Theo Poon-King
Northwestern University
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Featured researches published by Theo Poon-King.
The Journal of Pediatrics | 1978
Elizabeth V. Potter; Mauri Svartman; Isahak Mohammed; Reginald H Cox; Theo Poon-King; David P. Earle
Ninety-three patients with acute rheumatic fever and 195 patients with acute glomerulonephritis were observed in Trinidad during an outbreak of scabies with a high incidence of secondary streptococcal infections. Clinical and laboratory manifestations of ARF were the same as those seen in temperate zones, except that antistreptolysin O titers were less markedly increased. The patients with ARF were similar to those with AGN in respect to sex, race, location of residence, and living conditions, but were older and had markedly fewer skin infections. Currently prevalent nephritogenic streptococcal strains never were isolated from patients with ARF even when M55 streptococci appeared and led to an epidemic of AGN.
The American Journal of Medicine | 1979
Allen R. Nissenson; Richard T. Mayon-White; Elizabeth V. Potter; Valerie Mayon-White; Stella Abidh; Theo Poon-King; David P. Earle
Abstract Continued improvement was noted among 722 patients in Trinidad seven to 12 years after the onset of poststreptococcal glomerulonephritis. In the five years since earlier follow-up, two of 709 patients with previous symptomatic disease apparently had died from renal failure, and 10 patients had died from unrelated causes. Nineteen patients presently had proteinuria, three had hematuria, and three had proteinuria plus hematuria. Of these abnormalities, proteinurias in only three patients and proteinuria plus hematurias in three more patients were persistent. Thus, 0.8 per cent of the study group had persistent abnormalities. When one adds those dead with renal disease, the percentage with renal damage becomes 1.1 per cent. In addition, six patients had protein in the two urine samples obtained after assuming the lordotic position for 10 minutes and in only one of the two urine samples obtained upon rising in the morning, making 1.4 per cent with probable evidence of chronic renal disease, including the dead patients. Hypertension was present in 16 (2.3 per cent) of the patients and was much more common in those more than 20 years old (18.4 per cent). However, this prevalence of hypertension did not exceed that found in normal Trinidadians. Only three patients had serum creatinine values greater than 1.2 mg/dl. None of 13 patients with previous asymptomatic glomerulonephritis presently showed any abnormality. Thus, very few cases of chronic poststreptococcal glomerulonephritis appear to have developed in the 722 patients studied.
The Journal of Pediatrics | 1968
Elizabeth V. Potter; Alan C. Siegel; Norman M. Simon; James McAninch; David P. Earle; Theo Poon-King; Isahak Mohammed; Stella Abidh
Streptococcal cultures and antibody studies of patients during an epidemic of nephritis in Trinidad, W. I., provided evidence of a streptococcal etiology associated with impetiginous sores. Similar studies of “well” schoolchildren throughout the year revealed high incidences of sores and of streptococci in areas both with and without nephritis. The relation of these infections to antibody responses and to renal disease is considered but not completely defined.
The New England Journal of Medicine | 1978
Elizabeth V. Potter; Stella Abidh; Sharrett Ar; Burt Eg; Svartman M; Finklea Jf; Theo Poon-King; David P. Earle
To determine the incidence of chronic nephritis after poststreptococcal acute glomerulonephritis in Trinidad, 760 patients (41 adult) were examined two to six years after recovery from the illness, 344 being studied twice (four and six years). Only 1.8 per cent had persistent urine abnormalities on their last follow-up examination, and another 8.0 per cent had abnormalities that were transient or occurred only after the patient had assumed the lordotic position. In 1.4 per cent hypertension was present, whereas only one had azotemia. Both persistent urine abnormalities and hypertension increased in prevalence with age at onset of prior poststreptococcal glomerulonephritis but did not vary between sexes, races or epidemic versus endemic forms. Half the urine abnormalities present four years after recovery were absent two years later. Thus, poststreptococcal acute glomerulonephritis appears to have a low incidence of chronicity in Trinidad, with continuing resolution for more than four years.
The New England Journal of Medicine | 1967
Theo Poon-King; Isahak Mohammed; Reginald H Cox; Elizabeth V. Potter; Norman M. Simon; Alan C. Siegel; David P. Earle
The New England Journal of Medicine | 1982
Elizabeth V. Potter; Stephen A. Lipschultz; Stella Abidh; Theo Poon-King; David P. Earle
Journal of Laboratory and Clinical Medicine | 1968
Elizabeth V. Potter; Ann F. Moran; Theo Poon-King; David P. Earle
Journal of Laboratory and Clinical Medicine | 1973
Mauri Svartman; Elizabeth V. Potter; Theo Poon-King; David P. Earle
The Lancet | 1973
Theo Poon-King; Mauri Svartman; Isahak Mohammed; ElizabethV Potter; Joyce Achong; Reginald H Cox; DavidP Earle
The Journal of Infectious Diseases | 1972
Juanita P. Bray; Emma G. Burt; Elizabeth V. Potter; Theo Poon-King; David P. Earle