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Dive into the research topics where Robert E. Lynch is active.

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Featured researches published by Robert E. Lynch.


Clinical Toxicology | 1982

Effects of Hemodialysis and Dimercaprol in Acute Dichromate Poisoning

Eileen N. Ellis; Ben H. Brouhard; Robert E. Lynch; Earl B. Dawson; Ronald Tisdell; Myron M. Nichols; Felix Ramirez

A 22-month-old infant died after ingesting sodium dichromate his father had brought from work. Treatment included folic acid and dimercaprol administration, hemodialysis, and exchange transfusion. To evaluate this treatment, four dogs were hemodialyzed after receiving intravenous sodium dichromate: their dialyzer chromate clearance was similar to their renal chromate clearance and their dialyzer chromate clearance was not significantly different before or after dimercaprol administration. This and other cases in the literature indicate that although chromate poisoning is often fatal, supportive care, forced diuresis, and chelating agents may be helpful. Hemodialysis may be required if renal failure occurs. Awareness of toxicity and prevention remain the most important approaches.


Pediatrics | 2010

Methadone-Induced Rigid-Chest Syndrome After Substantial Overdose

Robert E. Lynch; Richard A. Hack

We report here the case of an infant who developed life-threatening rigid-chest syndrome after receiving an accidental overdose of methadone. The child responded to narcotic reversal. Pediatric physicians should be aware of this possible complication.


Pharmacology | 1983

Sodium Reabsorption during Intrarenal Diazoxide Infusion in the Dog

William Randall Allen; Ben H. Brouhard; Robert E. Lynch

Infusion of diazoxide, a potent benzothiazide antihypertensive, into the renal artery results in diuresis and natriuresis. The site within the nephron of decreased reabsorption has been controversial. Thus free flow recollection micropuncture studies of the superficial proximal tubule of the dog were undertaken to determine if diazoxide decreased sodium reabsorption from this part of the nephron. Renal blood flow, monitored by an electromagnetic flow meter, was increased by about 15% with the diazoxide infusion. Systemic blood pressure and hematocrit remained unchanged. Glomerular filtration rate increased significantly from 26 +/- 2 to 34 +/- 3 ml/min, urine flow and sodium excretion also increased (0.13 +/- 0.01 to 0.33 +/- 0.06 ml/min and 5.5 +/- 0.90 to 35.5 +/- 11.0 microEq/min, respectively). Decreased sodium reabsorption from the proximal tubule was demonstrated by a decrease in the tubular fluid to plasma inulin ratio (1.62 +/- 0.1 1.47 +/- 0.1) thus giving a reduction in fractional sodium reabsorption to the site of micropuncture (36.1 +/- 4.3 to 29.5 +/- 5.1%, p less than 0.05). To examine peritubular effects of diazoxide infusion, capillary protein concentration and pressure were measured; the former increasing significantly (9.17 +/- 0.32 to 9.80 +/- 0.35, p less than 0.05) and the latter did not change (13.1 +/- 1.0 vs. 15.2 +/- 1.4 mm Hg). Thus intrarenal diazoxide causes whole kidney vasodilatation with diuresis, natriuresis and decreased sodium reabsorption from the superficial proximal tubule. Additional studies provided no data to indicate that changes in peritubular physical factors account for the changes in sodium handling.(ABSTRACT TRUNCATED AT 250 WORDS)


Archive | 1990

Clinical Evaluation of the Kidney in Systemic and Collagen Diseases

Robert E. Lynch; Ellen G. Wood

The specialized nature of the renal vasculature and the relatively large renal blood flow make kidney damage particularly likely whenever systemic illness threatens the patient’s vascular integrity. Involvement may be minor, or kidney failure and homeostatic catastrophe may result.


Pediatrics | 1991

Captopril-induced reversible acute renal failure in an infant with coarctation of the aorta.

Ellen G. Wood; Timothy E. Bunchman; Robert E. Lynch


The Journal of Pediatrics | 1982

Membranous glomerulonephropathy with tubular dysfunction and linear tubular basement membrane IgG deposition

Ellen G. Wood; Ben H. Brouhard; Luther B. Travis; Tito Cavallo; Robert E. Lynch


Peritoneal Dialysis International | 1987

HYDROTHORAX AS A COMPLICATION OF PEDIATRIC PERITONEAL DIALYSIS

Timothy E. Bunchman; Ellen G. Wood; Robert E. Lynch


Pediatric Critical Care (Fourth Edition) | 2011

Chapter 67 – Fluid and Electrolyte Issues in Pediatric Critical Illness

Robert E. Lynch; Ellen G. Wood


Pediatric Critical Care (Third Edition) | 2006

Chapter 60 – Electrolyte Management in Pediatric Critical Illness

Ellen G. Wood; Robert E. Lynch


Pharmacology | 1983

Contents, Vol. 27, 1983

D. Mastrangelo; R. Mathison; H. Huggel; Ching-Long J. Sun; Joseph P. Hanig; Hubert F. Loyke; H.-H. Frey; W. Löscher; R. Reiche; D. Schultz; William Randall Allen; Ben H. Brouhard; Robert E. Lynch; J. Thomas Pento; Mitchell E. Johnson

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William Randall Allen

University of Texas Medical Branch

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Ching-Long J. Sun

Food and Drug Administration

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Timothy E. Bunchman

Children's National Medical Center

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Earl B. Dawson

University of Texas Medical Branch

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Eileen N. Ellis

University of Arkansas for Medical Sciences

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Felix Ramirez

University of Texas Medical Branch

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