Literature DB >> 15857006

Multiorgan dysfunction syndrome in sickle cell disease.

Sujata Hiran1.   

Abstract

OBJECTIVE: Concurrent failure of multiple organs in patients of sickle cell disease (SCD) has rarely been reported. The main objective of this study was to highlight the multiorgan dysfunction (MODS) that occurs in some patients during sickle cell crisis.
METHODS: Ten episodes of multiorgan failure were identified with sickle cell disease and defining criteria of organ failure of two or more organs that is lung, liver, or renal were established according to Acute Physiological and Chronic Health Evaluation - II (APACHE-II) criteria.
RESULTS: Most episodes occurred during vaso-occlusive crisis, which was associated with a severe pain event. The onset of organ failure was associated with fever, rapid fall in haematocrit, platelet count and altered sensorium, later organ failure set in. Respiratory, hepatic, and kidney failure (all the three organs) were present in three of the ten patients who were in sickle crisis. Of this we lost one patient despite exchange transfusion and ventilator support. Of the four patients who had respiratory failure accompanied by hepatic failure, one patient died due to associated septicemia. Respiratory failure with renal involvement was seen in two patients whereas hepatic and renal failure was present in only one patient. Except for two, all other patients improved after aggressive blood transfusions.
CONCLUSION: Acute multiorgan failure is a life threatening complication of SCD, which can exhibit without any evidence of chronic organ damage and is easily reversed by prompt and aggressive transfusion therapy.

Entities:  

Mesh:

Year:  2005        PMID: 15857006

Source DB:  PubMed          Journal:  J Assoc Physicians India        ISSN: 0004-5772


  4 in total

1.  Oxidative stress and associated clinical manifestations in malaria and sickle cell (HbSS) comorbidity.

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Journal:  PLoS One       Date:  2022-06-08       Impact factor: 3.752

Review 2.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

3.  Fat Embolism Syndrome in Sickle Cell β-Thalassemia Patient With Osteonecrosis: An Uncommon Presentation in a Young Adult.

Authors:  Vikram Sangani; Mytri Pokal; Mamtha Balla; Ganesh Prasad Merugu; Waleed Khokher; Vijay Gayam; Venu Madhav Konala
Journal:  J Investig Med High Impact Case Rep       Date:  2021 Jan-Dec

Review 4.  Prodrugs for the treatment of neglected diseases.

Authors:  Man Chin Chung; Elizabeth Igne Ferreira; Jean Leandro Santos; Jeanine Giarolla; Daniela Gonçales Rando; Adélia Emília Almeida; Priscila Longhin Bosquesi; Renato Farina Menegon; Lorena Blau
Journal:  Molecules       Date:  2007-03-19       Impact factor: 4.411

  4 in total

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