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2.
Aliment Pharmacol Ther ; 16(5): 899-907, 2002 May.
Article in English | MEDLINE | ID: mdl-11966498

ABSTRACT

BACKGROUND: The use of over-the-counter antacids has increased in children under the age of 12 years, and has been followed by an apparent increase in the use of over-the-counter histamine-2 receptor antagonists. However, the pharmacokinetic and pharmacodynamic effects of over-the-counter histamine-2 receptor antagonists in the paediatric population are largely unknown. AIM: To evaluate the pharmacokinetics and pharmacodynamics of a single dose of the over-the-counter histamine-2 receptor antagonist, ranitidine, 75 mg, in children with symptoms of gastro-oesophageal reflux disease. METHODS: Children aged between 4 and 11 years with symptoms of heartburn suspected to be due to gastro-oesophageal reflux disease were recruited at six clinical centres. Following a single dose of either oral ranitidine, 75 mg (n=19), or placebo (n=10), recording of intragastric pH and serial blood sampling were carried out for 6 h. RESULTS: The estimated pharmacokinetic parameters of ranitidine, 75 mg, were as follows: the median Cmax value of 477 ng/mL occurred within a median of 2.5 h after dosing, and the median half-life was 2.0 h. The intragastric pH began to rise approximately 30 min after dosing with ranitidine to a peak of pH; 4. The pH in the ranitidine group remained higher than that in the placebo group throughout the 6-h evaluation period. Adverse events were generally mild. CONCLUSIONS: Ranitidine, 75 mg, significantly increased the intragastric pH in children aged 4-11 years. The pharmacokinetic and pharmacodynamic profiles were similar to those in adults. Ranitidine, 75 mg, appears to be effective for the control of intragastric acidity for 5-6 h in children aged 4-11 years.


Subject(s)
Anti-Ulcer Agents , Gastroesophageal Reflux/drug therapy , Ranitidine , Anti-Ulcer Agents/pharmacokinetics , Anti-Ulcer Agents/pharmacology , Anti-Ulcer Agents/therapeutic use , Area Under Curve , Child , Child, Preschool , Double-Blind Method , Female , Half-Life , Humans , Hydrogen-Ion Concentration , Male , Ranitidine/pharmacokinetics , Ranitidine/pharmacology , Ranitidine/therapeutic use
3.
Am J Physiol Endocrinol Metab ; 278(5): E877-84, 2000 May.
Article in English | MEDLINE | ID: mdl-10780944

ABSTRACT

The threonine dehydrogenase (TDG) pathway is a significant route of threonine degradation, yielding glycine in experimental animals, but has not been accurately quantitated in humans. Therefore, the effect of a large excess of dietary threonine, given either as free amino acid (+Thr) or as a constituent of protein (+P-Thr), on threonine catabolism to CO(2) and to glycine was studied in six healthy adult males using a 4-h constant infusion of L-[1-(13)C]threonine and [(15)N]glycine. Gas chromatography-combustion isotope ratio mass spectrometry was used to determine [(13)C]glycine produced from labeled threonine. Threonine intakes were higher on +Thr and +P-Thr diets compared with control (126, 126, and 50 micromol x kg(-1) x h(-1), SD 8, P < 0.0001). Threonine oxidation to CO(2) increased threefold in subjects on +Thr and +P-Thr vs. control (49, 45, and 15 micromol x kg(-1) x h(-1), SD 6, P < 0.0001). Threonine conversion to glycine tended to be higher on +Thr and +P-Thr vs. control (3.5, 3.4, and 1.6 micromol x kg(-1) x h(-1), SD 1.3, P = 0.06). The TDG pathway accounted for only 7-11% of total threonine catabolism and therefore is a minor pathway in the human adult.


