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1.
Int J Clin Pharmacol Ther ; 38(10): 492-9, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11073291

ABSTRACT

BACKGROUND AND PURPOSE: An increased incidence of post-surgical infectious complications in children admitted with a diagnosis of perforated appendicitis led to development of a disease-specific antibiogram and modification of our post-operative antibiotic regimen. METHODS: A historical control group comprised of 32 pediatric patients receiving ampicillin, gentamicin, and clindamycin (group AGC) was compared to a cohort of 32 children receiving ticarcillin/clavulanate plus gentamicin (group TG). The surgical procedure, peri-operative management, and inclusion, exclusion and discharge criteria were the same for each group. Outcome measures including length of stay, time to defervesce, incidence of infectious complications, and clinical failures to the antibiotic regimen were compared. RESULTS: The groups were similar with respect to gender, age, weight, surgical time, pre-operative leukocytes, and number of intra-operative bacterial isolates cultured per patient. Length of stay was 10.1 days in group TG and 12.5 days for group AGC (p = 0.0197). The number of clinical failures was reduced from 9 (28.1%) to 2 (6.3%) in group TG (p = 0.02). The time to defervesce was decreased by 1.4 days, and the number of infectious complications was reduced to 2.5-fold in group TG patients. CONCLUSIONS: Ticarcillin/clavulanate plus gentamicin was clinically more effective than ampicillin, gentamicin, and clindamycin combination therapy in the management of perforated appendicitis in our pediatric population.


Subject(s)
Appendicitis/drug therapy , Drug Therapy, Combination/therapeutic use , Intestinal Perforation/drug therapy , Adolescent , Ampicillin/therapeutic use , Anti-Bacterial Agents/therapeutic use , Child , Child, Preschool , Clavulanic Acids/therapeutic use , Clindamycin/therapeutic use , Gentamicins/therapeutic use , Humans , Infant , Penicillins/therapeutic use , Retrospective Studies , Ticarcillin/therapeutic use
2.
Blood ; 96(7): 2369-72, 2000 Oct 01.
Article in English | MEDLINE | ID: mdl-11001885

ABSTRACT

Chronic red blood cell transfusion can prevent many of the manifestations of sickle cell disease. The medical costs of chronic transfusion and management of associated side effects, especially iron overload, are considerable. This study was undertaken to evaluate the financial impact of chronic transfusion for stroke prevention in patients with sickle cell anemia. Outpatient charges pertaining to hospital-based Medicare uniform bill (UB-92) codes, professional fees, and iron chelation were evaluated. Data were collected on 21 patients for a total of 296 patient months (mean, 14; median, 14 months/patient). Charges ranged from $9828 to $50 852 per patient per year. UB-92, chelation, and physician-related charges accounted for 53%, 42%, and 5% of total charges, respectively. Of UB-92 charges, 58% were associated with laboratory fees and 16% were related to the processing and administration of blood. Charges for patients who required chelation therapy ranged from $31 143 to $50 852 per patient per year (mean, $39 779; median, $38 607). Deferoxamine accounted for 71% of chelation-related charges, which ranged from $12 719 to $24 845 per patient per year (mean, $20 514; median, $21 381). The financial impact of chronic transfusion therapy for sickle cell disease is substantial with charges approaching $400 000 per patient decade for patients who require deferoxamine chelation. These data should be considered in reference to cost and efficacy analyses of alternative therapies for sickle cell disease, such as allogeneic bone marrow transplantation.


Subject(s)
Anemia, Sickle Cell/complications , Erythrocyte Transfusion/economics , Health Care Costs , Stroke/prevention & control , Adolescent , Child , Cost-Benefit Analysis , Deferoxamine/therapeutic use , Erythrocyte Transfusion/adverse effects , Humans , Iron Chelating Agents/therapeutic use , Iron Overload/drug therapy , Iron Overload/etiology , Stroke/etiology , Treatment Outcome
3.
Med Pediatr Oncol ; 26(6): 405-8, 1996 Jun.
Article in English | MEDLINE | ID: mdl-8614377

ABSTRACT

In an attempt to decrease the incidence of central venous catheter sepsis in children with cancer, we conducted a study to evaluate the benefit of adding broad-spectrum antibiotics to the catheter "flush solution." In a prospective, placebo-controlled, double-blinded, randomized trial, 69 children with different types of malignancies were studied. The central venous catheters in these children were flushed with either the standard solution (normal saline + 100 U/ml of heparin) or the study solution (25 microgram/ml of both amikacin and vancomycin added to the standard solution). At the conclusion of the study, 64 children with a total of 67 indwelling central venous lines were assessable. The total catheter days on study were 20,700 days, with a median of 323 catheter days per patient. We documented 10 events of catheter-related infections (0.49 events/1,000 catheter days at risk). Five of these events were catheter-related sepsis (0.24 sepses/1,000 catheter days): two were fungal and three were bacterial. Due to the low incidence of catheter-related sepsis in this study, no statement regarding the prophylactic use of antibiotics could be made. The extremely low rate of catheter-related sepsis reported herein may be retrospectively attributed to continuous staff education regarding aseptic techniques in handling these catheters. Staff education is essential, and probably the most effective factor in preventing catheter-related sepsis.


