2013年2月24日 星期日


A Randomized Controlled Trial of Nebulized Gentamicin in NonCystic Fibrosis Bronchiectasis

Authors: Maeve P. Murray, John R. W. Govan, Catherine J. Doherty, et al.
Journal: Am J Respir Crit Care Med Vol 183. pp 491499, 2011

報告者:孫文娟  呼吸治療師
指導者:鄭瑞駿  臨床組長
報告日期:2012220


Rationale: Bronchiectasis is a chronic debilitating disease with few evidence-based long-term treatments.
Objectives: A randomized controlled trial assessing the efficacy of nebulized gentamicin therapy over 1 year in patients with non–cystic fibrosis bronchiectasis.
Methods: Sixty-five patients were randomized to either twice-daily nebulized gentamicin, 80 mg, or nebulized 0.9% saline, for 12 months. All were reviewed at three-monthly intervals during treatment and at 3 months’ follow-up. Measurements and Main Results: At each review the following were assessed: quantitative and qualitative sputum bacteriology; sputum purulence and 24-hour volume; FEV1, FVC, and forced expiratory flow, mid expiratory phase; exercise capacity; Leicester Cough Questionnaire and St. George’s Respiratory Questionnaire; and exacerbation frequency. Fifty-seven patients completed the study. At the end of 12 months’ treatment, compared with the saline group, in the gentamicin group there was reduced sputum bacterial density with 30.8% eradication in those infected with Pseudomonas aeruginosa and 92.8% eradication in those infected with other pathogens; less sputum purulence (8.7% vs. 38.5%; P<0.0001); greater exercise capacity (510 [350–690]m vs. 415 [267.5–530]m; P=0.03); and fewer exacerbations (0 [0–1] vs. 1.5 [1–2]; P<0.0001) with increased time to first exacerbation (120 [87–161.5] d vs. 61.5 [20.7–122.7] d; P=0.02). The gentamicin group had greater improvements in Leicester Cough Questionnaire (81.4% vs. 20%; P<0.01) and St. George’s Respiratory Questionnaire (87.5%vs. 19.2%; P<0.004) score. No differences were seen in 24-hour sputum volume, FEV1, FVC, or forced expiratory flow, mid expiratory phase. No P. aeruginosa isolates developed resistance to gentamicin. At follow-up, all outcome measures were similar to baseline.
Conclusions: Regular, long-term nebulized gentamicin is of significant benefit in non–cystic fibrosis bronchiectasis but treatment needs to be continuous for its ongoing efficacy.

2013年1月1日 星期二

AUTOMATED OXYGEN FLOW TITRATION TO MAINTAIN CONSTANT OXYGENATION

報告者:陳敏雄 呼吸治療師
報告日期:102.01.02

作者:Lellouche F, L'her E.
出處: 2012 Aug;57(8):1254-62.
http://rc.rcjournal.com/content/57/8/1254.full.pdf+html

Abstract

BACKGROUND:

One century after the introduction of the oxygen flow meter into clinical practice, we have developed a device, FreeO(2), that automatically titrates the oxygen flow delivered to spontaneously breathing patients, with the aim of maintaining a stable S(pO(2)). We evaluated this system in healthy subjects during induced hypoxemia.

METHODS:

Hypoxemia was induced in 10 healthy subjects while breathing a gas mixture of variable FIO(2 (air + nitrogen). Each subject performed 3 hypoxemic challenges with the addition, in a random order, of either: air with constant flow (1.5 L/min); oxygen with constant flow (1.5 L/min); or automatic oxygen flow titration. Subjects were blinded to the intervention. Oxygen flow, SpO2, end-tidal CO(2), respiratory rate, and heart rate were recorded every second. The primary outcome was the time with S(pO(2)) between 92% and 96%.

RESULTS:

The SpO2 target (92-96%) was achieved a median of 26.0%, 36.8%, and 66.5% (P < .001) of the time with air, constant oxygen, and automated oxygen titration, respectively. Severe oxygen desaturations (SpO2 < 88%) were respectively observed at a median of 33.7%, 12.7%, and 0.4% of the time (P < .001). Hyperoxia was present a median of 4.1%, 39.1%, and 14.5% of the time (P < .001). Tachycardia was present with air and with constant oxygen flow, but not while using automated oxygen titration. These results were obtained with a mean and maximal oxygen flow of 1.3 L/min and 7.6 L/min with the automated titration.