Subject(s)
Alcohol Oxidoreductases/metabolism , Threonine/blood , Adult , Aminobutyrates/blood , Carbon Isotopes , Dietary Proteins/administration & dosage , Energy Metabolism , Gas Chromatography-Mass Spectrometry , Glycine/administration & dosage , Glycine/blood , Humans , Male , Nitrogen Isotopes , Oxidation-Reduction , Threonine/administration & dosage
4.
J Zoo Wildl Med ; 30(2): 268-72, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10484144

ABSTRACT

A 6-mo-old hand-raised male western lowland gorilla (Gorilla gorilla gorilla) was diagnosed with acute lymphocytic leukemia based on complete blood count and bone marrow cytology. Clinical signs of the disease were pyrexia, abdominal distention, splenomegaly, and lethargy. Acute lymphocytic leukemia has rarely been reported in this species, and therapy was based on human oncologic protocols. Remission induction chemotherapy resulted in complete clearing of leukemia cells from the bone marrow. Consolidation and maintenance chemotherapy followed. Therapy was facilitated by the use of an infusion port for i.v. treatments and an indwelling lumbar catheter for intrathecal therapy. Side effects associated with chemotherapy were inappetence, moderate alopecia, pancytopenia resulting in sepsis, and bleeding tendency. In spite of initial success, the leukemia reappeared 120 days into treatment. The gorilla was euthanized 7 days later when respiratory distress developed. Intensive care by the animal staff was a key factor in the treatment of this gorilla.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Ape Diseases/drug therapy , Gorilla gorilla , Precursor Cell Lymphoblastic Leukemia-Lymphoma/veterinary , Animals , Ape Diseases/diagnosis , Bone Marrow Cells/pathology , Euthanasia/veterinary , Karyotyping/veterinary , Liver/pathology , Male , Precursor Cell Lymphoblastic Leukemia-Lymphoma/diagnosis , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Recurrence , Remission Induction , Spleen/pathology
5.
Gastrointest Endosc ; 44(3): 235-8, 1996 Sep.
Article in English | MEDLINE | ID: mdl-8885339

ABSTRACT

BACKGROUND: Percutaneous endoscopic gastrostomy (PEG) tubes are often removed by cutting the tubing at skin level and allowing the internal components to pass through the gastrointestinal tract. This technique is commonly used in adults, but little information is available concerning its safety in younger patients. METHODS: To assess the safety of this approach in children, the clinical courses of all patients who had undergone PEG tube removal in our pediatric gastroenterology unit over a 3-year period were reviewed. RESULTS: Five of 11 patients in whom the internal components were allowed to pass developed significant complications. Three required subsequent endoscopic removal of the internal component due to persistent vomiting, one died from complications of esophageal perforation caused by the retained internal component, and one developed a gastrocutaneous fistula containing the retained bumper 2 years after PEG tube removal. Significant complications occurred more often in the younger and smaller patients. CONCLUSIONS: Small children are at greater risk than adults for developing serious complications associated with unremoved PEG tube internal components. If passage of the internal components cannot be confirmed after 2 weeks, chest and abdominal radiographs should be obtained.


Subject(s)
Gastrostomy/instrumentation , Adolescent , Adult , Child , Child, Preschool , Endoscopy , Esophageal Perforation/etiology , Female , Gastrostomy/adverse effects , Gastrostomy/mortality , Humans , Infant , Male , Postoperative Complications/mortality , Safety
6.
J Okla State Med Assoc ; 89(7): 233-7, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8783522

ABSTRACT

OBJECTIVE: To study the hypothesis that environmental tobacco smoke exposure in infants diagnosed with an apparent life-threatening event (ALTE) could be a contributing factor to gastroesophageal reflux. METHODS: Thirty-four polygraphic recordings of combined esophageal pH study and respiration in infants with ALTE, age 4.1 +/- 4.9 months, range 0.4-27 months, were studied. This group of children had uncomplicated perinatal history, no congenital anomalies, no neuropathology, and no drug exposure. A written questionnaire was administered to the parents to determine the following: environmental variables, degree of environmental tobacco smoke (ETS) exposure (number of cigarettes/day), and nutrition (breast vs. bottle feeding). RESULTS: There was a strong correlation between pH study parameters and ETS exposure (p < 0.005). The esophageal pH parameters were markedly elevated in the ETS-exposed group and in this group there was a linear relation between the number of cigarettes smoked per day and reflux index, as well as reflux > 5 min/hr (p < 0.05, r = 0.46). Nursing mothers were less likely to be smokers (18.2% vs. 34.0%). The only significant respiratory finding was in the obstructive/mixed apnea group; there was strong association between ETS exposure and high reflux index (p < 0.05). CONCLUSION: We conclude that ETS exposure represents a significant contributing factor to GER. Pediatricians should systematically ask questions about the infant environment, explain the risk of ETS exposure to the caretaker, and recommend that children should remain in a smoke-free environment.


