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<title>Journal of Intensive Care Medicine current issue</title>
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<prism:coverDisplayDate>May 2008</prism:coverDisplayDate>
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<title>Journal of Intensive Care Medicine</title>
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<item rdf:about="http://jic.sagepub.com/cgi/content/abstract/23/3/151?rss=1">
<title><![CDATA[Analytical Reviews: Antifungal Therapies in the Intensive Care Unit]]></title>
<link>http://jic.sagepub.com/cgi/content/abstract/23/3/151?rss=1</link>
<description><![CDATA[<p>Fungal infections are increasing nationwide, paralleling increases in the number of immunosuppressed hosts. Most of the candida infections seen in the intensive care unit are likely due to iatrogenic factors such as hyperalimentation, catheters, broad-spectrum antibiotics, and postprocedure complications that are prevalent in intensive care unit patients. Delays in appropriate therapy are common and may compromise care. Fortunately, the recognition of several clinical syndromes in the intensive care unit that require specialized treatment can improve outcomes. The issue of antifungal prophylaxis has to be balanced against issues of resistance, and current guidelines are reviewed here for prophylactic use of fluconazole only in selected intensive care unit patients. Finally, several new antifungal agents are available to treat the emerging resistant fungi, with better toxic/therapeutic ratios than in the past. Thus, there are an increasing number of safer and more effective options for treating fungal infections in the intensive care unit.</p>]]></description>
<dc:creator><![CDATA[Chowdhry, R., Marshall, W. L.]]></dc:creator>
<dc:date>2008-05-11</dc:date>
<dc:identifier>info:doi/10.1177/0885066607313000</dc:identifier>
<dc:title><![CDATA[Analytical Reviews: Antifungal Therapies in the Intensive Care Unit]]></dc:title>
<prism:number>3</prism:number>
<prism:volume>23</prism:volume>
<prism:endingPage>158</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>151</prism:startingPage>
<prism:section>Article</prism:section>
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<item rdf:about="http://jic.sagepub.com/cgi/content/abstract/23/3/159?rss=1">
<title><![CDATA[Intensive Care Management of the Patient With Cystic Fibrosis]]></title>
<link>http://jic.sagepub.com/cgi/content/abstract/23/3/159?rss=1</link>
<description><![CDATA[<p>Cystic fibrosis was previously thought to be a disease of childhood. With a better understanding of this condition along with improvements in therapy, patients with cystic fibrosis are now living well into adulthood. The aim of this article is to familiarize the intensive care unit physician with cystic fibrosis care, to discuss complications associated with cystic fibrosis specifically related to the intensive care unit, and to detail the current recommendations for the clinical management of the patient with cystic fibrosis. With advancing disease, the most severely affected organs are the lungs. Obstruction, infection, and inflammation contribute to the decline of pulmonary function, ultimately leading to death. Some patients may be eligible for lung transplantation, but choosing wisely will affect posttransplant survival. Because other organs are affected by the genetic defect and associated treatments, serious complications related to the liver, pancreas, intestines, and kidneys must be considered by the intensivist faced with a patient with cystic fibrosis. As practitioners, the fact that not all patients will survive and help our patients and families gracefully through the end-of-life process should be accepted.</p>]]></description>
<dc:creator><![CDATA[Kremer, T. M., Zwerdling, R. G., Michelson, P. H., O'Sullivan, B. P.]]></dc:creator>
<dc:date>2008-05-11</dc:date>
<dc:identifier>info:doi/10.1177/0885066608315679</dc:identifier>
<dc:title><![CDATA[Intensive Care Management of the Patient With Cystic Fibrosis]]></dc:title>
<prism:number>3</prism:number>
<prism:volume>23</prism:volume>
<prism:endingPage>177</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>159</prism:startingPage>
<prism:section>Article</prism:section>
</item>

