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1.
J Pediatr Endocrinol Metab ; 17(6): 871-7, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15270405

ABSTRACT

AIM: To determine the relative frequency of type 2 diabetes mellitus (DM) in the US, and to assess diabetes practice patterns in the US. METHOD: A questionnaire regarding pediatric diabetes practice patterns was distributed to the members of the Lawson Wilkins Pediatric Endocrine Society in 1999. Only one member of each practice group was requested to respond. Responses received through early 2000 were analyzed. RESULTS: One hundred and twenty-six practices representing 45% of the members of the Society responded. 11.9% of pediatric patients with DM were considered to have type 2 DM. On average 53 new patients with DM were seen each year. The average practice consisted of 2.5 physicians, 1.5 nurse educators, 1.3 dieticians, 1.0 social workers and 0.5 nurse practitioners. Management practices comply by and large with the recommendations of the American Diabetes Association and reflect a trend toward more intensive treatment and monitoring. CONCLUSION: Type 2 DM was seen in 11.9% of patients. Most diabetes practices in the US utilize a team approach to the management of youth with DM.


Subject(s)
Diabetes Mellitus, Type 1/drug therapy , Diabetes Mellitus, Type 2/drug therapy , Endocrinology , Pediatrics , Professional Practice , Administration, Oral , Adolescent , Adult , Aged , Blood Glucose Self-Monitoring , Child , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 2/blood , Female , Humans , Hypoglycemic Agents/administration & dosage , Hypoglycemic Agents/therapeutic use , Infant , Injections , Insulin/administration & dosage , Insulin/therapeutic use , Male , Middle Aged , Patient Care Team , Societies, Medical , Surveys and Questionnaires , Time Factors
2.
Biol Blood Marrow Transplant ; 8(10): 569-76, 2002.
Article in English | MEDLINE | ID: mdl-12434952

ABSTRACT

An optimal platelet-count threshold for prophylactic platelet transfusion in hematopoietic stem cell transplant (HSCT) recipients has yet to be determined. Between July 1997 and December 1999, we performed the first prospective randomized clinical trial addressing this issue in 159 HSCT recipients who received a prophylactic platelet transfusion when the morning platelet count fell below a 10,000/microL (10K) or 20,000/microL (20K) threshold. Subsequent prophylactic transfusions were administered according to a predetermined algorithm. The number of prophylactic and therapeutic transfusions and the incidence of minor and major bleeding were compared between the 2 groups. The groups were matched according to patient and transplantation characteristics. There were no significant differences in bleeding incidence or severity. Fourteen percent of patients in the 10K arm compared to 17% in the 20K arm had major bleeding events. Only 3 central nervous system bleeds occurred, 2 in the 10K group and 1 in the 20K group. No deaths were attributed to bleeding. An average of 11.4 days of bleeding occurred in both groups. An average of 10.4 platelet transfusions per patient were administered in the 10K group compared to 10.2 in the 20K group (P = .94). More transfusions were given above the assigned transfusion threshold in the 10K group than in the 20K group (4.3/patient versus 1.9/patient, respectively, P = .05). Safety measures incorporated into our study may have precluded demonstration of significant differences in platelet use between the groups. In conclusion, a platelet transfusion trigger of 10K was found to be safe; however, a decrease in platelet use was not achieved because of safety measures incorporated into our study design.


Subject(s)
Hematopoietic Stem Cell Transplantation/adverse effects , Hemorrhage/prevention & control , Platelet Transfusion/standards , Adolescent , Adult , Aged , Algorithms , Bone Marrow Transplantation/adverse effects , Child , Child, Preschool , Female , Hemorrhage/etiology , Hemorrhage/therapy , Humans , Incidence , Male , Middle Aged , Platelet Count , Platelet Transfusion/statistics & numerical data , Prospective Studies
3.
JAMA ; 289(18): 2393-9, 2003 May 14.
Article in English | MEDLINE | ID: mdl-12746363

ABSTRACT

CONTEXT: Although cancers occur with increased frequency in children with human immunodeficiency virus (HIV) infection, the specific clinical, immunological, and viral risk factors for malignancy have not been identified. OBJECTIVE: To identify risk factors for malignancy among HIV-infected children. DESIGN, SETTING, AND PATIENTS: A multicenter case-control study of children with HIV at 26 institutions participating in the Pediatric Oncology Group. Forty-three case patients with a new malignancy and 74 control patients without a malignancy were matched based on the duration of their infection. Patients were enrolled between January 1992 and July 1998. MAIN OUTCOME MEASURES: Clinical and laboratory factors assessed as putative risk factors included demographic characteristics, HIV characteristics, prior antiretroviral treatment, and CD4 cell count. Coviral infections with Epstein-Barr virus (EBV), cytomegalovirus, and human herpesvirus 6 were assessed by semiquantitative polymerase chain reaction assays and serological testing. RESULTS: Case malignancy diagnoses included 28 non-Hodgkin lymphoma, 4 B-cell acute lymphoblastic leukemia, 1 Hodgkin disease, 8 leiomyosarcoma, 1 hepatoblastoma, and 1 schwannoma. Epstein-Barr virus viral load of more than 50 viral genome copies per 105 peripheral blood mononuclear cells was strongly associated with cancer risk but only for children with CD4 cell counts of at least 200/ microL (odds ratio [OR], 11.33; 95% confidence interval [CI], 2.09-65.66, P<.001). High EBV viral load was not associated with cancer for children with CD4 cell counts of less than 200/ microL (OR, 1.12; 95% CI, 0.13-9.62; P =.99). Zidovudine antiretroviral therapy did not confer a significant protective effect for either the high (OR, 0.81; 95% CI, 0.22-3.09; P =.77) or the low CD4 cell count groups (OR, 0.27; 95% CI, 0.04-1.46; P =.16). The route of HIV infection was not associated with increased cancer risk. CONCLUSIONS: Route of infection, demographic characteristics, and zidovudine use were not associated with the development of malignancy in HIV-infected children. High viral burden with EBV was associated with the development of malignancy in HIV-infected children although the effect was modified by CD4 cell count. The pathogenesis of HIV-related pediatric malignancies remains unclear and other contributing risk factors can be elucidated only through further study.


Subject(s)
Epstein-Barr Virus Infections/complications , HIV Infections/complications , Lymphoma, AIDS-Related/epidemiology , Neoplasms/complications , Neoplasms/epidemiology , Antiviral Agents/therapeutic use , CD4 Lymphocyte Count , Case-Control Studies , Child , Child, Preschool , Cytomegalovirus Infections/blood , Cytomegalovirus Infections/complications , Cytomegalovirus Infections/virology , Epstein-Barr Virus Infections/blood , Epstein-Barr Virus Infections/virology , Female , HIV Infections/immunology , HIV Infections/virology , Hepatoblastoma/complications , Hepatoblastoma/epidemiology , Hepatoblastoma/etiology , Herpesvirus 6, Human , Humans , Infant , Leiomyosarcoma/complications , Leiomyosarcoma/epidemiology , Leiomyosarcoma/etiology , Lymphoma, AIDS-Related/etiology , Male , Neoplasms/etiology , Neurilemmoma/complications , Neurilemmoma/epidemiology , Neurilemmoma/etiology , Regression Analysis , Risk Factors , Roseolovirus Infections/blood , Roseolovirus Infections/complications , Roseolovirus Infections/virology , Viral Load
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