Usefulness of a nonmachinery based system for the reinfusion of cell-free and concentrated autogenous ascitic fluid. 1997

S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
Department of Internal Medicine, Murakami Memorial Hospital, Asahi University, Gifu, Japan.

A nonmachinery based system using gravity dependent flow for the treatment and reinfusion of ascitic fluid was developed, and its usefulness was assessed. In a preliminary study using bovine plasma, samples with protein concentrations below 5.0 g/dl were found to be treatable with this system. Bovine plasma containing blood, prepared to 0.5% hematocrit and with a protein concentration of 3.0 g/dl, was also treatable. We conducted a clinical study of 1,799 treatment sessions (1,495 using a machinery based system and 304 using a nonmachinery based system) of 343 patients with ascites refractory to various treatments. The recovery ratio of protein from the original ascitic fluid was 96% using the nonmachinery based system and 77% with the machinery based system (p < 0.01). Of 253 continuous reinfusions of ascitic fluid using the nonmachinery based system, the original ascitic fluid at protein concentrations below 2.5 g/dl was treatable. Original ascitic fluid below a hematocrit of 0.7% (protein concentration, 1.4 g/dl) was also treatable. This new procedure was simple and time and labor saving; the high recovery ratio of protein also demonstrated the usefulness of the new system.

UI MeSH Term Description Entries
D007263 Infusions, Parenteral The administration of liquid medication, nutrient, or other fluid through some other route than the alimentary canal, usually over minutes or hours, either by gravity flow or often by infusion pumping. Intra-Abdominal Infusions,Intraperitoneal Infusions,Parenteral Infusions,Peritoneal Infusions,Infusion, Intra-Abdominal,Infusion, Intraperitoneal,Infusion, Parenteral,Infusion, Peritoneal,Infusions, Intra-Abdominal,Infusions, Intraperitoneal,Infusions, Peritoneal,Intra Abdominal Infusions,Intra-Abdominal Infusion,Intraperitoneal Infusion,Parenteral Infusion,Peritoneal Infusion
D008103 Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. Cirrhosis, Liver,Fibrosis, Liver,Hepatic Cirrhosis,Liver Fibrosis,Cirrhosis, Hepatic
D008113 Liver Neoplasms Tumors or cancer of the LIVER. Cancer of Liver,Hepatic Cancer,Liver Cancer,Cancer of the Liver,Cancer, Hepatocellular,Hepatic Neoplasms,Hepatocellular Cancer,Neoplasms, Hepatic,Neoplasms, Liver,Cancer, Hepatic,Cancer, Liver,Cancers, Hepatic,Cancers, Hepatocellular,Cancers, Liver,Hepatic Cancers,Hepatic Neoplasm,Hepatocellular Cancers,Liver Cancers,Liver Neoplasm,Neoplasm, Hepatic,Neoplasm, Liver
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D010537 Peritoneum A membrane of squamous EPITHELIAL CELLS, the mesothelial cells, covered by apical MICROVILLI that allow rapid absorption of fluid and particles in the PERITONEAL CAVITY. The peritoneum is divided into parietal and visceral components. The parietal peritoneum covers the inside of the ABDOMINAL WALL. The visceral peritoneum covers the intraperitoneal organs. The double-layered peritoneum forms the MESENTERY that suspends these organs from the abdominal wall. Parietal Peritoneum,Peritoneum, Parietal,Peritoneum, Visceral,Visceral Peritoneum,Parametrium,Parametriums
D011108 Polymers Compounds formed by the joining of smaller, usually repeating, units linked by covalent bonds. These compounds often form large macromolecules (e.g., BIOPOLYMERS; PLASTICS). Polymer
D011506 Proteins Linear POLYPEPTIDES that are synthesized on RIBOSOMES and may be further modified, crosslinked, cleaved, or assembled into complex proteins with several subunits. The specific sequence of AMINO ACIDS determines the shape the polypeptide will take, during PROTEIN FOLDING, and the function of the protein. Gene Products, Protein,Gene Proteins,Protein,Protein Gene Products,Proteins, Gene
D005260 Female Females
D005374 Filtration A process of separating particulate matter from a fluid, such as air or a liquid, by passing the fluid carrier through a medium that will not pass the particulates. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Filtrations

Related Publications

S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
January 1993, [Rinsho ketsueki] The Japanese journal of clinical hematology,
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
March 1992, Internal medicine (Tokyo, Japan),
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
January 1977, Transactions - American Society for Artificial Internal Organs,
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
March 1997, American journal of kidney diseases : the official journal of the National Kidney Foundation,
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
February 1979, Revista clinica espanola,
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
September 1983, Nihon Sanka Fujinka Gakkai zasshi,
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
May 1993, Digestive diseases and sciences,
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
August 1997, Digestive diseases and sciences,
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
March 1983, Casopis lekaru ceskych,
S Katoh, and T Kojima, and K Itoh, and S Yoneyama, and K Ida, and S Nakaji
January 1991, Japanese journal of medicine,
Copied contents to your clipboard!