1.Influence of Pre-operative Fasting Time on Blood Glucose in Older Patients.
Journal of Korean Academy of Nursing 2011;41(2):157-164
PURPOSE: This study was performed to identify changes in blood glucose at preoperative fasting time in surgical patients over 60 yr. METHODS: Data collection was performed from July, 2008 through July, 2009. Participants consisted of 80 nondiabetic surgical patients. Blood glucose was checked from 3 to 5 times. The 5 times were 2-hr fasting on the pre-operative day (T1, n=80), 8 hr (T2, n=80), 10 hr (T3, n=17), 12 hr (T4, n=34) and 14 hr fasting on the day of the operation (T5, n=29). RESULTS: Of the patients, 27.5% had a blood glucose level of less than 79 mg/dL at T2; 17.6% at T3; 32.4% at T4; and 17.2% at T5. Mean blood glucose levels were 93.8 mg/dL at T1; 88.4 mg/dL at T2; 91.7 mg/dL at T3; 87.4 mg/dL at T4: and 94.1 mg/dL at T5. Blood glucose was the lowest at T2 (p<.001). CONCLUSION: As 17.6-32.4% of the patients showed the blood glucose level of less than 79 mg/dL at 8-14 hr pre-operative fasting, the authors recommend that surgical patients >60 yr-of-age be observed for hypoglycemia during pre-operative fasting of more than 10 hr and that surgical patients >60 yr-of-age with risks for hypoglycemia be scheduled for operation within 10 hr preoperative fasting.
Aged
;
Aged, 80 and over
;
Blood Glucose/*analysis
;
Body Mass Index
;
*Fasting
;
Female
;
Hemoglobins/analysis
;
Humans
;
Hypoglycemia/blood/prevention & control
;
Male
;
Middle Aged
;
Preoperative Care
;
Risk
;
Serum Albumin/analysis
;
Sex Factors
;
Time Factors
2.Sternal Osteomyelitis Caused by Gordonia bronchialis after Open-Heart Surgery.
Jeong Hyun CHANG ; Misuk JI ; Hyo Lim HONG ; Sang Ho CHOI ; Yang Soo KIM ; Cheol Hyun CHUNG ; Heungsup SUNG ; Mi Na KIM
Infection and Chemotherapy 2014;46(2):110-114
We report the case of a deep sternal wound infection with sternal osteomyelitis caused by Gordonia bronchialis after open-heart surgery. The isolate was identified as a G. bronchialis by 16S rRNA and hsp65 gene sequencing, having initially been misidentified as a Rhodococcus by a commercial phenotypic identification system.
Osteomyelitis*
;
Rhodococcus
;
Wound Infection
3.Improvement Characteristics of Bio-active Materials Coated Fabric on Rat Muscular Mitochondria.
Donghee LEE ; Young Won KIM ; Jung Ha KIM ; Misuk YANG ; Hyemi BAE ; Inja LIM ; Hyoweon BANG ; Kyung Chan GO ; Gwang Wung YANG ; Yong Hwan RHO ; Hyo Suk PARK ; Eun Ho PARK ; Jae Hong KO
The Korean Journal of Physiology and Pharmacology 2015;19(3):283-289
This study surveys the improvement characteristics in old-aged muscular mitochondria by bio-active materials coated fabric (BMCF). To observe the effects, the fabric (10 and 30%) was worn to old-aged rat then the oxygen consumption efficiency and copy numbers of mitochondria, and mRNA expression of apoptosis- and mitophagy-related genes were verified. By wearing the BMCF, the oxidative respiration significantly increased when using the 30% materials coated fabric. The mitochondrial DNA copy number significantly decreased and subsequently recovered in a dose-dependent manner. The respiratory control ratio to mitochondrial DNA copy number showed a dose-dependent increment. As times passed, Bax, caspase 9, PGC-1alpha and beta-actin increased, and Bcl-2 decreased in a dose-dependent manner. However, the BMCF can be seen to have had no effect on Fas receptor. PINK1 expression did not change considerably and was inclined to decrease in control group, but the expression was down-regulated then subsequently increased with the use of the BMCF in a dose-dependent manner. Caspase 3 increased and subsequently decreased in a dose-dependent manner. These results suggest that the BMCF invigorates mitophagy and improves mitochondrial oxidative respiration in skeletal muscle, and in early stage of apoptosis induced by the BMCF is not related to extrinsic death-receptor mediated but mitochondria-mediated signaling pathway.
Actins
;
Animals
;
Antigens, CD95
;
Apoptosis
;
Caspase 3
;
Caspase 9
;
DNA, Mitochondrial
;
Mitochondria*
;
Mitochondrial Degradation
;
Muscle, Skeletal
;
Oxygen Consumption
;
Rats*
;
Respiration
;
RNA, Messenger