CONCLUSIONS:

In this model of induced hypoxemia, the FreeO2 system that automatically titrates the oxygen flow was more efficient at maintaining the SpO2 target, while ensuring a statistically significant reduction in the rates of severe hypoxemia and hyperoxia, in comparison with air or constant oxygen flow. These beneficial results were obtained with less oxygen, in comparison to a constant oxygen flow.



 
Resource from: 2012 Aug;57(8):1254-62.
 

2012年12月2日 星期日

Sequential Organ Failure Assessment (SOFA) score



Model for end-stage liver disease score(MELD)

MELD(Model for end-stage liver disease) score   
計算公式:
 MELD Score = (0.957 * ln(Serum Cr) + 0.378 * ln(Serum Bilirubin) + 1.120 * ln(INR) + 0.643 ) * 10 (if hemodialysis, value for Creatinine is automatically set to 4.0)
the 3 month mortality is: [6]
40 or more — 71.3% mortality
30–39 — 52.6% mortality
20–29 — 19.6% mortality
10–19 — 6.0% mortality
<9 — 1.9% mortality
Source from http://en.wikipedia.org/wiki/Model_for_End-Stage_Liver_Disease
Pre-operative usage of molecular adsorbent re-circulating system (MARS)

MARS(Molecular Adsorbent Recycling System)
是一種新型人工肝臟支持系統目的為延長等待時間增加急性肝衰竭患者接受肝臟移植手術的機會該系統將血液引流到體外,血液的毒素經由特殊的透析膜,被另一側循環的白蛋白溶液吸附帶走,經過透析、活性碳吸附、樹脂吸附,乾淨的白蛋白溶液再循環重複使用。其毒素移除效果好,不良反應少。處理後的乾淨血液回輸患者體內,每次治療約需68小時,一般治療期間需每天或每2天洗1次,不過費用高昂,每洗1次約需1520萬元,健保並未給付。
CTP(Child-Turcotte-Pugh)

Measure1 point2 points3 points
Total bilirubin, μmol/l (mg/dl)<34 (<2)34-50 (2-3)>50 (>3)
Serum albumin, g/l>3528-35<28
PT INR<1.71.71-2.30> 2.30
AscitesNoneMildModerate to Severe
Hepatic encephalopathyNoneGrade I-II (or suppressed with medication)Grade III-IV (or refractory)

PointsClassOne year survivalTwo year survival
5-6A100%85%
7-9B81%57%
10-15C45%35%

source from: http://en.wikipedia.org/wiki/Child-Pugh_score


Cuff-leak test for the diagnosis of upper airway obstruction in adults: a systematic review and meta-analysis

Maria Elena Ochoa, Maria del Carmen Marı´n, Fernando Frutos-Vivar, Federico Gordo, Jaime Latour-Pe´rez, Enrique Calvo, Andres Esteban   
Intensive Care Med (2009) 35(7):1171-9

報告者:廖瑞琪 101.12.19

Abstract
Purpose:
To evaluate, in adults, the diagnostic accuracy of the cuff-leak test for the diagnosis of upper airway obstruction secondary to laryngeal edema and for reintubation secondary to upper airway obstruction.

Methods:
Systematic review without language restrictions based on electronic databases and manual review of the literature up to December 2008. When appropriate, a random-effects meta-analysis and meta-regression (Moses’ method) were performed.

Results:
Upper airway obstruction was the outcome in nine studies with an overall incidence of 6.9%. There was significant heterogeneity among studies. The pooled sensitivity was 0.56 (95% confidence interval: 0.48–0.63), the specificity was 0.92 (95% CI: 0.90–0.93), the positive likelihood ratio was 5.90 (95% CI: 4.00–8.69), the negative likelihood ratio was 0.48 (95% CI: 0.33–0.72), and the diagnostic odds ratio was 18.78 (95% CI:7.36–47.92). The area under the curve of the summary receiver-operator characteristic (SROC) was 0.92 (95% CI: 0.89–0.94). Only three studies have evaluated the accuracy of the cuff-leak test for reintubation secondary to upper airway obstruction. Overall incidence was 7%. The pooled sensitivity was 0.63 (95% CI: 0.38–0.84), the specificity was 0.86 (95% CI: 0.81–0.90), the positive likelihood ratio was 4.04 (95% CI:2.21–7.40), the negative likelihood ratio was 0.46 (95% CI: 0.26–0.82), and the diagnostic odds ratio was 10.37 (95% CI: 3.70–29.13).

Conclusions:
A positive cuff-leak test (absence of leak) should alert the clinician of a high risk of upper airway obstruction.