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34


SIMULATION TRAINING IMPROVES RESIDENTS KNOWLEDGE AND ADHERENCE TO THE SURVIVING SEPSIS GUIDELINES [Meeting Abstract]

Coan, Amy; Desai, Anish; Gadhvi, Sonya; Milligan, Zach; Kutzin, Jared; Spiegler, Peter; Chawla, Shalinee; Mathew, Joseph
ISI:000374778401212
ISSN: 0090-3493
CID: 3502322

The Case | Elevated lactate and osmolar gap after levothyroxine overdose [Case Report]

Rothberger, Gary D; Desai, Anish K; Sharif, Sairah; Chawla, Shalinee A; Shirazian, Shayan
PMID: 26230209
ISSN: 1523-1755
CID: 3462092

Current controversies in the support of sepsis

Chawla, Shalinee; DeMuro, Jonas P
PURPOSE OF REVIEW/OBJECTIVE:Sepsis has a high morbidity, with a mortality rate of over 50% in the septic shock patient. This review provides a comprehensive summary of the latest Surviving Sepsis Campaign and the recent evidence since its publication. The guidelines reflect literature from the past 5 years to optimize outcomes in patients with severe sepsis and septic shock. RECENT FINDINGS/RESULTS:The most relevant changes in the latest Surviving Sepsis Campaign include the use of a protocolized resuscitation with specific physiologic targets, preference of crystalloids for volume resuscitation, preferential use of norepinephrine as the initial vasopressor, addition of lactate and its clearance as a marker of tissue hypoperfusion, reduced emphasis on corticosteroids, and removal of activated protein C therapy. Since these latest guidelines, there have been many trials published to address the various measures that are advocated. We review the recent data on fluid resuscitation, targets of resuscitation, vasopressors, and trials of protocolized care versus usual care. SUMMARY/CONCLUSIONS:Severe sepsis remains a significant cause of morbidity and mortality in hospitalized patients. The International Surviving Sepsis Guidelines provide a framework for early recognition and treatment of this condition, with the goal of an improved outcome and mortality in severe sepsis. The recent evidence suggests that early identification, adequate volume resuscitation, and assessment of adequate circulation may be the key elements to decrease morbidity from severe sepsis and septic shock.
PMID: 25340379
ISSN: 1531-7072
CID: 3462122

"Where Did That Thing Come From?!": Case Report of a Rapidly Migrating Right Atrial Thrombus [Meeting Abstract]

Patel, Jay; Nair, Girish B.; Klek, Stanislaw; Louka, Boshra; Chong, Melanie; D'Anca, Michael; Liu, Jeffrey; Chawla, Shalinee
ISI:000326864001104
ISSN: 0012-3692
CID: 3388332

An Unusual Presentation of Squamous Cell Carcinoma of Lung in an Immunocompromised Patient Mimicking Pulmonary Artery Embolism [Meeting Abstract]

Pang, Joyce; Nair, Girish B.; Ilowite, Jonathan; Hoffman, Jason; Chawla, Shalinee
ISI:000326864002006
ISSN: 0012-3692
CID: 3462102

Ergonomics in bronchoscopy: is there a need for better design or a change in the work environment? [Editorial]

Nair, Girish B; Chawla, Shalinee; Ilowite, Jonathan S
PMID: 22283569
ISSN: 1747-6356
CID: 3462032

Fulminant myocarditis associated with novel H1N1 influenza A [Case Report]

Khouzam, Rami N; Parizianu, Constantin; Hafiz, Abdul Moiz; Chawla, Shalinee; Schwartz, Richard
Myocarditis secondary to H1N1 influenza has been described in children, but only very rarely in adults. We describe a 36-year-old man with no significant medical history who presented with flu-like symptoms of 3-week duration. When he sought medical attention, he was already manifesting heart failure secondary to fulminant myocarditis, along with multiorgan failure. Despite aggressive management, including circulatory support with a catheter-based mechanical cardiac assist device (Impella 2.5 Cardiac Assist Device, Abiomed, Danvers, MA) as a bridge to cardiac transplant, and aggressive antiviral and antibacterial therapy, the patient died of cardiac arrest. An H1N1 polymerase chain reaction postmortem assay produced positive results, and a diagnosis of fulminant viral myocarditis and multiorgan system failure was established.
PMID: 21411147
ISSN: 1527-3288
CID: 3462012

Celiac disease in children, adolescents, and young adults with autoimmune thyroid disease

Sattar, Nadia; Lazare, Farrah; Kacer, Martina; Aguayo-Figueroa, Lourdes; Desikan, Vardhini; Garcia, Mireya; Lane, Andrew; Chawla, Anupama; Wilson, Thomas
OBJECTIVE:To determine the prevalence of antibodies associated with celiac disease and biopsy-proven celiac disease in children with autoimmune thyroid disease. STUDY DESIGN/METHODS:A total of 302 patients with positive anti-thyroid antibodies were prospectively studied. Total immunoglobulin A (IgA) and tissue transglutaminase-IgA (tTG-IgA) levels were obtained. Those with a positive tTG-IgA titer were offered biopsy for definitive diagnosis of celiac disease. RESULTS:A total of 4.6% of subjects with autoimmune thyroid disease had positive tTG-IgA titers. The prevalence of biopsy-confirmed celiac disease was 2.3%. Our population was enriched with patients with type 1 diabetes mellitus (4.3%) and Down syndrome (3.4%). Excluding individuals with these co-morbidities, the prevalence of celiac disease in autoimmune thyroid disease is 1.3%, similar to that of the general population. The positive predictive value of biopsy-proven celiac disease in patients with autoimmune thyroid disease and positive tTG-IgA titer was 54%. CONCLUSION/CONCLUSIONS:The increase in prevalence of celiac disease in autoimmune thyroid disease in our study was largely caused by enrichment with co-morbidities. Without comorbidities or symptoms, screening for celiac disease may not be justified in this population. The specificity of tTG-IgA titer for the diagnosis of celiac disease was decreased in patients with autoimmune thyroid disease compared with the general population.
PMID: 20961564
ISSN: 1097-6833
CID: 3537982

New Model Leading to Preterm Delivery: The Role of Exposure to Environmental Toxins [Meeting Abstract]

Kiefer, D; Keeler, S; Cremer, M; Chawla, K; Lerner, V; Hanna, N
ISI:000275558600370
ISSN: 1933-7191
CID: 110131

Does Oxygen Tension Alter Cytokine Expression in Human Placental Explants? [Meeting Abstract]

Kiefer, D; Lerner, V; Chawla, K; Cremer, M; Muscat, J; Hanna, N
ISI:000275558601367
ISSN: 1933-7191
CID: 110133