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1.
Pediatr Neurol ; 24(4): 313-6, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11377110

ABSTRACT

Subclinical rhythmic electroencephalogram (EEG) discharge is an uncommon rhythmic EEG pattern that has been reported to occur in adults. It is thought to be a nonspecific finding with little clinical significance. This article reports this EEG pattern in two children and suggests it be called subclinical rhythmic EEG discharge of adults and children.


Subject(s)
Brain/physiopathology , Electroencephalography , Hemolytic-Uremic Syndrome/physiopathology , Learning Disabilities/physiopathology , Child , Female , Hemolytic-Uremic Syndrome/complications , Hemolytic-Uremic Syndrome/diagnosis , Humans , Learning Disabilities/complications , Syndrome
2.
Gastrointest Endosc ; 46(1): 1-7, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9260697

ABSTRACT

BACKGROUND: Male alcoholics hospitalized with actively bleeding esophageal varices were treated with sclerotherapy or sham sclerotherapy and the outcomes during the index hospitalization were compared. METHODS: The 87 patients were a subset of 253 patients enrolled in a prospective, randomized, single-blind, multicenter, controlled trial conducted in 12 VA medical centers. The patients (44 sclerotherapy, 43 sham therapy) were actively bleeding from esophageal varices at either randomization endoscopy (49) or follow-up endoscopy (38). Events and resource use during the index hospitalization were recorded. RESULTS: In 40 (91%) of the sclerotherapy and 26 (60%) of the sham therapy patients, bleeding was stopped during the endoscopy session (p < 0.001). During the hospitalization, 10 (25%) sclerotherapy and 21 (49%) sham therapy patients died (p = 0.04, relative risk 2.17, 95% CI [1.02, 4.61]); 9 sclerotherapy and 22 sham therapy patients rebled (p = 0.005). The median transfusion requirement was higher for sham therapy (8 vs 4 units, p = 0.001), the number of median ICU hours was greater (101 vs 55, p < 0.001), and more patients in this group required shunt surgery (6 vs 0, p = 0.01). CONCLUSION: Sclerotherapy, compared to no sclerotherapy, stops hemorrhage from actively bleeding esophageal varices and reduces use of resources. Sclerotherapy significantly increased hospital survival.


Subject(s)
Esophageal and Gastric Varices/therapy , Gastrointestinal Hemorrhage/therapy , Liver Cirrhosis, Alcoholic/complications , Sclerotherapy , Alcoholism/complications , Endoscopy, Digestive System , Esophageal and Gastric Varices/complications , Esophageal and Gastric Varices/diagnosis , Follow-Up Studies , Gastrointestinal Hemorrhage/diagnosis , Gastrointestinal Hemorrhage/etiology , Gastrointestinal Hemorrhage/mortality , Hospital Mortality , Hospitalization , Humans , Liver Cirrhosis, Alcoholic/diagnosis , Liver Cirrhosis, Alcoholic/mortality , Male , Middle Aged , Retrospective Studies , Sclerotherapy/methods , Single-Blind Method , Treatment Outcome
3.
Radiology ; 185(1): 21-3; discussion 23-4, 1992 Oct.
Article in English | MEDLINE | ID: mdl-1523310

ABSTRACT

Ultrasound (US) of the liver surface with a high-frequency, small-parts, short-focused probe has been proposed as a method of diagnosing cirrhosis. US of the liver was performed in 50 consecutive patients undergoing diagnostic liver biopsy to assess the clinical usefulness of this noninvasive procedure in diagnosing hepatic cirrhosis. Eight patients had histologically proved cirrhosis, and 42 had no histologic evidence of cirrhosis. Seven of the eight patients with cirrhosis had a normal liver surface at US, and five of the 42 patients without cirrhosis had an abnormal liver surface. US of the liver surface with this probe was not reliable in this heterogeneous patient population.


Subject(s)
Liver Cirrhosis/diagnostic imaging , Humans , Prospective Studies , Ultrasonography
7.
Am J Perinatol ; 4(4): 365-71, 1987 Oct.
Article in English | MEDLINE | ID: mdl-3651196

