scispace - formally typeset
Search or ask a question

Showing papers by "Lena M. Napolitano published in 2012"


Journal ArticleDOI
TL;DR: In this paper, the authors discuss epidemiology, risk factors, diagnosis, treatment, and prevention of postoperative pulmonary complications in surgical patients, particularly after abdominal and thoracic surgery, pneumonia and atelectasis being the most common.

77 citations


Journal ArticleDOI
TL;DR: The findings from this large prospective observational study that characterized patients with cSSTIs from diverse US inpatient populations provide useful information on the current epidemiology, clinical management practices and outcomes of this common infection.
Abstract: Background Complicated skin and soft tissue infections (cSSTIs) occur frequently, but limited data do not allow any consensus on an optimal treatment strategy. We designed this prospective, multicenter, observational study to to explore the current epidemiology, treatment, and resulting clinical outcomes of cSSTIs to help develop strategies to potentially improve outcomes.

51 citations


Journal ArticleDOI
TL;DR: Empiriology, risk factors, diagnosis, treatment, and prevention of complications in critically ill patients, including ventilator-associated pneumonia, are discussed.

36 citations


Journal ArticleDOI
TL;DR: To investigate oseltamivir and oselTAMivir carboxylate pharmacokinetics in critically ill patients who were receiving continuous venovenous hemodialysis and extracorporeal membrane oxygenation.
Abstract: tudy Objective To investigate oseltamivir and oseltamivir carboxylate pharmacokinetics in critically ill patients who were receiving continuous venovenous hemodialysis (CVVHD) and/or extracorporeal membrane oxygenation (ECMO). Design Prospective, open-label, pharmacokinetic study. Setting Intensive care units of an academic medical center. Patients Thirteen critically ill patients aged 13 years or older with suspected or confirmed H1N1 influenza who had a prescription for oseltamivir and were concurrently receiving CVVHD and/or ECMO between October 2009 and January 2010. Intervention Oseltamivir 150 mg was administered nasogastrically or nasoenterically every 12 hours. Blood samples were collected at baseline and at 1, 2, 4, 6, 8, 10, and 12 hours after administration of the fourth oseltamivir dose or subsequent doses. In patients receiving CVVHD, effluent also was collected at the same time points. Urine was collected throughout the 12-hour dosing interval. Measurements and Main Results Eight patients received CVVHD only, four patients received both CVVHD and ECMO, and one patient received ECMO only. Pharmacokinetic parameters for the patient who received only ECMO were not reported. The median maximum plasma concentration and area under the plasma concentration–time curve for the 12-hour dosing interval (AUC0–12) for the remaining 12 patients were 83.4 ng/ml and 216 ng•hour/ml, respectively, for oseltamivir and 2000 ng/ml and 21,500 ng•hour/ml, respectively, for oseltamivir carboxylate. Mean clearance due to CVVHD was 33.8 ml/minute for oseltamivir and 50.2 ml/minute for oseltamivir carboxylate. For patients who received ECMO, no substantial differences between pre- and post-ECMO oxygenator plasma concentrations were found for oseltamivir or oseltamivir carboxylate. Conclusion Although the optimal pharmacokinetic-pharmacodynamic targets for oseltamivir carboxylate remain unclear, in the patients receiving CVVHD with or without ECMO, a regimen of oseltamivir 150 mg every 12 hours yielded a median oseltamivir carboxylate AUC0–12 considerably higher than would be expected in non–critically ill patients receiving the same dosage regimen.

