHODS: This was a cross-sectional study among children aged 6 months to 14 years admitted with a diagnosis of CM as defined by the World Health Organization criteria...
2024: Journal of Global Infectious Diseases
https://read.qxmd.com/read/38680699/application-and-management-of-continuous-glucose-monitoring-in-diabetic-kidney-disease
#8
EDITORIAL
Xin-Miao Zhang, Quan-Quan Shen
Diabetic kidney disease (DKD) is a common complication of diabetes mellitus that contributes to the risk of end-stage kidney disease (ESKD). Wide glycemic var-iations, such as hypoglycemia and hyperglycemia, are broadly found in diabetic patients with DKD and especially ESKD, as a result of impaired renal metabolism. It is essential to monitor glycemia for effective management of DKD. Hemoglobin A1c (HbA1c) has long been considered as the gold standard for monitoring glycemia for > 3 months. However, assessment of HbA1c has some bias as it is susceptible to factors such as anemia and liver or kidney dysfunction...
April 15, 2024: World Journal of Diabetes
https://read.qxmd.com/read/38679585/the-role-of-fetal-therapy-in-the-management-of-mirror-syndrome-a-narrative-review
#9
REVIEW
Nicole R Gavin, Alexandra D Forrest, Mara Rosner, Jena L Miller, Ahmet A Baschat
OBJECTIVES: Mirror syndrome (MS) is a condition characterized by the presence of maternal, fetal, and placental edema and is reversible through delivery or pregnancy termination. As fetal hydrops itself may be amenable to treatment, we sought to determine outcomes for MS primarily managed by fetal therapy through a narrative review of the literature and cases managed at our fetal center. STUDY DESIGN: PubMed, Embase, Web of Science, Scopus, and Google Scholar databases were searched through January 2024 using key words: mirror syndrome, Ballantyne's syndrome, fetal hydrops, maternal hydrops, pseudotoxemia, triple edema, maternal recovery, fetal therapy, and resolution...
December 2024: Journal of Maternal-fetal & Neonatal Medicine
https://read.qxmd.com/read/38678293/severe-bcg-immune-reconstitution-inflammatory-syndrome-lymphadenitis-successfully-managed-with-pre-antiretroviral-counseling-and-a-non-surgical-approach-a-case-report
#10
JOURNAL ARTICLE
Percina Machava, Winete Joaquim, Joseph Borrell, Shannon Richardson, Uneisse Cassia, Muhammad Sidat, Alice Maieca, Cláudia Massitela, Yara Quelhas, Cafrina Mucuila, Beatriz Elias, Massada da Rocha, H Simon Schaaf, W Chris Buck
BACKGROUND: Bacillus Calmette-Guérin (BCG) reactions are the most common cause of immune reconstitution inflammatory syndrome (IRIS) in HIV-positive infants who initiate antiretroviral therapy (ART). There is limited evidence regarding the incidence of BCG-IRIS; however, reports from outpatient cohorts have estimated that 6-9% of infants who initiated ART developed some form of BCG-IRIS within the first 6 months. Various treatment approaches for infants with BCG-IRIS have been reported, but there is currently no widely accepted standard-of-care...
April 27, 2024: AIDS Research and Therapy
https://read.qxmd.com/read/38673882/autoimmune-hemolytic-anemias-classifications-pathophysiology-diagnoses-and-management
#11
REVIEW
Melika Loriamini, Christine Cserti-Gazdewich, Donald R Branch
Autoimmune hemolytic anemias (AIHAs) are conditions involving the production of antibodies against one's own red blood cells (RBCs). These can be primary with unknown cause or secondary (by association with diseases or infections). There are several different categories of AIHAs recognized according to their features in the direct antiglobulin test (DAT). (1) Warm-antibody AIHA (wAIHA) exhibits a pan-reactive IgG autoantibody recognizing a portion of band 3 (wherein the DAT may be positive with IgG, C3d or both)...