ABSTRACT

The effects on fetal growth of iatrogenic prescription for dietary restriction in pregnancy have been infrequently assessed, and results have suggested large decrements in birthweight. We therefore related maternal dietary restriction to fetal growth among participants in the National Collaborative Perinatal Project at the Columbia Presbyterian Medical Center in New York. There were 255 women who delivered term infants with birthweights under the 31st percentile (low birthweight), who were each matched to women who delivered heavier term infants, within ethnic and gestational age strata. On review of antenatal records, 198 women were identified who had received a physician's recommendation to restrict caloric intake to 1800 kcal/day or below. The odds ratio between caloric restriction and low birthweight was 0.88 (not significant [NS]). Rates of maternal weight gain were controlled by linear multiple regression analysis, since higher weight gain was associated both with the likelihood of having a diet prescribed and with higher birthweight. With control for weight gain, although the odds ratio was reversed, the change was of small magnitude and not statistically significant. We found no relationship between medical advice to limit caloric intake during pregnancy and intrauterine growth retardation. Since women asked to limit caloric intake continued to gain more weight than others, the results are consistent with lack of compliance with the dietary regimen.


Subject(s)
Birth Weight , Diet Therapy/adverse effects , Embryonic and Fetal Development , Energy Intake , Fetal Growth Retardation/etiology , Adult , Body Weight , Female , Humans , Iatrogenic Disease , Infant, Newborn , Pregnancy
8.
Cancer ; 60(5): 1107-10, 1987 Sep 01.
Article in English | MEDLINE | ID: mdl-3038298

ABSTRACT

The male-female ratio in 186 hepatocellular carcinoma (HCC) Chinese patients was 5:1. The clinical presentation, biochemical parameters, and histologic findings were the same in both sexes except for a higher proportion of underlying cirrhosis (P = 0.02), and spider naevi (P = 0.04) in the men. There were also more smokers and alcohol drinkers among the men. Over 75% of both sexes were positive for the hepatitis B surface antigen. The possible contributory factors to the predominance of males to females in HCC included: the association with the hepatitis B virus, the higher proportion of male cirrhotics, smoking, and alcohol drinking. The survival probability for both sexes was equally poor; the median survival was 8 weeks for males and 10 weeks for females.


Subject(s)
Carcinoma, Hepatocellular/epidemiology , Liver Neoplasms/epidemiology , Sex Factors , Actuarial Analysis , Alcohol Drinking , Carcinoma, Hepatocellular/mortality , Carcinoma, Hepatocellular/pathology , China/ethnology , Female , Hepatitis B Surface Antigens/analysis , Hong Kong , Humans , Liver Cirrhosis/pathology , Liver Neoplasms/mortality , Liver Neoplasms/pathology , Male , Middle Aged , Smoking
9.
Antimicrob Agents Chemother ; 29(1): 122-6, 1986 Jan.
Article in English | MEDLINE | ID: mdl-3524420

ABSTRACT

Five patients with chronic hepatitis B were treated with 8-day courses of leukocyte (alpha) interferon (5 X 10(6) U/day) and with 8-day courses of recombinant fibroblast (betaser) interferon at dosages of 5 X 10(6), 35 X 10(6), and 105 X 10(6) U/day. Inhibition of hepatitis B virus replication as evidenced by a decrease in DNA polymerase (DNAP) activity was seen during all treatment courses. Equivalent reduction in DNAP was seen from the low-dose alpha and beta ser regimens, but beta ser interferon at 35 X 10(6) U/day achieved a significantly greater decrease in DNAP activity than did the low-dose regimens. In no patient, however, was permanent loss of DNAP noted. Because of dose-limiting toxicity, only two patients were escalated to the 105 X 10(6)-U/day dosage level. Transient proteinuria was noted in two patients while they were receiving interferon. This has not been noted in other patients receiving this preparation and could not be explained by the development of anti-interferon antibodies. This study has defined an appropriate dosage for future longer-term trials of this agent alone and in combination with other antivirals for the treatment of chronic hepatitis B.


Subject(s)
Hepatitis B/therapy , Interferon Type I/therapeutic use , Interferon-beta , Recombinant Proteins/therapeutic use , Adult , Clinical Trials as Topic , Female , Hepatitis B Surface Antigens/analysis , Humans , Interferon Type I/adverse effects , Interferon beta-1a , Interferon beta-1b , Male , Middle Aged , Random Allocation , Recombinant Proteins/adverse effects
11.
J Ultrasound Med ; 3(12): 557-61, 1984 Dec.
Article in English | MEDLINE | ID: mdl-6392587

ABSTRACT

A study measuring two quantitative parameters of human liver in vivo was performed to assess the reliability of measurement of the two parameters, and to evaluate their potential for diagnosing and grading diffuse fibrotic liver disease. The parameters measured were attenuation and "mean scatterer spacing," a measure of tissue structure. Components of variance analysis demonstrated that variation in the measured parameters was a function of the subject being examined, with significant variation noted between data acquisition sessions performed the same day. There was no significant additional variation of the measurements from week to week over a one-month period. A good correlation of the parameters with the severity of liver disease indicates that the technique may be useful in the clinical evaluation of diffuse liver disease.


