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1.
Anesth Analg ; 90(4): 801-7, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10735779

ABSTRACT

UNLABELLED: Hetastarch is used for intravascular volume expansion in cardiac surgery. Studies show conflicting effects of intraoperative hetastarch administration on postoperative bleeding. Hetastarch was routinely used for volume expansion during cardiovascular surgeries at our institution until its use was discontinued intraoperatively. We performed a retrospective chart review on patients undergoing primary coronary artery bypass grafting, valve repair or replacement requiring cardiopulmonary bypass (n = 444), 234 of which received intraoperative hetastarch and 210 did not. There was no difference in demographics, cardiac surgery, or cardiopulmonary bypass duration between the two groups. Blood loss for 0-4 h postoperatively was 377 +/- 244 mL in the group not receiving hetastarch compared with 515 +/- 336 mL in the group that received hetastarch (P < 0.001). For 0-24 h postoperatively, blood loss was 923 +/- 473 mL versus 1,283 +/- 686 mL in the absence and presence of hetastarch, respectively (P < 0.001). Allogeneic transfusion requirements (cryoprecipitate, fresh frozen plasma, and platelets) were larger in the hetastarch group (all P < 0.001). Nearly all (99%) patients in the hetastarch group received less than the manufacturer's recommended dose (20 mL/kg) of hetastarch. IMPLICATIONS: Our large retrospective study suggests that intraoperative use of hetastarch in primary cardiac surgery with cardiopulmonary bypass may increase bleeding and transfusion requirements. A large prospective study is needed to determine if intraoperative administration of hetastarch should be avoided during cardiovascular surgery.


Subject(s)
Blood Transfusion , Cardiopulmonary Bypass , Hydroxyethyl Starch Derivatives/adverse effects , Plasma Substitutes/adverse effects , Postoperative Hemorrhage/chemically induced , Aged , Female , Humans , Male , Middle Aged , Multivariate Analysis , Retrospective Studies
2.
J Clin Apher ; 14(4): 185-7, 1999.
Article in English | MEDLINE | ID: mdl-10611629

ABSTRACT

Idiopathic IgA nephropathy is widely regarded as a slowly progressive disease that not infrequently results in end-stage renal failure. Only a minority of patients present with either a rapidly progressive form of glomerulonephritis, or with end-stage renal failure. Anecdotal reports of improved renal function after treatment with plasmapheresis have been published, but the efficacy of this therapy remains controversial. We describe the course of two young males presenting with uremia, hypertension, nephrotic-range proteinuria, and crescentic glomerulonephritis on renal biopsy. Both patients underwent therapy with steroids, immunosuppressive agents, and plasmapheresis without an appreciable improvement in renal function. A review of the literature does not offer any conclusive data to support the role of plasmapheresis in the treatment of rapidly progressive glomerulonephritis due to IgA nephropathy and points out the need to define criteria that may identify subsets of patients with this disorder who may potentially benefit from plasma exchange therapy. J. Clin. Apheresis 14:185-187, 1999. Published 1999 Wiley-Liss, Inc.


Subject(s)
Glomerulonephritis, IGA/therapy , Plasmapheresis , Adolescent , Adult , Combined Modality Therapy , Cyclophosphamide/therapeutic use , Glomerulonephritis, IGA/complications , Glomerulonephritis, IGA/drug therapy , Humans , Immunosuppressive Agents/therapeutic use , Kidney Failure, Chronic/etiology , Male , Prednisone/therapeutic use , Renal Dialysis , Treatment Failure
3.
AIDS Res Hum Retroviruses ; 15(9): 837-45, 1999 Jun 10.
Article in English | MEDLINE | ID: mdl-10381172