Subject(s)
Apnea/etiology , Gastroesophageal Reflux/etiology , Tobacco Smoke Pollution/adverse effects , Apnea/diagnosis , Apnea/epidemiology , Esophagus/metabolism , Female , Gastroesophageal Reflux/diagnosis , Humans , Hydrogen-Ion Concentration , Infant , Male , Monitoring, Physiologic , Retrospective Studies
8.
Semin Pediatr Surg ; 4(3): 147-51, 1995 Aug.
Article in English | MEDLINE | ID: mdl-7582884

ABSTRACT

Emesis is a common symptom resulting from adverse food reactions in infants. In this article the terms food allergy and food intolerance are defined and differentiated. The immunopathophysiology of food allergies is discussed along with useful diagnostic tests. Adverse reactions to common infant nutrients such as cow's milk and soy milk are described, and therapeutic use of "hypoallergenic" formulas is outlined.


Subject(s)
Food Hypersensitivity/complications , Vomiting/etiology , Celiac Disease/complications , Celiac Disease/diagnosis , Diagnosis, Differential , Food Hypersensitivity/diagnosis , Humans , Infant , Infant Food/adverse effects , Infant, Newborn , Milk Hypersensitivity/complications , Milk Hypersensitivity/diagnosis , Plant Proteins, Dietary/administration & dosage , Plant Proteins, Dietary/adverse effects , Soybean Proteins
9.
J Pediatr ; 122(2): 243-6, 1993 Feb.
Article in English | MEDLINE | ID: mdl-8429439

ABSTRACT

Energy expenditure during various activities of daily living in normally nourished female adolescents with cystic fibrosis was compared with that in matched healthy control subjects. Energy expenditure at rest, during sitting and standing, and during two levels of exercise was increased significantly in patients with cystic fibrosis (122% +/- 14%) compared with control subjects (104% +/- 10%) (p < 0.05), but incremental increases from one level of activity to another did not differ. We conclude that the various activities of daily living are not responsible for increased energy needs in female adolescents with cystic fibrosis.


Subject(s)
Activities of Daily Living , Cystic Fibrosis/metabolism , Energy Metabolism , Adolescent , Body Mass Index , Body Weight , Calorimetry , Case-Control Studies , Female , Humans , Nutrition Assessment , Physical Exertion , Rest
10.
JPEN J Parenter Enteral Nutr ; 13(1): 23-5, 1989.
Article in English | MEDLINE | ID: mdl-2494364

ABSTRACT

Two related studies were done to determine the incidence of bacterial contamination in enteral delivery systems that were used for 15 and 7.5 hr, rinsed after each use, and reused daily in vitro for 7 and 5 days, respectively. In the first study, systems infusing either a premixed formula (Ensure) or a hand-mixed formula (Vivonex) did not show bacterial growth until the 4th day, 1.0-2.0 X 10 colony-forming units per milliliter (CFU/ml) of Staphylococcus epidermidis. Thereafter there was sporadic growth of different organisms but never increasing growth during the 7 days of infusion. In the second study, systems with Ensure were initially contaminated with Staphylococcus aureus and Escherichia coli and reused for 5 days. S. aureus was eliminated by rinsing, but E. coli persisted in the delivery system at concentrations of 10(3)-10(6) CFU/ml. We conclude that clean enteral nutrition systems can be rinsed after short-infusion periods and reused up to 7 days in vitro without significant contamination; however, once a bag has become heavily contaminated some bacteria cannot be eradicated from the system by rinsing.


Subject(s)
Bacteria/isolation & purification , Enteral Nutrition/instrumentation , Equipment Contamination/prevention & control , Food, Formulated , Humans
11.
J Pediatr Surg ; 24(1): 42-4; Discussion 44-5, 1989 Jan.
Article in English | MEDLINE | ID: mdl-2723992

ABSTRACT

The frequency and clinical significance of gastroesophageal reflux (GER) in patients after percutaneous endoscopic gastrostomy (PEG) was determined. Ten children, aged 11 months to 15 years, who had normal preoperative extended esophageal pH monitoring were restudied after PEG. Of the ten patients, six developed GER with a pH score significantly higher than their initial one (40.5 +/- 3.3 pre-PEG v 129.5 +/- 24.2 post-PEG, P less than .005). Similarly, the mean post-PEG pH score was higher in patients with GER than in those without a change in score (129.5 +/- 24.2 v 33.8 +/- 2.8, P less than .005). None of these patients was symptomatic for GER immediately after the PEG, but within 10 months of surgery, three of six (50%) developed reflux-related symptoms. These data indicate that clinically significant GER is associated with PEG.