34 citations


Journal ArticleDOI
TL;DR: Heidi L. Frankel, MD, Karyn L.Frankel, MPH, Raul Coimbra,MD, PhD, Martin A. Jurkovich, Md, Ernest E. Moore, Jr., MD, John A. Morris, Jr., and J. Wayne Meredith are among the authors of this book.
Abstract: Heidi L. Frankel, MD, Karyn L. Butler, MD, Joseph Cuschieri, MD, Randall S. Friese, MD, Toan Huynh, MD, Alicia M. Mohr, MD, Miren A. Schinco, MD, Lena M. Napolitano, MD, L.D. Britt, MD, MPH, Raul Coimbra, MD, PhD, Martin A. Croce, MD, James W. Davis, MD, Gregory J. Jurkovich, MD, Ernest E. Moore, MD, John A. Morris, Jr., MD, Andrew B. Peitzman, MD, Basil A. Pruitt, MD, Grace S. Rozycki, MD, MBA, Thomas M. Scalea, MD, and J. Wayne Meredith, MD, Baltimore, Maryland

32 citations


Journal ArticleDOI
TL;DR: This study confirmed that the use of an MRI template is an accurate tool in determining whether an obese patient can fit through the MRI bore and be accommodated in the MRI scanner.
Abstract: Excessive obesity poses a significant limitation to radiographic magnetic resonance imaging (MRI), particularly related to aperture or bore diameter due to the patient’s girth. Determination of whether a patient will fit into the bore of the MRI scanner is currently accomplished using patient height, weight, and MRI technician experience. These simple methods have proven unreliable. We sought to develop a device and method which could accurately determine whether a patient would fit into the MRI scanner. We developed an MRI template prototype which was tested against the standard radiology methods in a pilot study (n = 6). We then performed a prospective validation study in adult human volunteers (n = 100) to assess the accuracy of the MRI template. We collected height, weight, shoulder and pelvis girth/diameter for each study participant to evaluate the body dimension measurements that would assist in determination of whether a patient would fit into the MRI scanner. Using the MRI template, we determined that 11 of the 100 study participants would not fit in the MRI scanner and 10 were confirmed to not fit into the MRI aperture [positive predictive value (PPV) 0.91 (0.58–0.99); negative predictive value (NPV) 1.00 (0.95–1.00), sensitivity 1.00 (0.69–1.00), specificity 0.99 (0.93–0.99), likelihood ratio positive test 90 (12.81–632), likelihood ratio negative test 0, accuracy 99%]. In comparison, the body measurement method did not perform as well [PPV 0.66 (0.34–0.90), NPV 0.97 (0.92–0.99), sensitivity 0.80 (0.44–0.97), specificity 0.95 (0.89–0.98), likelihood ratio positive test 17.97 (6.56–49.2), likelihood ratio negative test 0.209 (0.06–0.72), accuracy 94%]. This study confirmed that the use of an MRI template is an accurate tool in determining whether an obese patient can fit through the MRI bore and be accommodated in the MRI scanner.

11 citations


Journal ArticleDOI
TL;DR: Prehospital use of amiodarone may independently increase the risk for ARDS in patients who have at least 1 predisposing condition for ALI.