ABSTRACT

Antigenic stimulation from invasive bacterial infections, and the vaccines designed to prevent them, may promote T cell activation and enhancement of HIV-1 replication. Changes in viral load have been correlated with antigen-specific responses. We prospectively determined the impact of immunization with 23-valent pneumococcal vaccine (PVAX) and Haemophilus influenzae type b (Hib)-modified diphtheria toxoid CRM197 (DT) vaccine on HIV-1 replication in recent HIV-1 seroconverters (n = 14; median, 5.5 months from infection; median CD4+ T cells, 535 microl), and correlated results with vaccine-related immune activation. Specific antibody responses, markers of CD4+ T cell activation (transferrin and interleukin 2 receptors), and viral burden were measured at weeks -2 (pre), 0, 1, 2, 6, and 12 after immunization. By week 2, levels of IgG had increased significantly over baseline in both HIV-1-infected patients and HIV-1-seronegative control subjects (n = 9) for each antigen (geometric mean fold rise: PVAX, 10.1 versus 5.3; Hib, 16.0 versus 11.7; and DT, 26.2 versus 24.5, respectively). Despite these vigorous responses to both polysaccharide and protein antigens, HIV-1-infected patients showed limited evidence of CD4+ T cell activation at 1 week, no consistent rise in HIV-1 burden at any point, and no decline in CD4+ T cell number over time. We conclude that recent HIV-1 seroconverters show vigorous humoral responses to vaccine antigens and limited early evidence of T cell activation, but no substantial or sustained increase in viral replication or decline in CD4+ T cell number. Thus, respiratory bacterial vaccines appear immunogenic and safe early in HIV-1 infection.


Subject(s)
Bacterial Vaccines/immunology , Diphtheria Toxoid/immunology , HIV Seropositivity/immunology , HIV Seropositivity/virology , HIV-1/physiology , Haemophilus Vaccines/immunology , Vaccines, Conjugate/immunology , Adult , CD4-Positive T-Lymphocytes/immunology , CD8-Positive T-Lymphocytes/immunology , Female , HIV Seropositivity/blood , HIV-1/genetics , Humans , Male , Plasma/virology , Pneumococcal Vaccines , Prospective Studies , Vaccination , Viral Load
4.
Am J Trop Med Hyg ; 60(5): 758-66, 1999 May.
Article in English | MEDLINE | ID: mdl-10344649

ABSTRACT

To investigate reports on war-related morbidity, 527 active-duty Gulf War veterans and 970 nondeployed veterans from 14 Seabee commands were studied in 1994 with a questionnaire, sera collection, handgrip strength, and pulmonary function testing. The questionnaire assessed postwar symptoms, war exposures, and screened for chronic fatigue syndrome, post-traumatic stress disorder, and psychological symptoms suggesting neurosis (Hopkins Symptom Checklist). Sera were tested with four nonspecific reactant assays: C-reactive protein, transferrin, ferritin, and haptoglobin. Gulf War veterans reported a higher prevalence for 35 of 41 symptoms, scored higher on psychological symptom scales, were more likely to screen for post-traumatic stress disorder, had lower handgrip strength, and had higher serum ferritin assay results. Numerous comparisons of these morbidity outcomes with 30 self-reported exposures demonstrated many associations, but no unique exposure or group of exposures were implicated. Morbidity data are consistent with other postwar observations, but the etiology for morbidity findings remains uncertain.


Subject(s)
Anxiety Disorders/epidemiology , Military Personnel , Persian Gulf Syndrome/epidemiology , Veterans , Adult , Biomarkers/blood , Fatigue Syndrome, Chronic/epidemiology , Female , Ferritins/blood , Hand Strength , Humans , Male , Military Medicine , Military Personnel/psychology , Respiratory Function Tests , Stress Disorders, Post-Traumatic/epidemiology , Surveys and Questionnaires , Veterans/psychology
5.
J Am Acad Dermatol ; 37(3 Pt 1): 430-7, 1997 Sep.
Article in English | MEDLINE | ID: mdl-9308559