April 12, 2024: International Journal of Molecular Sciences
https://read.qxmd.com/read/38673849/pharmacogenomics-of-drugs-used-in-%C3%AE-thalassemia-and-sickle-cell-disease-from-basic-research-to-clinical-applications
#12
REVIEW
Roberto Gambari, Aliyu Dahiru Waziri, Hemali Goonasekera, Emmanuel Peprah
In this short review we have presented and discussed studies on pharmacogenomics (also termed pharmacogenetics) of the drugs employed in the treatment of β-thalassemia or Sickle-cell disease (SCD). This field of investigation is relevant, since it is expected to help clinicians select the appropriate drug and the correct dosage for each patient. We first discussed the search for DNA polymorphisms associated with a high expression of γ-globin genes and identified this using GWAS studies and CRISPR-based gene editing approaches...
April 12, 2024: International Journal of Molecular Sciences
https://read.qxmd.com/read/38673453/diagnosis-treatment-and-long-term-management-of-vitamin-b12-deficiency-in-adults-a-delphi-expert-consensus
#13
JOURNAL ARTICLE
Rima Obeid, Emmanuel Andrès, Richard Češka, Babak Hooshmand, Rosa-Maria Guéant-Rodriguez, Gabriel Ioan Prada, Jarosław Sławek, Latchezar Traykov, Binh Ta Van, Tamás Várkonyi, Karlheinz Reiners, The Vitamin B Consensus Panelists Group
Background/Objectives : Vitamin B12 deficiency can cause variable symptoms, which may be irreversible if not diagnosed and treated in a timely manner. We aimed to develop a widely accepted expert consensus to guide the practice of diagnosing and treating B12 deficiency. Methods : We conducted a scoping review of the literature published in PubMed since January 2003. Data were used to design a two-round Delphi survey to study the level of consensus among 42 experts. Results : The panelists agreed on the need for educational and organizational changes in the current medical practices for diagnosing and treating B12 deficiency...
April 10, 2024: Journal of Clinical Medicine
https://read.qxmd.com/read/38670490/management-of-peri-surgical-anemia-in-elective-surgery-conclusions-and-recommendations-according-to-delphi-ucla-methodology
#14
JOURNAL ARTICLE
V Moral, A Abad Motos, C Jericó, M L Antelo Caamaño, J Ripollés Melchor, E Bisbe Vives, J A García Erce
INTRODUCTION: Preoperative anemia affects approximately one third of surgical patients. It increases the risk of blood transfusion and influences short- and medium-term functional outcomes, increases comorbidities, complications and costs. The "Patient Blood Management" (PBM) programs, for integrated and multidisciplinary management of patients, are considered as paradigms of quality care and have as one of the fundamental objectives to correct perioperative anemia. PBM has been incorporated into the schemes for intensified recovery of surgical patients: the recent Enhanced Recovery After Surgery 2021 pathway (in Spanish RICA 2021) includes almost 30 indirect recommendations for PBM...
April 24, 2024: Revista española de anestesiología y reanimación
https://read.qxmd.com/read/38669810/spontaneous-rectus-sheath-hematoma-revealed-by-abdominal-pain-during-pregnancy-a-case-report
#15
Bacem Zaidi, Wael Gazzah, Mehdi Ben Saad, Sihem Sindi, Walid Maraach, Zied Mensi
INTRODUCTION AND IMPORTANCE: Rectus sheath hematoma (RSH) is an uncommon but significant cause of acute abdominal pain in pregnancy, challenging in both diagnosis and treatment. It often arises from ruptured epigastric vessels and is associated with factors like anticoagulation therapy and previous abdominal surgery. Misdiagnosis, due to nonspecific symptoms, frequently leads to unnecessary surgeries, posing substantial risks to maternal and fetal health. CASE PRESENTATION: We present a case of a 32-year-old multiparous woman at 31 weeks of gestation, experiencing right-sided abdominal pain and irregular contractions...
April 24, 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38669382/management-of-diabetes-mellitus-patients-with-sickle-cell-anemia-challenges-and-therapeutic-approaches
#16
REVIEW
Emmanuel Ifeanyi Obeagu, Getrude Uzoma Obeagu
The coexistence of diabetes mellitus (DM) and sickle cell anemia (SCA) poses significant challenges in clinical management due to the complex interactions and overlapping complications associated with both conditions. Managing diabetes in individuals with SCA requires a comprehensive approach that addresses the unique physiological and pathological aspects of both diseases. This paper reviews the challenges encountered in the management of DM in patients with SCA and explores therapeutic strategies and approaches to optimize patient care...
