Effect of ranitidine on gastric intramucosal pH in critically ill patients. 1998

X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
Department of Internal Medicine, Hospital de Sabadell, Barcelona, Spain. xcalvet@siberia.chpt.es

OBJECTIVE To determine whether ranitidine a) increases the values of gastric intramucosal pH (pHi) in critically ill patients, as determined by tonometry; b) reduces the variability of these measurements. METHODS Prospective, double blind, randomized, placebo-controlled study. METHODS General Intensive Care Unit of a teaching hospital. METHODS Twenty-five critically ill, mechanically ventilated patients requiring arterial catheter and nasogastric tube. METHODS Tonometer placement; blind, random administration of intravenous ranitidine (50 mg) or placebo. RESULTS Tonometer saline PCO2 (PCO2i), arterial blood gases, gastric juice pH and pHi were determined immediately before, and 2, 4, 6 and 8 h after, ranitidine (12 patients) or placebo (13 patients). Ranitidine significantly increased gastric juice pH, but did not affect PCO2i or pHi; pHi was 7.34 +/- 0.14 before ranitidine, and 7.30 +/- 0.12, 7.31 +/- 0.11, 7.31 +/- 0.14 and 7.31 +/- 0.12-2, 4, 6 and 8 h, respectively, after ranitidine administration (p = 0.55). Ranitidine did not modify the coefficients of variation of PCO2i or pHi, either. No significant changes in gastric juice pH, PCO2i or pHi were observed in the placebo group. CONCLUSIONS In critically ill patients, ranitidine has no effect on pHi values, and does not increase the reproducibility of pHi measurements.

UI MeSH Term Description Entries
D007362 Intensive Care Units Hospital units providing continuous surveillance and care to acutely ill patients. ICU Intensive Care Units,Intensive Care Unit,Unit, Intensive Care
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D011446 Prospective Studies Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group. Prospective Study,Studies, Prospective,Study, Prospective
D011899 Ranitidine A non-imidazole blocker of those histamine receptors that mediate gastric secretion (H2 receptors). It is used to treat gastrointestinal ulcers. AH-19065,Biotidin,N (2-(((5-((Dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine,Ranisen,Ranitidin,Ranitidine Hydrochloride,Sostril,Zantac,Zantic,AH 19065,AH19065,Hydrochloride, Ranitidine
D012121 Respiration, Artificial Any method of artificial breathing that employs mechanical or non-mechanical means to force the air into and out of the lungs. Artificial respiration or ventilation is used in individuals who have stopped breathing or have RESPIRATORY INSUFFICIENCY to increase their intake of oxygen (O2) and excretion of carbon dioxide (CO2). Ventilation, Mechanical,Mechanical Ventilation,Artificial Respiration,Artificial Respirations,Mechanical Ventilations,Respirations, Artificial,Ventilations, Mechanical
D004311 Double-Blind Method A method of studying a drug or procedure in which both the subjects and investigators are kept unaware of who is actually getting which specific treatment. Double-Masked Study,Double-Blind Study,Double-Masked Method,Double Blind Method,Double Blind Study,Double Masked Method,Double Masked Study,Double-Blind Methods,Double-Blind Studies,Double-Masked Methods,Double-Masked Studies,Method, Double-Blind,Method, Double-Masked,Methods, Double-Blind,Methods, Double-Masked,Studies, Double-Blind,Studies, Double-Masked,Study, Double-Blind,Study, Double-Masked
D005260 Female Females
D005753 Gastric Mucosa Lining of the STOMACH, consisting of an inner EPITHELIUM, a middle LAMINA PROPRIA, and an outer MUSCULARIS MUCOSAE. The surface cells produce MUCUS that protects the stomach from attack by digestive acid and enzymes. When the epithelium invaginates into the LAMINA PROPRIA at various region of the stomach (CARDIA; GASTRIC FUNDUS; and PYLORUS), different tubular gastric glands are formed. These glands consist of cells that secrete mucus, enzymes, HYDROCHLORIC ACID, or hormones. Cardiac Glands,Gastric Glands,Pyloric Glands,Cardiac Gland,Gastric Gland,Gastric Mucosas,Gland, Cardiac,Gland, Gastric,Gland, Pyloric,Glands, Cardiac,Glands, Gastric,Glands, Pyloric,Mucosa, Gastric,Mucosas, Gastric,Pyloric Gland
D006635 Histamine H2 Antagonists Drugs that selectively bind to but do not activate histamine H2 receptors, thereby blocking the actions of histamine. Their clinically most important action is the inhibition of acid secretion in the treatment of gastrointestinal ulcers. Smooth muscle may also be affected. Some drugs in this class have strong effects in the central nervous system, but these actions are not well understood. Antihistaminics, H2,H2 Receptor Blockader,Histamine H2 Antagonist,Histamine H2 Blocker,Histamine H2 Receptor Antagonist,Histamine H2 Receptor Antagonists,Histamine H2 Receptor Blockader,Histamine H2 Receptor Blockaders,Antagonists, Histamine H2,Blockaders, Histamine H2 Receptor,H2 Receptor Blockaders,Histamine H2 Blockers,Receptor Antagonists, Histamine H2,Receptor Blockaders, H2,Antagonist, Histamine H2,Blockader, H2 Receptor,Blockaders, H2 Receptor,Blocker, Histamine H2,Blockers, Histamine H2,H2 Antagonist, Histamine,H2 Antagonists, Histamine,H2 Antihistaminics,H2 Blocker, Histamine,H2 Blockers, Histamine,Receptor Blockader, H2

Related Publications

X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
February 1992, Lancet (London, England),
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
January 2001, Critical care medicine,
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
January 2019, The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG,
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
June 1998, Critical care medicine,
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
January 2000, Critical care medicine,
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
August 1998, Critical care medicine,
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
January 1997, Intensive care medicine,
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
April 1996, Intensive care medicine,
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
January 1992, Lancet (London, England),
X Calvet, and F Baigorri, and M Duarte, and P Saura, and C Royo, and D Joseph, and A Mas, and A Artigas
January 2008, Clinical drug investigation,
Copied contents to your clipboard!