<item rdf:about="http://jic.sagepub.com/cgi/content/abstract/23/3/178?rss=1">
<title><![CDATA[Review of A Large Clinical Series: Paroxysmal Atrial Fibrillation in Critically Ill Patients With Sepsis]]></title>
<link>http://jic.sagepub.com/cgi/content/abstract/23/3/178?rss=1</link>
<description><![CDATA[<p>The objective of this retrospective cohort study was to describe the incidence of paroxysmal atrial fibrillation and to determine its risk factors and effect on outcome in critically ill patients with sepsis. The study included 81 patients with sepsis admitted to an intensive care unit. In all, 25 patients (31%) developed paroxysmal atrial fibrillation. Advanced age, history of paroxysmal atrial fibrillation, higher severity of illness at intensive care unit admission, and lower left ventricular ejection fraction were risk factors for paroxysmal atrial fibrillation. Multiple logistic regression analysis showed that paroxysmal atrial fibrillation was independently associated with 28-day mortality (odds ratio = 3.284; 95% confidence interval, 1.126-9.574). The incidence of paroxysmal atrial fibrillation is high in critically ill patients with sepsis. It occurs more frequently in patients with advanced age, history of paroxysmal atrial fibrillation, high severity of illness, and lower left ventricular ejection fraction and is associated with increased mortality.</p>]]></description>
<dc:creator><![CDATA[Salman, S., Bajwa, A., Gajic, O., Afessa, B.]]></dc:creator>
<dc:date>2008-05-11</dc:date>
<dc:identifier>info:doi/10.1177/0885066608315838</dc:identifier>
<dc:title><![CDATA[Review of A Large Clinical Series: Paroxysmal Atrial Fibrillation in Critically Ill Patients With Sepsis]]></dc:title>
<prism:number>3</prism:number>
<prism:volume>23</prism:volume>
<prism:endingPage>183</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>178</prism:startingPage>
<prism:section>Article</prism:section>
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<item rdf:about="http://jic.sagepub.com/cgi/content/abstract/23/3/184?rss=1">
<title><![CDATA[A Prospective Evaluation of Propylene Glycol Clearance and Accumulation During Continuous-Infusion Lorazepam in Critically Ill Patients]]></title>
<link>http://jic.sagepub.com/cgi/content/abstract/23/3/184?rss=1</link>
<description><![CDATA[<p>Propylene glycol is a commonly used diluent in several pharmaceutical preparations, including the sedative lorazepam. Fifty critically ill patients receiving continuous-infusion lorazepam for a minimum of 36 hours were prospectively evaluated to determine the extent of propylene glycol accumulation over time, characterize propylene glycol clearance in the presence of critical illness, and develop a pharmacokinetic model that would predict clearance based on patient-specific clinical, laboratory, and demographic factors. In this cohort, the median lorazepam infusion rate was 2.1 mg/h (0.5-18). Propylene glycol concentration correlated poorly with osmolality, osmol gap, and lactate. In all, 8 patients (16%) had significant propylene glycol accumulation (>25mg/dL). When propylene glycol concentrations were >25 mg/dL, the median lorazepam infusion rate before sample collection was higher, 6.4 (1.9-11.3) versus 2.0 (0.5-7.4) mg/h (<I>P</I> =.0003). A linear first-order model with interoccasion variability on clearance adjusted for total body weight and Acute Physiology and Chronic Health Evaluation II score predicted propylene glycol concentration.</p>]]></description>
<dc:creator><![CDATA[Nelsen, J. L., Haas, C. E., Habtemariam, B., Kaufman, D. C., Partridge, A., Welle, S., Forrest, A.]]></dc:creator>
<dc:date>2008-05-11</dc:date>
<dc:identifier>info:doi/10.1177/0885066608315808</dc:identifier>
<dc:title><![CDATA[A Prospective Evaluation of Propylene Glycol Clearance and Accumulation During Continuous-Infusion Lorazepam in Critically Ill Patients]]></dc:title>
<prism:number>3</prism:number>
<prism:volume>23</prism:volume>
<prism:endingPage>194</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>184</prism:startingPage>
<prism:section>Article</prism:section>
</item>

<item rdf:about="http://jic.sagepub.com/cgi/content/abstract/23/3/195?rss=1">
<title><![CDATA[Intermittent Hemodialysis Versus Continuous Renal Replacement Therapy for Acute Renal Failure in the Intensive Care Unit: An Observational Outcomes Analysis]]></title>
<link>http://jic.sagepub.com/cgi/content/abstract/23/3/195?rss=1</link>
<description><![CDATA[<p><b>Background:</b> Studies have failed to show a survival difference between intermittent hemodialysis (IHD) and continuous renal replacement therapy (CRRT). Comparative cost analyses are limited and fail to control for differences in patient disease severity and comorbid conditions. The authors retrospectively estimated clinical and economic outcomes associated with CRRT and IHD among critically ill patients experiencing acute renal failure (ARF) in 2 tertiary care hospitals in Rochester, Minnesota, between January 1, 2000, and December 12, 2001. <b>Methods:</b> 161 critically ill patients requiring dialysis for ARF were analyzed. Patient demo-graphics, comorbid conditions, ARF etiology, mode of renal replacement therapy (RRT), renal recovery, and survival were abstracted from medical chart. APACHE II scores at dialysis initiation were calculated. Administrative data tracked length of stay (LOS) and direct medical costs from initiation of RRT to death or intensive care unit (ICU) and hospital discharge. Multivariate modeling was used to adjust outcomes for baseline differences. <b>Results:</b> 84 (52%) of the patients received CRRT and 77 (48%) received IHD. CRRT-treated patients were younger (58 vs 65 years), less likely male (58% vs 77%), had higher APACHE II scores (32 vs 27) with a higher incidence of sepsis (46% vs 30%) and respiratory disease (56% vs 39%), and were less likely to have chronic renal insufficiency (32% vs 49%). With adjustment for differences in baseline patient characteristics, the RRT method did not affect the likelihood of renal recovery, in-hospital survival, or survival during follow-up. Mean adjusted ICU LOS was 9.5 days shorter for IHD-treated than CRRT-treated patients (<I>P</I> &lt; .001), and the adjusted mean difference in hospital and total costs associated with ICU stay was $56 564 and $60 827, in favor of IHD (<I>P</I> &lt; .001). Mean adjusted total costs through hospital discharge were $93 611 and $140 733 among IHD-treated and CRRT-treated patients, respectively (<I>P</I> &lt; .001). <b>Conclusions:</b> This observational study suggests that costs may significantly differ by mode of RRT despite similar severity-adjusted patient outcomes. Future prospective comparisons of renal replacement modalities will need to include both clinical and economic outcomes.</p>]]></description>
<dc:creator><![CDATA[Abdul Rauf, A., Hall Long, K., Gajic, O., Anderson, S. S., Swaminathan, L., Albright, R. C.]]></dc:creator>
<dc:date>2008-05-11</dc:date>
<dc:identifier>info:doi/10.1177/0885066608315743</dc:identifier>
<dc:title><![CDATA[Intermittent Hemodialysis Versus Continuous Renal Replacement Therapy for Acute Renal Failure in the Intensive Care Unit: An Observational Outcomes Analysis]]></dc:title>
<prism:number>3</prism:number>
<prism:volume>23</prism:volume>
<prism:endingPage>203</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>195</prism:startingPage>
<prism:section>Article</prism:section>
</item>