Subject(s)
Gastroesophageal Reflux/etiology , Gastrostomy/adverse effects , Adolescent , Child , Child, Preschool , Female , Gastroscopy , Humans , Infant , Male
12.
Arch Neurol ; 45(8): 903-5, 1988 Aug.
Article in English | MEDLINE | ID: mdl-2899428

ABSTRACT

We have identified ten children who developed gastritis after prolonged anticonvulsant therapy that included either valproic acid or divalproex sodium. Presenting symptoms were primarily feeding difficulties, including anorexia and refusal to eat. Vomiting was present in two thirds of the patients, with diarrhea, weight loss, and abdominal pain occurring less frequently. Occult blood in stool samples was a late development. All patients responded to therapy with H2-receptor antagonists, oral antacids, or both, with prolonged treatment often necessary to prevent relapse. Although gastrointestinal tract side effects are common with the initiation of valproate sodium therapy, feeding difficulties after long-term treatment are less common. Gastritis should be suspected in children receiving valproate therapy when feeding difficulties arise, particularly if the symptoms are persistent or recurrent.


Subject(s)
Gastritis/chemically induced , Valproic Acid/adverse effects , Adolescent , Antacids/therapeutic use , Anticonvulsants/therapeutic use , Child , Child, Preschool , Drug Therapy, Combination , Epilepsy/blood , Epilepsy/drug therapy , Female , Gastrins/blood , Gastritis/drug therapy , Histamine H2 Antagonists/therapeutic use , Humans , Male , Phenytoin/therapeutic use , Valproic Acid/therapeutic use
14.
J Pediatr Gastroenterol Nutr ; 7(3): 359-66, 1988.
Article in English | MEDLINE | ID: mdl-3385548

ABSTRACT

In order to compare three premedication regimens, 58 children and adolescents were randomized to three groups: Group I, meperidine intramuscular; Group II, atropine intramuscular and diazepam intravenous; and Group III, meperidine, promethazine, and chlorpromazine intramuscular. Almost all patients required supplemental intravenous diazepam or meperidine to obtain adequate sedation. An endoscopist without knowledge of the medication group scored each patient for adequacy of sedation. Sedation was more effective in Group III than in Groups I and II (p less than 0.005); however, Group III patients were less arousable at completion of the procedure (p less than 0.0005) and had a greater duration of sedation (220 min compared with 56 and 88 min for Groups I and II, respectively, p less than 0.001). Complications were minor and not associated with any specific treatment. The evidence from this study supports the following conclusions: (a) adequate sedation for esophagogastroduodenoscopy in pediatric patients requires sedation with more than one of the drugs used in this study; and (b) the regimen meperidine, promethazine, and chlorpromazine, with diazepam supplement, was superior in providing sedation, but patients required a longer period of recovery than did patients sedated with one of the other regimens.


Subject(s)
Duodenoscopy , Esophagoscopy , Gastroscopy , Premedication , Adolescent , Adult , Atropine/administration & dosage , Child , Child, Preschool , Chlorpromazine/administration & dosage , Diazepam/administration & dosage , Double-Blind Method , Duodenoscopy/adverse effects , Esophagoscopy/adverse effects , Female , Gastroscopy/adverse effects , Humans , Infant , Injections, Intramuscular , Injections, Intravenous , Male , Meperidine/administration & dosage , Promethazine/administration & dosage , Random Allocation , Sleep Stages/drug effects
15.
J Pediatr Gastroenterol Nutr ; 7(1): 64-7, 1988.
Article in English | MEDLINE | ID: mdl-3335988