Subject(s)
Catheterization, Central Venous/adverse effects , Catheters, Indwelling/adverse effects , Drug Therapy, Combination/therapeutic use , Staphylococcal Infections/prevention & control , Adolescent , Adult , Amikacin/therapeutic use , Anti-Bacterial Agents/therapeutic use , Candidiasis/etiology , Catheterization, Central Venous/instrumentation , Child , Child, Preschool , Double-Blind Method , Female , Heparin/therapeutic use , Humans , Incidence , Infant , Infection Control , Inservice Training , Male , Medical Staff, Hospital/education , Neoplasms/therapy , Nursing Staff, Hospital/education , Prospective Studies , Retrospective Studies , Sodium Chloride , Staphylococcal Infections/etiology , Vancomycin/therapeutic use
4.
Clin Pharm ; 9(3): 179-91, 1990 Mar.
Article in English | MEDLINE | ID: mdl-2107997

ABSTRACT

The chemistry, pharmacology, pharmacokinetics, and adverse effects of ifosfamide and mesna are described separately, followed by a discussion of the adverse effects of concurrent ifosfamide and mesna, the clinical spectrum of ifosfamide, and the dosage and administration of the two drugs. Ifosfamide, an active analogue of cyclophosphamide, differs from other direct alkylating substances in that it requires biotransformation in the liver before it can exert its alkylating effects. The bioavailability of ifosfamide after oral administration exceeds 95%. The adverse effects of ifosfamide include hematologic, urinary tract, GI tract, and CNS toxicity. Mesna is a thiol compound designed to function as a regional detoxificant of urotoxic oxazaphosphorine cytostatics such as ifosfamide. The drug is rapidly oxidized in the plasma to its dimeric form, dimesna, one third of which is converted back to mesna by glutathione reductase. The mean total urinary availability of mesna administered orally is 76%. Mesna may produce gastrointestinal and allergic reactions. The adverse effects of concurrent ifosfamide and mesna include urinary tract and renal toxicity. Although current FDA-approved labeling is limited to refractory germ cell testicular cancer, ifosfamide has also shown efficacy in the treatment of lymphoma, lung cancer, and sarcomas. Optimum dosage and scheduling remain to be determined; studies suggest that a fractionated dosage schedule provides antineoplastic activity with tolerable toxicity. Ifosfamide, used in combination with mesna for uroprotection, provides a useful therapeutic option for the management of patients with testicular cancer, soft tissue sarcomas, or high-grade malignant lymphomas.


Subject(s)
Ifosfamide/therapeutic use , Mercaptoethanol/analogs & derivatives , Mesna/therapeutic use , Neoplasms/drug therapy , Animals , Humans , Ifosfamide/adverse effects , Ifosfamide/pharmacokinetics , Mesna/adverse effects , Mesna/pharmacokinetics
6.
JAMA ; 237(21): 2299-302, 1977 May 23.
Article in English | MEDLINE | ID: mdl-576923

ABSTRACT

Mucocutaneous lymph node syndrome is a recently described entity whose principal signs and symptoms include fever, unresponsiveness to antibiotics, congested conjunctivae, reddening of the oral cavity, lips, palms, and soles, exanthem, edema, nonsuppurative cervical adenitis, and desquamation of the fingertips. Almost 7,000 cases have been reported in Japan. Analysis of the 39 cases reported in the United States reveals findings similar to those in Japan. United States cases, however, have had a higher boy-to-girl ratio (2:1), and age distribution peaks at a later time (3 years of age). We report a case with many characteristics of Rocky Mountain spotted fever, including a positive Well-Felix reaction. Some cases of mucocutaneous lymph node syndrome may be misdiagnosed as Rocky Mountain spotted fever.


Subject(s)
Lymphatic Diseases/diagnosis , Mucocutaneous Lymph Node Syndrome/diagnosis , Rocky Mountain Spotted Fever/diagnosis , Age Factors , Anti-Bacterial Agents/therapeutic use , Child , Diagnosis, Differential , Female , Humans , Mucocutaneous Lymph Node Syndrome/drug therapy , Mucocutaneous Lymph Node Syndrome/epidemiology , Rocky Mountain Spotted Fever/epidemiology , Sex Factors , United States
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