ABSTRACT

BACKGROUND: Increased expression of p53 has been found in the majority of basal cell carcinomas (BCCs); however, UV-light-induced signature mutations are present in only about 50% of cases. Increased nuclear staining with an immunohistochemical marker of proliferation, proliferating cell nuclear antigen (PCNA), has been correlated with aggressive behavior in BCC. OBJECTIVE: Our purpose was to determine whether there is any relationship between different histologic variants of BCC and their expression of p53, PCNA, and Ki-67. METHODS: We used immunohistochemical stains for p53, PCNA, and Ki-67, in superficial-multicentric, nodular-noduloulcerative, sclerosing, infiltrative, and metatypical BCC, to determine whether the staining patterns differ in these different histologic variants of BCC. RESULTS: Superficial-multicentric BCCs were negative for p53 in four of eight tumors. Nodular BCC showed moderately intense p53 nuclear staining with some peripheral accentuation. PCNA nuclear staining was greater than Ki-67, and PCNA-positive cells were fewer than 10% in nodular BCC. Sclerosing and infiltrative BCC showed intense p53 nuclear staining with peripheral accentuation. PCNA nuclear staining was greater than Ki-67, and PCNA-positive cells were greater than 30% in the majority of these tumors. Metatypical BCCs showed diffuse intense p53 staining. PCNA nuclear staining was greater than Ki-67, and PCNA-positive cells were greater than 30% in all tumors studied. When overlying actinic keratoses showed p53 staining, the staining did not necessarily correlate with the intensity or even the presence of positive staining in the subjacent BCC. CONCLUSION: There are at least four distinctive patterns for staining of p53, PCNA, and Ki-67 that correlate with different histologic variants of BCC.


Subject(s)
Biomarkers, Tumor/analysis , Carcinoma, Basal Cell/pathology , Ki-67 Antigen/analysis , Proliferating Cell Nuclear Antigen/analysis , Skin Neoplasms/pathology , Tumor Suppressor Protein p53/analysis , Carcinoma, Basal Cell/classification , Carcinoma, Basal Cell/metabolism , Humans , Immunohistochemistry , Neoplasm Proteins/analysis , Skin Neoplasms/classification , Skin Neoplasms/metabolism
7.
Am J Orthop (Belle Mead NJ) ; 24(2): 165-7, 1995 Feb.
Article in English | MEDLINE | ID: mdl-7613981

ABSTRACT

An unusual complication of Paget's disease is described wherein the extensor mechanism of the knee joint was disrupted because of avulsion of the patellar tendon from the tibial tubercle in a region of pagetic bone. The patient underwent successful surgical treatment of this condition.


Subject(s)
Knee Injuries/etiology , Osteitis Deformans/complications , Patella/surgery , Tendons/surgery , Adult , Humans , Knee Injuries/diagnostic imaging , Knee Injuries/surgery , Male , Osteitis Deformans/pathology , Osteitis Deformans/surgery , Patella/diagnostic imaging , Patella/pathology , Radiography , Tendons/diagnostic imaging , Tendons/pathology
8.
Am J Pediatr Hematol Oncol ; 15(4): 427-9, 1993 Nov.
Article in English | MEDLINE | ID: mdl-8214367

ABSTRACT

PURPOSE: Maffucci's syndrome is a nonhereditary congenital disorder associated with multiple enchondromas, soft tissue hemangiomas, or lymphangiomas. It carries an associated high risk of the development of malignant neoplasms, particularly sarcomatous transformation of an enchondroma, as well as other malignant mesodermal and nonmesodermal neoplasms. Hematopoietic malignancies arising in Maffucci's syndrome are exceedingly rare. We report the case of a 14-year-old girl with Maffucci's syndrome who developed acute lymphoid leukemia. PATIENTS AND METHODS: The patient presented at 18 months of age with enchondromatosis. Maffucci's syndrome was established at 10 years of age after the appearance of multiple hemangiomas. RESULTS: At 14 years of age the patient developed fatigue, frequent nosebleeds, easy bruising, and weight loss, with circulating blasts in the peripheral blood. Bone marrow examination showed replacement of marrow spaces with leukemic blasts. Immunohistochemical and flow cytometric findings were consistent with a diagnosis of acute lymphoblastic leukemia with myeloid antigen expression. CONCLUSIONS: The occurrence of acute leukemia in a patient with Maffucci's syndrome may represent predisposition to yet another malignancy and reflect further expression of a generalized mesodermal dysplasia in these patients. It also emphasizes the need for aggressive surveillance in patients with Maffucci's syndrome.


