Andere Kunden interessierten sich auch für
![In Vitro and In Vivo Hemolysis]( "In Vitro and In Vivo Hemolysis")
In Vitro and In Vivo Hemolysis26,99 €![Gastrointestinal Endoscopy in the Cancer Patient]( "Gastrointestinal Endoscopy in the Cancer Patient")
Gastrointestinal Endoscopy in the Cancer Patient208,99 €![Diagnose]( "Diagnose")
Diagnose109,95 €![Geriatrische Gastroenterologie]( "Geriatrische Gastroenterologie")
Geriatrische Gastroenterologie92,95 €![Evidence-based Gastroenterology and Hepatology 4e]( "Evidence-based Gastroenterology and Hepatology 4e")
Evidence-based Gastroenterology and Hepatology 4e321,99 €![Colonoscopy]( "Colonoscopy")
Colonoscopy516,99 €![Problem-Based Approach to Gastroenterology and Hepatology]( "Problem-Based Approach to Gastroenterology and Hepatology")
Problem-Based Approach to Gastroenterology and Hepatology88,99 €
This book presents the long-awaited critical edition of an unpublished manuscript of 277 pages containing Twardowski’s lecture notes on logic given in German at the University of Vienna. As to length, language and topic, this text is unique among the works of the author, who is renowned for his Zur Lehre vom Inhalt und Gegenstand der Vorstellungen (1894), an influential but short book that has been out of stock for a long time already. In Logik Twardowski’s ideas are exposed in a much more extensive and interestingly revised form. The rest of Twardowski’s production is in Polish, a language inaccessible to many readers.
This edition will be of special interest to philosophers interested in the scientific philosophy in Vienna before the Wiener Kreis, to phenomenologists and anyone interested in early phenomenology and Husserl’s thought, to historians of early analytic philosophy, and particularly to specialists of Austrian philosophy and the continental analytic tradition from Bolzano to Tarski, for whom the book will be a truly indispensable source.
Peritoneal dissemination is a common route of cancer metastasis. The benefit of administering chemotherapy directly into the peritoneal cavity is supported by preclinical and pharmacokinetic data. In comparison to intravenous (IV) treatment, intraperitoneal (IP) administration results in a several-fold increase in drug concentration within the abdominal cavity. There is now growing evidence from clinical studies showing a survival advantage for IP chemotherapy in various tumor typies, including ovarian, gastric and colorectal cancer.
However, while the use of IP chemotherapy is slowly gaining acceptance, it is not universal, largely due to the greater toxicity associated with this approach. Moreover, efficacy of IP chemotherapy is limited by poor distribution within the abdominal cavity and by poor tissue penetration.
A new way of IP chemotherapy is the application of cytotoxics in form of a pressurized aerosol into the abdominal of thoracic cavity. Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is applied through laparoscopic access using two balloon trocars in an operating room equipped with laminar air-flow. In a first step,a normothermic capnoperitoneum is established with a pressure of 12 mmHg. A cytotoxic solution (about 10% of a normal systemic dose) is nebulized with a micropump into the abdominal cavity, and maintained for 30 min. The aerosol is then removed through a closed suction system.
Applying an aerosol in the peritoneal cavity allows a homogeneous distribution of the chemotherapeutic agent within the abdomen. Furthermore, an artificial pressure gradient is generated that overcomes tumoral interstitial fluid pressure, an obstacle in cancer therapy. This results in a higher local drug concentration compared to conventional IP or IV chemotherapy. At the same time the plasma concentration of the chemotherapeutic agent remains low.
In first clinical studies with limited number of patients in ovarian, gastric and colorectal cancer, as well as peritoneal mesothelioma, PIPAC has obtained encouraging tumor response rates and survival, with a low-side effects profile. Larger clinical trials are currently ongoing to examine if these data can be reproduced and extrapolated to other situations.
This edition will be of special interest to philosophers interested in the scientific philosophy in Vienna before the Wiener Kreis, to phenomenologists and anyone interested in early phenomenology and Husserl’s thought, to historians of early analytic philosophy, and particularly to specialists of Austrian philosophy and the continental analytic tradition from Bolzano to Tarski, for whom the book will be a truly indispensable source.
Peritoneal dissemination is a common route of cancer metastasis. The benefit of administering chemotherapy directly into the peritoneal cavity is supported by preclinical and pharmacokinetic data. In comparison to intravenous (IV) treatment, intraperitoneal (IP) administration results in a several-fold increase in drug concentration within the abdominal cavity. There is now growing evidence from clinical studies showing a survival advantage for IP chemotherapy in various tumor typies, including ovarian, gastric and colorectal cancer.
However, while the use of IP chemotherapy is slowly gaining acceptance, it is not universal, largely due to the greater toxicity associated with this approach. Moreover, efficacy of IP chemotherapy is limited by poor distribution within the abdominal cavity and by poor tissue penetration.
A new way of IP chemotherapy is the application of cytotoxics in form of a pressurized aerosol into the abdominal of thoracic cavity. Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is applied through laparoscopic access using two balloon trocars in an operating room equipped with laminar air-flow. In a first step,a normothermic capnoperitoneum is established with a pressure of 12 mmHg. A cytotoxic solution (about 10% of a normal systemic dose) is nebulized with a micropump into the abdominal cavity, and maintained for 30 min. The aerosol is then removed through a closed suction system.
Applying an aerosol in the peritoneal cavity allows a homogeneous distribution of the chemotherapeutic agent within the abdomen. Furthermore, an artificial pressure gradient is generated that overcomes tumoral interstitial fluid pressure, an obstacle in cancer therapy. This results in a higher local drug concentration compared to conventional IP or IV chemotherapy. At the same time the plasma concentration of the chemotherapeutic agent remains low.
In first clinical studies with limited number of patients in ovarian, gastric and colorectal cancer, as well as peritoneal mesothelioma, PIPAC has obtained encouraging tumor response rates and survival, with a low-side effects profile. Larger clinical trials are currently ongoing to examine if these data can be reproduced and extrapolated to other situations.