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1.
Pediatr Int ; 51(6): 804-6, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19419520

ABSTRACT

BACKGROUND: The relationship between oxygen and retinopathy of prematurity (ROP) has been studied frequently, and a pulse oximeter has the potential to facilitate the control of oxygen fluctuation in neonates. The objective of the present study was to compare the incidence of threshold ROP (stage 3 requiring laser treatment and stage 4) in infants of <33 weeks gestation after implementing a new clinical O(2) management practice. METHODS: A retrospective study of data from the Kyoto First Red Cross Hospital neonatal intensive care unit (NICU) from 1 July 2004 to 31 October 2007 (closed 1 December 2006-30 March 2007 for reconstruction). A reduced oxygen protocol was implemented to maintain oxygen saturation (SpO(2)) values using a pulse oximeter between 88% and 92%. The incidence of threshold ROP in the earlier period (1 July 2004-31 December 2005) and the later period (1 January 2006-31 October 2007) were compared. RESULTS: The incidence of threshold ROP significantly decreased from 32.2% to 16.7%, after changing to the reduced oxygen protocol (P < 0.05). CONCLUSION: A significant decrease in the rate of threshold ROP in infants of <33 weeks gestation was observed after implementation of the new clinical O(2) management practice.


Subject(s)
Oxygen Inhalation Therapy/methods , Retinopathy of Prematurity/prevention & control , Birth Weight , Cross-Sectional Studies , Female , Gestational Age , Humans , Infant, Newborn , Intensive Care Units, Neonatal , Male , Oximetry , Retinopathy of Prematurity/blood , Retinopathy of Prematurity/diagnosis , Retinopathy of Prematurity/epidemiology , Retrospective Studies
2.
Cancer ; 113(6): 1362-9, 2008 Sep 15.
Article in English | MEDLINE | ID: mdl-18661511

ABSTRACT

BACKGROUND: L-asparaginase is a key drug in the treatment of childhood acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma (LBL). However, L-asparaginase can cause a fatal complication of pancreatitis, and an effective treatment for L-asparaginase-associated pancreatitis (AAP) has not been developed to date. The authors investigated whether rapidly treating children with AAP by continuous regional arterial infusion (CRAI) of protease inhibitor and antibiotic would quickly resolve AAP. METHODS: Between 2000 and 2007, 104 pediatric patients with ALL or LBL were treated at the authors' affiliated hospitals with intensive regimens that included Escherichia coli-derived L-asparaginase. Six of 104 patients developed severe AAP. One patient was treated with intravenous infusion of protease inhibitor, and the remaining 5 patients received CRAI of protease inhibitor and antibiotic within 48 hours of the onset of AAP. RESULTS: The patient who received intravenous protease inhibitor had pseudocyst formation and developed a subsequent leukemic recurrence after the interruption of chemotherapy for 4.5 months. In the other patients, AAP subsided within 2 to 6 days after the start of CRAI, and serious complications did not emerge. Significantly, chemotherapy could be resumed within 4 weeks (range, 12-23 days) after the onset of AAP, and the patients were in complete remission from 4 months to 44 months with further chemotherapy that excluded L-asparaginase. CONCLUSIONS: The current results indicated that early introduction of CRAI of protease inhibitor and antibiotic is suitable for treating severe AAP.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Antineoplastic Agents/adverse effects , Asparaginase/adverse effects , Infusions, Intra-Arterial , Pancreatic Pseudocyst/drug therapy , Pancreatitis/drug therapy , Protease Inhibitors/administration & dosage , Antineoplastic Agents/administration & dosage , Asparaginase/administration & dosage , Child , Child, Preschool , Drug Therapy, Combination , Female , Humans , Leukemia-Lymphoma, Adult T-Cell/drug therapy , Male , Neoplasm Recurrence, Local/drug therapy , Pancreatic Pseudocyst/chemically induced , Pancreatitis/chemically induced , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Survival Rate , Treatment Outcome
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