Subject(s)
Enchondromatosis/complications , Precursor Cell Lymphoblastic Leukemia-Lymphoma/complications , Adolescent , Antigens, CD/blood , Bone Marrow/pathology , Enchondromatosis/diagnostic imaging , Enchondromatosis/pathology , Female , Hemangioma/complications , Hemangioma/pathology , Humans , Lymphocytes/immunology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/blood , Precursor Cell Lymphoblastic Leukemia-Lymphoma/immunology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology , Radiography , Skin Neoplasms/complications , Skin Neoplasms/pathology
9.
J Infect Dis ; 166(5): 1149-53, 1992 Nov.
Article in English | MEDLINE | ID: mdl-1402028

ABSTRACT

Initial CD4 lymphocyte counts were studied in 244 patients with human immunodeficiency virus (HIV) seroconversion. The CD4 cell counts at initial presentation after seroconversion were normally distributed (mean, 579/mm3; SD, 252). The mean percentage of CD4 cells was 26.1% (SD, 5.6). CD4 cell counts were < 500/mm3 in 41% and < 200/mm3 in 4%. The mean calculated duration of HIV infection was 7.7 months, which was not significantly different between the highest and lowest CD4 count quartiles (8.1 vs. 7.9). Age, sex, race, and serologic evidence of toxoplasmosis, cytomegalovirus, hepatitis B, syphilis, and varicella-zoster virus were not associated with initial low CD4 cell counts; however, never-married men were significantly overrepresented in the lowest quartile. These findings suggest that extensive CD4 lymphocyte depletion is common in early HIV infection and that frequent screening is necessary to identify newly infected patients who would benefit from antiretroviral therapy.


Subject(s)
CD4 Antigens/immunology , HIV Infections/immunology , HIV Seropositivity/immunology , T-Lymphocyte Subsets/immunology , Adult , Enzyme-Linked Immunosorbent Assay , Female , Follow-Up Studies , HIV Infections/complications , Hepatitis B/complications , Hepatitis B Antibodies/blood , Hepatitis B Surface Antigens/blood , Humans , Leukocyte Count , Male , Military Personnel , Registries , Syphilis/complications , Toxoplasmosis/complications , United States
10.
Obstet Gynecol ; 77(1): 156-9, 1991 Jan.
Article in English | MEDLINE | ID: mdl-1845778

ABSTRACT

Two women with extramammary Paget disease of the vulva were given fluorescein intravenously in order to visualize disease margins with the use of an ultraviolet light. As a diagnostic modality, the technique was found to have a positive predictive value of 97.4% and a negative predictive value of 99.9%. The accuracy of the fluorescein technique was compared with gross visualization using a histologic mapping technique. A total of 2424 fields were mapped and the predictive accuracy of each test was determined. A chi 2 test demonstrated fluorescein visualization to be a significantly better predictor of a disease state. Fluorescein visualization is suggested as an adjunct to surgical management of patients with primary vulvar Paget disease.


Subject(s)
Fluoresceins , Paget Disease, Extramammary/pathology , Vulvar Neoplasms/pathology , Female , Fluorescein , Humans , Paget Disease, Extramammary/surgery , Vulvar Neoplasms/surgery
11.
Am J Clin Pathol ; 87(3): 389-91, 1987 Mar.
Article in English | MEDLINE | ID: mdl-3826005

ABSTRACT

Alpha-thalassemia can be diagnosed in the neonate based on the level of Bart's Hemoglobin (HbB) in cord blood. This level corresponds to the degree of alpha-gene deletion. Thus, the extent of the alpha-thalassemia carrier state can be determined. This is important for genetic counseling. Because HbB is present only until a child is six months of age, and the hematologic manifestations of the carrier state may be mild, early detection is important. This study identified a logarithmic relationship between the mean corpuscular volume (MCV) and HbB. Additionally, a discrimination level of 93.5 fL. was calculated to screen for neonates that required evaluation with hemoglobin electrophoresis to identify two- and possibly three-gene deletion alpha-thalassemia. The red blood cell indices were found not to be useful in identifying patients with a one-gene deletion alpha-thalassemia.


Subject(s)
Genetic Carrier Screening/methods , Thalassemia/genetics , Erythrocyte Indices , Fetal Blood/analysis , Genetic Testing/methods , Hemoglobins, Abnormal/analysis , Humans , Infant, Newborn
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