4.7 Article

Nephrological Complications in Hemoglobinopathies: SITE Good Practice

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Oncology

Incidence of cancer and related deaths in hemoglobinopathies: A follow-up of 4631 patients between 1970 and 2021

Raffaella Origa et al.

Summary: This study evaluated the relationship between hemoglobinopathies and malignant tumors. The findings suggest that the overall risk of cancer is not increased in patients with hemoglobinopathies, but hepatocellular carcinoma remains the most frequent tumor. The recent stability in the incidence of hepatocellular carcinoma may be explained by advancements in treatment.

CANCER (2023)

Article Hematology

Overall and complication-free survival in a large cohort of patients with β-thalassemia major followed over 50 years

Gian Luca Forni et al.

Summary: We present data on survival and complications in a cohort of 709 transfusion-dependent beta-thalassemia major patients in Italy. Overall survival probability at 30 years was 83.6%, with better survival in the younger birth cohort and in females. The most common disease-related causes of death were heart disease and bone marrow transplant complications. Survival continues to improve with access to care, best practice sharing, research, and collaboration between centers.

AMERICAN JOURNAL OF HEMATOLOGY (2023)

Review Urology & Nephrology

The nephropathy of sickle cell trait and sickle cell disease

Kenneth Ataga et al.

Summary: Sickle cell syndromes are associated with kidney abnormalities and nephropathy. The pathophysiology of SCD-related nephropathy is multifactorial, including oxidative stress, hyperfiltration, and glomerular hypertension. Patients with SCD experience faster decline in kidney function and often present with albuminuria. Multiple genetic modifiers are also implicated in the development and progression of SCD-related nephropathy. Chronic kidney disease and rapid decline in estimated glomerular filtration rate are associated with increased mortality in SCD patients.

NATURE REVIEWS NEPHROLOGY (2022)

Article Hematology

Frequency, pattern, and associations of renal iron accumulation in sickle/β-thalassemia patients

Antonella Meloni et al.

Summary: Renal iron accumulation is not common in sickle/beta-thalassemia patients, with a significantly lower frequency compared to homozygous SCD patients. Kidney T2* values are similar between sickle/beta-thalassemia and TM patients, but significantly lower in regularly transfused homozygous SCD patients. Age, gender, splenectomy, and transfusion or chelation therapy are not associated with global renal T2* values, but there is a significant inverse correlation with serum lactate dehydrogenase and indirect bilirubin.

ANNALS OF HEMATOLOGY (2022)

Article Hematology

Sickle Cell Nephropathy in the Pediatric Population

Kabir O. Olaniran et al.

BLOOD PURIFICATION (2019)

Review Hematology

Beta-thalassemia: renal complications and mechanisms: a narrative review

Christos Demosthenous et al.

HEMATOLOGY (2019)

Article Health Care Sciences & Services

GRADE Evidence to Decision (EtD) frameworks for adoption, adaptation, and de novo development of trustworthy recommendations: GRADE-ADOLOPMENT

Holger J. Schunemann et al.

JOURNAL OF CLINICAL EPIDEMIOLOGY (2017)

Article Hematology

Factors associated with survival in a contemporary adult sickle cell disease cohort

Hany Elmariah et al.

AMERICAN JOURNAL OF HEMATOLOGY (2014)

Review Hematology

How I treat renal complications in sickle cell disease

Claire C. Sharpe et al.

Review Urology & Nephrology

Deferasirox nephrotoxicity-the knowns and unknowns

Juan Daniel Diaz-Garcia et al.

NATURE REVIEWS NEPHROLOGY (2014)

Article Public, Environmental & Occupational Health

Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000

Frederic B. Piel et al.

LANCET GLOBAL HEALTH (2014)

Article Urology & Nephrology

Mechanisms of Renal Disease in β-Thalassemia

Khaled M. Musallam et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2012)

Review Hematology

Renal complications in transfusion-dependent beta thalassaemia

Claudio Ponticelli et al.

BLOOD REVIEWS (2010)

Article Urology & Nephrology

Fanconi Syndrome Due to Deferasirox

Cedric Rafat et al.

AMERICAN JOURNAL OF KIDNEY DISEASES (2009)

Article Public, Environmental & Occupational Health

Global epidemiology of haemoglobin disorders and derived service indicators

Bernadette Modell et al.

BULLETIN OF THE WORLD HEALTH ORGANIZATION (2008)

Review Urology & Nephrology

Chronic hypoxia and tubulointerstitial injury: A final common pathway to end-stage renal failure

Masaomi Nangaku

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2006)