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Featured researches published by A. Mondal.


Annals of Internal Medicine | 1969

Replacement of Water and Electrolyte Losses in Cholera by an Oral Glucose—Electrolyte Solution

Nathaniel F. Pierce; Sack Rb; R. Mitra; John G. Banwell; Brigham Kl; Fedson Ds; A. Mondal

Abstract The efficacy of an orally administered glucose-electrolyte solution in replacing stool losses of water and electrolytes in severe cholera was evaluated. After initial intravenous rehydrati...


Journal of Clinical Investigation | 1970

Intestinal fluid and electrolyte transport in human cholera.

John G. Banwell; Nathaniel F. Pierce; R. Mitra; K. L. Brigham; George J. Caranasos; Keimowitz Ri; Fedson Ds; Jacob Thomas; Sherwood L. Gorbach; Sack Rb; A. Mondal

The site, nature, magnitude, and duration of fluid and electrolyte loss into the small intestine during the acute and recovery phase of human cholera was defined in 27 Indian patients. 11 subjects without cholera served as controls. The marker perfusion technique employed was shown, in preliminary experiments, to measure accurately jejunal and ileal fluid and electrolyte transmucosal transport rates under conditions of cholera diarrhea. Fluid loss into the lumen occurred from jejunal and ileal mucosa. The fluid was isotonic in both regions. Bicarbonate concentration was significantly higher in ileal than jejunal fluid during all phases of the disease. Bicarbonate concentration in both regions was significantly higher in acute cholera than during convalescence. Fluid loss into the intestinal lumen ranged from 0.07 to 10.9 ml/hr per cm. Losses were significantly greater from jejunum than ileum. Net ileal absorption was recorded in five of 10 acute cholera studies. During the acute phase of the disease, net jejunal fluid transport showed a positive correlation with fasting intestinal flow rate and stool output. Stool output was also positively correlated with jejunal fasting intestinal flow rates. Recovery of normal fluid and electrolyte absorptive function was usually complete in both jejunum and ileum by the sixth day after admission. These findings in human cholera validate the animal models of choleraic diarrhea and suggest that similar measurements of small intestinal secretory function in other nonspecific diarrheal diseases using the marker perfusion technique may be rewarding.


Journal of Clinical Investigation | 1971

Acute undifferentiated human diarrhea in the tropics: II. Alterations in intestinal fluid and electrolyte movements

John G. Banwell; Sherwood L. Gorbach; Nathaniel F. Pierce; R. Mitra; A. Mondal

The nature and magnitude of fluid and electrolyte loss into the small intestine were defined by the marker perfusion technique in patients with acute undifferentiated diarrhea (AUD) in the tropics. The patients were divided into two groups according to their small bowel bacteriologic findings, namely those with a predominant Escherichia coli flora and those with a mixed flora. 11 normal subjects served as controls. Net jejunal fluid secretion occurred into the lumen in four of seven patients with E. coli flora and three of seven with a mixed flora. The magnitude of secretion in the jejunum was greater in the E. coli flora patients than in those with a mixed flora. Four E. coli patients and one mixed flora patient had net fluid secretion in the ileum, although the magnitude of secretion in this area was less than in the jejunum. Intestinal fluid had higher bicarbonate concentration in the ileum than in the jejunum but was isotonic in both regions. It resembled in composition fluid from the same region of intestine in normal individuals. Recovery of normal fluid and electrolyte absorptive function was usually complete in both jejunum and ileum by 6-8 days after onset of the disease. Increase in unidirectional flux rates for H(3)O and (24)Na occurred in acute E. coli flora diarrhea and returned to normal levels in recovery: increase in J(beta) (plasma to lumen flux) primarily accounted for the increase in fluid loss. Intestinal biopsy revealed no alterations in villous architecture.A relationship between small bowel fluid production and the presence of toxigenic strains of E. coli within the small bowel has been found for E. coli flora patients. In many respects this disease resembles acute cholera. The mixed flora group represents a less defined entity which requires further study.


Annals of Internal Medicine | 1970

The Ventilatory Response to Acute Base Deficit in Humans: Time Course During Development and Correction of Metabolic Acidosis

Nathaniel F. Pierce; Fedson Ds; Brigham Kl; R. Mitra; Sack Rb; A. Mondal

Abstract The time courses of ventilatory response to the development and correction of acute base-deficit acidosis were studied in 35 patients with cholera. In normal controls and during stable bas...


Bulletin of The World Health Organization | 1970

The use of oral replacement solutions in the treatment of choleraand other severe diarrhoeal disorders.

R. B. Sack; J. Cassells; R. Mitra; C. Merritt; T. Butler; J. Thomas; B. Jacobs; A. Chaudhuri; A. Mondal


Pediatrics | 1970

Water and electrolyte losses due to cholera in infants and small children: a recovery balance study.

Dilip Mahalanabis; Craig K. Wallace; Ronald J. Kallen; A. Mondal; Nathaniel F. Pierce


Journal of Tropical Pediatrics | 1974

Use of an oral glucose-electrolyte solution in the treatment of paediatric cholera - a controlled study

D. Mahalanabis; R. B. Sack; B. Jacobs; A. Mondal; J. Thomas


Annals of Internal Medicine | 1970

Convalescent Carriers of Vibrio cholerae: Detection and Detailed Investigation

Nathaniel F. Pierce; John G. Banwell; Sherwood L. Gorbach; R. Mitra; A. Mondal


The Journal of Infectious Diseases | 1970

Magnitude and Duration of Antitoxic Response to Human Infection with Vibrio cholerae

Nathaniel F. Pierce; J. G. Banwell; R. Bradley Sack; R. Mitra; A. Mondal


Indian Journal of Medical Research | 1968

Preliminary results of a study of small intestinal water and solute movement in acute and convalescent human cholera.

J. G. Banwell; Nathaniel F. Pierce; R. Mitra; G. J. Caranasos; R. I. Keimowitz; A. Mondal; P. M. Manji

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R. Mitra

Johns Hopkins University

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John G. Banwell

Johns Hopkins University School of Medicine

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Jacob Thomas

Johns Hopkins University School of Medicine

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B. Jacobs

Johns Hopkins University

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D. Mahalanabis

Johns Hopkins University

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J. G. Banwell

Johns Hopkins University

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J. Thomas

Johns Hopkins University

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K. L. Brigham

Johns Hopkins University

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