Zusammenfassung
Bei einer Inzidenz von jährlich 30–45 pro 100.000 Einwohner ist die akute Pankreatitis (AP) in Deutschland in mehr als zwei Drittel der Fälle biliärer oder alkoholischer Genese. Daneben kann die AP iatrogen, metabolisch, genetisch oder durch einen Tumor verursacht sein. Die Diagnose stützt sich auf das Vorhandensein des typischen epigastrischen Schmerzes mit Ausstrahlung in den Rücken und die mindestens 3‑fache Erhöhung von Lipase oder Amylase im Serum. Bei schmalem „therapeutischem Fenster“ ist die frühzeitige Risikobewertung essenziell, um bei schwerer AP (Mortalität bis 42 %) rechtzeitig intensiv überwachen und therapieren zu können. Ungünstige Prognosefaktoren sind Erhöhung von Harnstoff, Hämatokrit und Blutzucker im Serum. Daneben werden verschiedene Scores eingesetzt. Zur Schweregradeinteilung im Verlauf wird die Atlanta-Klassifikation herangezogen. Die Entfernung eines impaktierten Gallensteins bei biliärer AP mittels endoskopischer retrograder Cholangiographie (ERC) ist die einzige kausale Therapie. Die ERC ist auch bei Zeichen der Cholangitis sowie bei schwerer biliärer AP indiziert. Schmerztherapie und Flüssigkeitssubstitution sind die wichtigsten symptomatischen Maßnahmen. Um extravasale Flüssigkeitsverluste auszugleichen, sollte in der Frühphase der AP eine Volumenzufuhr mit Kristalloiden erfolgen. Im Intensivsetting steht neben der Echokardiographie ein erweitertes hämodynamisches Monitoring zur zielgerichteten Volumentherapie zur Verfügung. Eine antibiotische Prophylaxe ist bei schwerer AP möglicherweise vorteilhaft. Die Ernährung sollte möglichst frühzeitig enteral erfolgen. Eine chirurgische Intervention ist Komplikationen (Blutung, abdominelles Kompartmentsyndrom) und anderweitig nicht erreichbaren infizierten Nekrosen vorbehalten.
Abstract
In Germany, acute pancreatitis (AP) has an incidence of 30–45 cases per 100,000 person–years. More than two of three cases are caused by gallstones or alcohol. Iatrogenic, metabolic or malignant etiologies are markedly less frequent. Diagnosis is established based on the typical epigastric pain radiating to the back and a three-fold increase in serum lipase or amylase. Early prognosis is crucial to optimize therapy in patients with severe AP with a mortality of up to 42%. Elevation of blood urea nitrogen, hematocrit or blood glucose are early predictors of poor outcome. Furthermore, various scores can be used for risk assessment. Finally, the Atlanta classification can be used to classify the long-term severity of AP. Endoscopic retrograde cholangiography (ERC) with removal of the incarcerated gallstone should be performed in case of cholangitis and/or severe biliary AP. ERC is the only causal therapy in AP. Pain management and fluid resuscitation are the most important symptomatic measures. Early goal-directed fluid resuscitation using colloids might mitigate severe courses of AP. In the critical care setting, therapy should be guided by echocardiography and advanced hemodynamic monitoring. Antibiotic prophylaxis is likely advantageous in patients with severe AP. Furthermore, enteral nutrition should be provided as early as feasible. If these approaches are not possible or in case of complications (e.g., intra-abdominal compartment syndrome or bleeding), surgery is recommended (“step-up” approach).
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W. Huber, J. Schneider und R.M. Schmid geben an, dass kein Interessenkonflikt besteht.
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A. Koch, Aachen
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Huber, W., Schneider, J. & Schmid, R.M. Therapie der schweren akuten Pankreatitis. Gastroenterologe 15, 41–52 (2020). https://doi.org/10.1007/s11377-020-00422-1
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DOI: https://doi.org/10.1007/s11377-020-00422-1