Subject(s)
Liver/anatomy & histology , Ultrasonography , Analysis of Variance , Humans , Liver/pathology , Liver Diseases/diagnosis
12.
Ann Intern Med ; 101(5): 613-6, 1984 Nov.
Article in English | MEDLINE | ID: mdl-6486592

ABSTRACT

Survival data from 379 patients with chronic hepatitis B were analyzed to determine life expectancy for the patient from the time of first contact. One hundred twenty-one patients had chronic persistent hepatitis, 128 had chronic active hepatitis, and 130 had chronic active hepatitis with cirrhosis. The frequency of symptoms (p less than 0.001), stigmata of chronic liver disease (p less than 0.001), and liver function test abnormalities (p less than 0.001) increased as the histologic features worsened, whereas the percentage of patients with circulating hepatitis B DNA polymerase declined (p less than 0.001). Women were uncommon in our series and had less severe disease than men (p less than 0.02). Fifty-one patients had died by the time of this analysis. The estimated 5-year survival rates were 97% for patients with chronic persistent hepatitis, 86% for those with chronic active hepatitis, and 55% for those with chronic active hepatitis with cirrhosis. The usual cause of death was liver failure and its sequelae. A multivariate analysis found age of 40 years or more, total bilirubin level of 1.5 mg/dL or more, ascites, and spider nevi to be factors that identified patients at a higher risk of death. The prognosis for patients with chronic hepatitis B is similar to that for patients with chronic hepatitis of other causes.


Subject(s)
Hepatitis B/mortality , Hepatitis, Chronic/mortality , Adult , Female , Hepatitis B/complications , Hepatitis B/pathology , Hepatitis B Surface Antigens/analysis , Hepatitis, Chronic/complications , Hepatitis, Chronic/pathology , Humans , Liver Cirrhosis/etiology , Male , Prognosis , Sex Factors
15.
J Infect Dis ; 148(5): 907-13, 1983 Nov.
Article in English | MEDLINE | ID: mdl-6631076

ABSTRACT

The clinical, virologic, biochemical, and immunologic effects of a biosynthetic human leukocyte interferon, recombinant leukocyte A interferon (rIFN-A or HuIFN-alpha 2) are reported in nine patients with chronic hepatitis B virus infection and circulating Dane particle-associated polymerase activity. Eight-day courses of rIFN-A were given starting at a dose of 3 X 10(6) units per day and reaching 68 X 10(6) units per day in two patients. Major toxic side effects included fever, fatigue, gastrointestinal symptoms, myalgias, and headache. Most courses of rIFN-A were associated with a reduction in Dane particle-associated polymerase activity, but in no case was this change permanent. There were also changes in lymphocyte subpopulations at the higher dosage levels of rIFN-A. Because of the reproducible, statistically significant effect on viral replication, further study with this and other biosynthetic interferon species is warranted.


Subject(s)
Hepatitis B virus/drug effects , Hepatitis B/therapy , Interferon Type I/therapeutic use , Adult , Aged , Chronic Disease , DNA, Recombinant , DNA-Directed DNA Polymerase/metabolism , Dose-Response Relationship, Drug , Female , Hepatitis B/blood , Hepatitis B/microbiology , Hepatitis B virus/enzymology , Humans , Interferon Type I/adverse effects , Interferon Type I/blood , Leukocyte Count , Liver Function Tests , Male , Middle Aged
16.
Gastroenterology ; 84(2): 388-93, 1983 Feb.
Article in English | MEDLINE | ID: mdl-6848412

ABSTRACT

A prospective blinded study comparing the indium 111 leukocyte scan to barium enema, colonoscopy, or surgery or a combination of these, was carried out in 15 patients (10 with active ulcerative colitis and 5 with active Crohn's colitis). Correlation of disease location to colonic regions between indium scan and other diagnostic studies was excellent in 11 instances, good in 2, and poor in 3. In 2 of the 3 studies where major disagreement occurred, the comparative barium enema was performed greater than 2 mo after the indium scan. Disease activity, estimated by the intensity of radionuclide uptake, was compared to clinical disease activity assessed by the Crohn's Disease Activity Index for both forms of colitis. The relative degree of inflammation estimated by the indium scan correlated well with the independent clinical assessment (correlation coefficient = 0.81). The indium 111 leukocyte scan appears to be an accurate, noninvasive method for assessing the extent and the severity of the inflammation in patients with acute ulcerative or Crohn's colitis.