<item rdf:about="http://jic.sagepub.com/cgi/content/abstract/23/3/204?rss=1">
<title><![CDATA[Paradoxical Air Embolism Successfully Treated With Hyperbaric Oxygen]]></title>
<link>http://jic.sagepub.com/cgi/content/abstract/23/3/204?rss=1</link>
<description><![CDATA[<p>The use of the central venous catheter may be complicated by air embolism when central venous pressure is subatmospheric and the catheter is open to the surrounding air. Paradoxical air embolus occurs when the gas bubbles are able to traverse a right to left shunt, gaining access to the systemic arterial circulation causing ischemic symptoms in end organs. In this article, a case of a patient with an unknown patent foramen ovale through which air entered the arterial circulation resulting in obtundation and stroke after inadvertent manipulation of a Hickman catheter is presented. The physiology, clinical manifestations, and management strategies are also discussed.</p>]]></description>
<dc:creator><![CDATA[Scruggs, J. E., Joffe, A., Wood, K. E.]]></dc:creator>
<dc:date>2008-05-11</dc:date>
<dc:identifier>info:doi/10.1177/0885066607312865</dc:identifier>
<dc:title><![CDATA[Paradoxical Air Embolism Successfully Treated With Hyperbaric Oxygen]]></dc:title>
<prism:number>3</prism:number>
<prism:volume>23</prism:volume>
<prism:endingPage>209</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>204</prism:startingPage>
<prism:section>Article</prism:section>
</item>

<item rdf:about="http://jic.sagepub.com/cgi/content/abstract/23/3/210?rss=1">
<title><![CDATA[Perioperative Management of a 7-Year-Old Child With Brugada Syndrome]]></title>
<link>http://jic.sagepub.com/cgi/content/abstract/23/3/210?rss=1</link>
<description><![CDATA[<p>Brugada syndrome results from abnormalities in the myocardial transmembrane conduction of sodium, resulting in the characteristic electrocardiographic changes of ST segment elevation in the precordial leads and incomplete right bundle branch block in an otherwise structurally normal heart. Affected patients are frequently asymptomatic until their presentation with potentially lethal arrhythmias including ventricular fibrillation. The youngest reported patient with Brugada syndrome to undergo anesthetic management is presented in this article; the pathophysiology of the syndrome is reviewed, and its perioperative implications are discussed.</p>]]></description>
<dc:creator><![CDATA[Baty, L., Hollister, J., Tobias, J. D.]]></dc:creator>
<dc:date>2008-05-11</dc:date>
<dc:identifier>info:doi/10.1177/0885066608315823</dc:identifier>
<dc:title><![CDATA[Perioperative Management of a 7-Year-Old Child With Brugada Syndrome]]></dc:title>
<prism:number>3</prism:number>
<prism:volume>23</prism:volume>
<prism:endingPage>214</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>210</prism:startingPage>
<prism:section>Article</prism:section>
</item>

<item rdf:about="http://jic.sagepub.com/cgi/reprint/23/3/215?rss=1">
<title><![CDATA[Book Review: Heart Disease Diagnosis and Therapy. M. Gabriel Khan. Humana Press. 2005. $99.50 Humana Press, Totowa, New Jersey]]></title>
<link>http://jic.sagepub.com/cgi/reprint/23/3/215?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Ferullo, J. A.]]></dc:creator>
<dc:date>2008-05-11</dc:date>
<dc:identifier>info:doi/10.1177/0885066608315799</dc:identifier>
<dc:title><![CDATA[Book Review: Heart Disease Diagnosis and Therapy. M. Gabriel Khan. Humana Press. 2005. $99.50 Humana Press, Totowa, New Jersey]]></dc:title>
<prism:number>3</prism:number>
<prism:volume>23</prism:volume>
<prism:endingPage>215</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>215</prism:startingPage>
<prism:section>Article</prism:section>
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