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1.
Qatar Medical Journal. 2006; 15 (1): 21-24
in English | IMEMR | ID: emr-80405

ABSTRACT

Acute pancreatitis has a variety of presentations from self-limiting abdominal pain to development of local and systemic complications resulting in sepsis, multi-organ dysfunction, extended intensive care stay and death. Very good quality of life in survivors justifies an optimal therapy in an intensive care setup. The records of 91 patients with acute pancreatitis were reviewed retrospectively. There was a significant difference [p<0.001] between those with edematous pancreatitis and those with necrotic pancreatitis as regards the length of ICU stay and severity scores: Ranson and SOFA [Sepsis-related Organ Failure Assessment]. The most common cause of pancreatitis was biliary [70.3 percent] followed by hyperlipidemia [12.1 percent], post ERCP [5.5 percent], trauma [4.4 percent], idiopathic [6.6 percent] and in one case, ascariasis. Common associated diseases were hypertension [33 percent] and diabetes mellitus [25.3 percent]. Six patients with necrotic pancreatitis died. It is concluded that acute pancreatitis treated in an intensive care unit has a favorable outcome and that a combination of Ranson and SOFA scores with CT index helps in establishing the prognosis


Subject(s)
Humans , Male , Female , Pancreatitis/etiology , Pancreatitis, Acute Necrotizing , Acute Disease , Intensive Care Units , Retrospective Studies , Multiple Organ Failure , Cholangiopancreatography, Endoscopic Retrograde
2.
Qatar Medical Journal. 2005; 14 (2): 54-56
in English | IMEMR | ID: emr-177806

ABSTRACT

Hemolytic uraemic syndrome [HUS] and thrombotic thrombocytopenic purpura [TTP] are described as acute syndromes with multisystem abnormalities and pentad of thrombocytopenia, microangiopathic hemolysis, neurological symptoms, renal impairment and fever. Both diseases were believed to form a continuum of the same disease, but recently it was found, that they were having a different pathophysiology, as TTP patients have a deficiency in von wilbrand factor [vWF] cleavage protease. When renal involvement is severe with little or no neurological manifestation, this microangiopathy is termed as haemolytic-uraemic syndrome. If the hemolytic uraemic syndrome is not associated with diarrhoea, it is called D-negative or atypical HUS. This subdivision is ofetiological and prognostic importance. TTP-HUS is associated with high maternal and fetal morbidity and mortality. Treatment of these syndromes differs from syndrome of hemolysis with elevated liver enzymes [HELLP syndrome] and acute fatty liver of pregnancy hence accurate diagnosis is important for optimal therapy. Plasma transfusion and plasmapheresis have revolutionized management of TTP and HUS by increasing survival 80% to 90%. Here we are reporting a case of D-negative hemolytic uraemic syndrome associated with pregnancy causing in-trauterine fetal death. Diagnosis made on clinical and he-matological findings, successfully treated by plasmapheresis with residual maternal renal impairment. We are presenting this case, as it is rare disorder associated with high mortality and morbidity, to increase awareness about disease, its diagnosis and management

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