ABSTRACT

As an intravenous injection is not used in our premedication of infants and children for small bowel biopsy, we investigated what effects oral metoclopramide might have on small bowel biopsy procedure time and fluoroscopy time. Eighteen infants and children were randomized to receive 0.2 mg/kg metoclopramide or placebo orally, 40-45 min before starting the procedure, and the procedure was monitored for the time required for the biopsy capsule to reach the pylorus, to cross into the proximal duodenum, and to reach the biopsy site. Corresponding fluoroscopy times were recorded as well. Mean total procedure time was less for those treated with metoclopramide, 43.7 +/- 11 min, than for controls, 86.5 +/- 15.5 min (p less than 0.005). Mean total fluoroscopy time was also less in treated patients (40.9 +/- 11.5 s versus control 84.4 +/- 17 s) (p less than 0.005). The effect of metoclopramide occurred in the interval for the biopsy capsule to cross the pylorus (15.1 +/- 2.7 min versus control 60.8 +/- 16.6 min) (p less than 0.005) and in fluoroscopy time required (15.1 +/- 1.9 s versus control 46 +/- 17 s) (p less than 0.005). Oral metoclopramide is effective in reducing procedure time for small bowel biopsy, and its predictable action facilitates reduction in fluoroscopy exposure.


Subject(s)
Intestine, Small/pathology , Metoclopramide/therapeutic use , Premedication , Administration, Oral , Biopsy , Child , Child, Preschool , Female , Fluoroscopy , Humans , Infant , Infant, Newborn , Male , Random Allocation , Time Factors
17.
J Pediatr Surg ; 19(6): 848-54, 1984 Dec.
Article in English | MEDLINE | ID: mdl-6520686

ABSTRACT

Extended (18 to 24 hour) esophageal pH monitoring establishes the diagnosis of gastroesophageal reflux (GER) utilizing a pH score, and relates respiratory symptoms to GER when the mean duration of sleep reflux (ZMD) is prolonged. A disadvantage of this method is the expense of overnight hospitalization. We performed extended esophageal pH recordings in 66 consecutive children (1 week to 15 years old) being evaluated for GER. Six portions of the 18- to 24-hour esophageal pH recording were compared to the complete record in an attempt to define the relative accuracy of abbreviated monitoring periods. The abbreviated monitoring periods included the 30 minutes after apple juice feedings (30 minutes AJ), the 2 hours after apple juice feedings (2 hours PC AJ), the 2 hours after milk-formula feedings (2 hours PC MF), the 8 hours with two feedings of apple juice (8 hours AJ), the 8 hours with two feedings of milk formula (8 hours MF), and the first 12 hours of recording (1st 12 hours). The accuracy relative to the 18- to 24-hour recording was poor for 30 minutes AJ, 2 hours PC AJ, and 2 hours PC MF periods (30% to 58%). An improved accuracy occurred during 8-hour AJ periods (29/31, 94%) in children without respiratory symptoms. Although the accuracy in patients with respiratory symptoms was best during 8-hour MF (31/35, 89%) and 1st 12-hour (33/35, 94%) periods, a high false-negative rate for the ZMD (31% to 41%) during abbreviated pH monitoring indicates that many patients with reflux-induced respiratory symptoms will be unrecognized.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Esophagus/metabolism , Gastroesophageal Reflux/diagnosis , Monitoring, Physiologic/methods , Adolescent , Child , Child, Preschool , Female , Humans , Hydrogen-Ion Concentration , Infant , Infant, Newborn , Male , Time Factors
19.
Muscle Nerve ; 7(6): 486-7, 1984.
Article in English | MEDLINE | ID: mdl-6543902

ABSTRACT

Myotonic dystrophy in the neonate is commonly accompanied by facial diplegia, generalized muscular hypotonia, talipes equinovarus, and muscular respiratory failure. The gastrointestinal manifestations of this disease include poor sucking, choking, regurgitation, aspiration, and swallowing difficulties. Gastroparesis can be a major contributor to the feeding difficulties experienced by these infants. We report on an infant with congenital myotonic dystrophy in whom a severe gastric motility problem was alleviated by metoclopramide therapy. This smooth muscle manifestation may be an important and potentially remediable source of morbidity in these infants.


Subject(s)
Gastrointestinal Diseases/etiology , Gastrointestinal Motility , Myotonic Dystrophy/congenital , Female , Gastric Emptying , Gastrointestinal Diseases/drug therapy , Gastrointestinal Diseases/physiopathology , Humans , Infant, Newborn , Metoclopramide/therapeutic use , Myotonic Dystrophy/complications , Myotonic Dystrophy/drug therapy
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