10 citations


Journal ArticleDOI
TL;DR: 1. Igonin AA, Protsenko DN, Galstyan GM, et al: C1-esterase inhibitor infusion increases survival rates for patients with sepsis and in the vascular leak syndrome induced by high doses of interleukin-2 therapy.
Abstract: 1. Igonin AA, Protsenko DN, Galstyan GM, et al: C1-esterase inhibitor infusion increases survival rates for patients with sepsis. Crit Care Med 2012; 40:770–777 2. Hack CE, Ogilvie AC, Eisele B, et al: C1inhibitor substitution therapy in septic shock and in the vascular leak syndrome induced by high doses of interleukin-2. Intensive Care Med 1993; 19:S19–S28 3. Hack CE, Ogilvie AC, Eisele B, et al: Initial studies on the administration of C1-esterase inhibitor to patients with septic shock or with a vascular leak syndrome induced by interleukin-2 therapy. Prog Clin Biol Res 1994; 388:335–357 4. Caliezi C, Zeerleder S, Redondo M, et al: C1-inhibitor in patients with severe sepsis and septic shock: Beneficial effect on renal dysfunction. Crit Care Med 2002; 30: 1722–1728 5. Horstick G, Berg O, Heimann A, et al: Application of C1-esterase inhibitor during reperfusion of ischemic myocardium: Doserelated beneficial versus detrimental effects. Circulation 2001; 104:3125–3131 6. Oikonomopoulou K, Ricklin D, Ward PA, et al: Interactions between coagulation and complement-their role in inflammation. Semin Immunopathol 2012; 34:151–165. 7. Younger JG, Bracho DO, Chung-Esaki HM, et al: Complement activation in emergency department patients with severe sepsis. Acad Emerg Med 2010; 17:353–359 8. Hack CE, Nuijens JH, Felt-Bersma RJ, et al: Elevated plasma levels of the anaphylatoxins C3a and C4a are associated with a fatal outcome in sepsis. Am J Med 1989; 86:20–26 9. Bosmann M, Ward PA: Role of c3, c5 and anaphylatoxin receptors in acute lung injury and in sepsis. Adv Exp Med Biol 2012; 946: 147–159 10. Oehmcke S, Herwald H: Contact system activation in severe infectious diseases. J Mol Med (Berl) 2010; 88:121–126 11. Madeddu P, Emanueli C, El-Dahr S: Mechanisms of disease: The tissue kallikrein-kinin system in hypertension and vascular remodeling. Nat Clin Pract Nephrol 2007; 3:208–221 12. Davis AE 3rd: The pathophysiology of hereditary angioedema. Clin Immunol 2005; 114: 3–9 13. Kaplan AP: Enzymatic pathways in the pathogenesis of hereditary angioedema: The role of C1 inhibitor therapy. J Allergy Clin Immunol 2010; 126:918–925 14. Davis AE 3rd, Lu F, Mejia P: C1 inhibitor, a multi-functional serine protease inhibitor. Thromb Haemost 2010; 104:886–893 15. Kalter ES, Daha MR, ten Cate JW, et al: Activation and inhibition of Hageman factordependent pathways and the complement system in uncomplicated bacteremia or bacterial shock. J Infect Dis 1985; 151:1019–1027 16. Nuijens JH, Eerenberg-Belmer AJ, Huijbregts CC, et al: Proteolytic inactivation of plasma C1inhibitor in sepsis. J Clin Invest 1989; 84:443–450 17. Leid RW, Ballieux BE, van der Heijden I, et al: Cleavage and inactivation of human C1 inhibitor by the human leukocyte proteinase, proteinase 3. Eur J Immunol 1993; 23: 2939–2944 18. Zuraw BL: Clinical practice. Hereditary angioedema. N Engl J Med 2008; 359: 1027–1036 19. Bowen T, Cicardi M, Farkas H, et al: 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema. Allergy Asthma Clin Immunol 2010; 6:24 20. Zuraw BL: HAE therapies: Past present and future. Allergy Asthma Clin Immunol 2010; 6:23 21. Schmidt W, Stenzel K, Gebhard MM, et al: C1-esterase inhibitor and its effects on endotoxin-induced leukocyte adherence and plasma extravasation in postcapillary venules. Surgery 1999; 125:280–287 22. Wagner E, Frank MM: Therapeutic potential of complement modulation. Nat Rev Drug Discov 2010; 9:43–56

10 citations


Journal ArticleDOI
TL;DR: A simple method for guidewire exchange of the femoral venous ECMO cannula to a working catheter for intravascular ultrasound (IVUS) IVC filter placement is developed.
Abstract: Venous thromboembolism (VTE), particularly thrombi in the inferior vena cava (IVC) and pulmonary embolism, can occur after successful extracorporeal membrane oxygenation (ECMO) and can be associated with adverse outcomes including death. VTE is related to the presence of a venous cannula and in some cases inadequate anticoagulation caused by clinical bleeding. We have developed a simple method for guidewire exchange of the femoral venous ECMO cannula to a working catheter for intravascular ultrasound (IVUS) IVC filter placement, and describe the specific methodology.

6 citations