2024
Diagnosis and management of pyruvate kinase deficiency: international expert guidelines
Al-Samkari H, Shehata N, Lang-Robertson K, Bianchi P, Glenthøj A, Sheth S, Neufeld E, Rees D, Chonat S, Kuo K, Rothman J, Barcellini W, van Beers E, Pospíšilová D, Shah A, van Wijk R, Glader B, Mañú Pereira M, Andres O, Kalfa T, Eber S, Gallagher P, Kwiatkowski J, Galacteros F, Lander C, Watson A, Elbard R, Peereboom D, Grace R. Diagnosis and management of pyruvate kinase deficiency: international expert guidelines. The Lancet Haematology 2024, 11: e228-e239. PMID: 38330977, DOI: 10.1016/s2352-3026(23)00377-0.Peer-Reviewed Original ResearchExpert panelCountry of practiceCare of patientsEvidence-based guidelinesQuality of lifeClinical care of patientsPyruvate kinase deficiencySystematic literature searchDeficient careGuideline methodologistsPK deficiencyClinical careClinical guidelinesInternational expert guidelinesEstimated prevalenceHaemolytic anaemiaConsensus procedureManagement of chronic complicationsDraft recommendationsGRADE methodologyAGREE II frameworkExpert guidelinesLiterature searchClinical practiceInternational guidelines
2007
A Decline in the Frequency of Neonatal Exchange Transfusions and Its Effect on Exchange-Related Morbidity and Mortality
Steiner LA, Bizzarro MJ, Ehrenkranz RA, Gallagher PG. A Decline in the Frequency of Neonatal Exchange Transfusions and Its Effect on Exchange-Related Morbidity and Mortality. Pediatrics 2007, 120: 27-32. PMID: 17606558, DOI: 10.1542/peds.2006-2910.Peer-Reviewed Original ResearchConceptsExchange transfusionNeonatal exchange transfusionPatient demographicsDouble volume exchange transfusionSpecial care unit admissionsCare unit admissionRetrospective chart reviewSerious underlying conditionsUnit admissionIntravenous immunoglobulinAdverse eventsChart reviewCalcium replacementHigher proportionPlatelet transfusionsPostnatal careSingle institutionUnderlying conditionTransfusionPatientsClinical practiceAmerican AcademyUniform protocolSame time periodManagement guidelines
1999
Molecular diagnosis of hemoglobinopathies and other red blood cell disorders.
Arcasoy MO, Gallagher PG. Molecular diagnosis of hemoglobinopathies and other red blood cell disorders. Seminars In Hematology 1999, 36: 328-39. PMID: 10530715.Peer-Reviewed Original ResearchConceptsAppropriate prenatal counselingAppropriate patient educationRed blood cell disordersMolecular diagnosisBlood cell disordersClinical outcomesPatient educationRisk individualsCell disordersClinical practicePrenatal counselingRapid genetic diagnosisRapid diagnosisDiagnosisEarly detectionErythrocyte disordersRisk couplesDisordersPrenatal diagnosisGenetic diagnosisHemoglobinopathiesMolecular biology