April 26, 2024: Medicine (Baltimore)
https://read.qxmd.com/read/38669341/modified-delphi-panel-consensus-recommendations-for-management-of-severe-aplastic-anemia
#17
JOURNAL ARTICLE
Daria V Babushok, Amy E DeZern, Carlos de Castro, Zora R Rogers, David Beenhouwer, Michael S Broder, Suzanne Fanning, Sarah N Gibbs, Rabi Hanna, Jaroslaw P Maciejewski, Bart L Scott, Srinivas K Tantravahi, Marcin W Wlodarski, Irina Yermilov, Bhumika J Patel
Severe aplastic anemia (SAA) is a rare hematologic condition for which there is no clear management algorithm. A panel of 11 adult and pediatric experts on aplastic anemia was assembled and, using the RAND/UCLA modified Delphi panel method, evaluated >600 varying patient care scenarios to develop clinical recommendations for the initial and subsequent management of patients of all ages with SAA. Here we present the panel's recommendations to rule out inherited bone marrow failure (IBMF) syndromes, on supportive care prior to and during first-line therapy, and on first-line (initial management) and second-line (subsequent management) therapy of acquired SAA, focusing on when transplant versus medical therapy is most appropriate...
April 26, 2024: Blood Advances
https://read.qxmd.com/read/38668714/do-you-bleed-a-1-year-fobt-case-series-study
#18
JOURNAL ARTICLE
Spyridon Zouridis, Daniel Sofia, Osama Alshakhatreh, Madeline Cleary, Omar Daghstani, Paul J Feustel, Maheep Sangha, Seth Richter
GOALS: The goal of this study is to investigate fecal occult blood test's (FOBT) usage in cases of suspected gastrointestinal bleeding and how it may affect hospitalization length and inpatient endoscopy procedures. BACKGROUND: FOBT is an approved modality used in colorectal cancer screening but is often used inappropriately for the investigation of suspected gastrointestinal bleeding (GIB) in the hospital setting. The efficiency of FOBT when used for this purpose is questionable...
April 29, 2024: Journal of Clinical Gastroenterology
https://read.qxmd.com/read/38668287/dengue-associated-hemophagocytic-lymphohistiocytosis-a-narrative-review-of-its-identification-and-treatment
#19
REVIEW
Kay Choong See
Dengue's lack of specific treatments beyond supportive care prompts a focus on uncovering additional pathophysiological factors. Dengue-associated hemophagocytic lymphohistiocytosis (HLH), characterized by dysregulated macrophage activation and cytokine storm, remains underexplored despite its potential to worsen disease severity and mortality. While rare, dengue-associated HLH disproportionately affects severe cases, significantly impacting mortality rates. To mitigate high mortality, early identification and familiarity with dengue-associated HLH are imperative for prompt treatment by clinicians...
April 17, 2024: Pathogens
https://read.qxmd.com/read/38667514/respiratory-complications-are-the-main-predictors-of-1-year-mortality-in-patients-with-hip-fractures-the-results-from-the-alzira-retrospective-cohort-study
#20
JOURNAL ARTICLE
Elisa García-Tercero, Ángel Belenguer-Varea, Daniela Villalon-Ruibio, Jesús López Gómez, Rodrigo Trigo-Suarez, Cristina Cunha-Pérez, Miguel Germán Borda, Francisco Jose Tarazona-Santabalbina
Introduction : Hip fractures pose a significant challenge for older individuals given their high incidence and one-year mortality rate. The objective of this study was to identify the primary predictors of one-year mortality in older adults hospitalized for hip fractures. Methods: We conducted a retrospective cohort study involving adults aged 70 years or older who were admitted to the hospital for fragility hip fractures between 1 January 2014 and 31 December 2021. A total of 3229 patients were recruited, with 846 (26...
April 9, 2024: Geriatrics
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