Subject(s)
Colitis, Ulcerative/diagnostic imaging , Crohn Disease/diagnostic imaging , Indium , Leukocytes , Radioisotopes , Adolescent , Adult , Barium Sulfate , Colitis, Ulcerative/diagnosis , Colonoscopy , Crohn Disease/diagnosis , Enema , Female , Humans , Male , Middle Aged , Prospective Studies , Radionuclide Imaging
18.
Am J Med ; 73(1A): 267-70, 1982 Jul 20.
Article in English | MEDLINE | ID: mdl-7102705

ABSTRACT

Three patients with HBsAg-positive and DNA-polymerase-positive chronic hepatitis were treated with increasing dosages of intravenous acyclovir. A fall in DNA polymerase activity was seen with all courses of acyclovir but no dose-response relationship was evident. In only one patient did DNA polymerase fall to zero where it has remained for five months. Two out of 10 courses were associated with significant side effects with the highest dosages of acyclovir but these promptly resolved when the agent was stopped. Acyclovir's apparently partial and transient action suggests that it will not have a role in the treatment of chronic hepatitis B virus infection.


Subject(s)
Antiviral Agents/therapeutic use , Guanine/analogs & derivatives , Hepatitis B/drug therapy , Acyclovir , Antiviral Agents/adverse effects , Chronic Disease , DNA-Directed DNA Polymerase/metabolism , Drug Evaluation , Guanine/adverse effects , Guanine/therapeutic use , Hepatitis B virus/enzymology , Humans
19.
Ann Intern Med ; 96(5): 565-9, 1982 May.
Article in English | MEDLINE | ID: mdl-7041728

ABSTRACT

Sixty patients with active upper gastrointestinal bleeding were randomized to received either continuous intravenous infusions of vasopressin (29 patients) or placebo (31 patients) at a rate of 40 U/h. Six hours after beginning the study, 13 patients in the vasopressin group and 11 in the placebo group] had ceased bleeding (p = 0.46). By 24 hours. 17 patients in the vasopressin group and 14 in the placebo group had stopped bleeding (p = 0.30). Restriction of the analysis to patients bleeding from varices showed no advantage with vasopressin treatment after 6 or 24 hours. No consistent trend favoring use of vasopressin to stop hemorrhage was noted during the 30-month study period. There was little difference between the two groups in the number of patients needing surgery (13 on vasopressin, 18 on placebo; p = 0.30) or the number of deaths (eight on vasopressin, 11 on placebo; p = 0.51); the transfusion requirement was the same. In our patients, a continuous intravenous infusion of vasopressin neither controlled bleeding nor altered outcome.


Subject(s)
Gastrointestinal Hemorrhage/drug therapy , Vasopressins/administration & dosage , Clinical Trials as Topic , Female , Humans , Infusions, Parenteral , Male , Middle Aged , Placebos , Random Allocation , Vasopressins/adverse effects
20.
JAMA ; 247(16): 2261-5, 1982 Apr 23.
Article in English | MEDLINE | ID: mdl-6175774

ABSTRACT

Ten young adult patients with chronic hepatitis B virus infection and positive hepatitis B e antigen and DNA polymerase (DNAP) levels were treated with alternating courses of seven to 28 days of 5 to 7.5 mg/kg of vidarabine monophosphate (adenine arabinoside monophosphate) and 28 days of human leukocyte interferon (IFN-alpha); three different regimens were given on an outpatient basis. All patients with a fall in their DNAP level, and the DNAP remained undetectable six months after treatment was stopped in one patient. The major side effect, which most often occurred in those patients receiving 7.5 mg/kg of vidarabine monophosphate, was severe muscular pains. This study demonstrated the feasibility of administering vidarabine monophosphate and interferon to outpatients. Based on data from this and other studies, it is now possible to use a relatively nontoxic regimen that includes 28 days of 5 mg/kg of vidarabine monophosphate in a larger controlled study to answer the question of efficacy.


Subject(s)
Arabinonucleotides/therapeutic use , Hepatitis B/therapy , Interferons/therapeutic use , Vidarabine Phosphate/therapeutic use , Adult , Chronic Disease , Clinical Trials as Topic , DNA-Directed DNA Polymerase/analysis , Double-Blind Method , Hepatitis B/immunology , Hepatitis B Surface Antigens/analysis , Hepatitis B e Antigens/analysis , Humans , Male , Random Allocation , Vidarabine Phosphate/adverse effects
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