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91 citation(s) found for "Cartin‐Ceba, Rodrigo".

Primary Antiphospholipid Syndrome–Associated Diffuse Alveolar Hemorrhage
Cartin‐Ceba, Rodrigo , Peikert, Tobias, Ashrani, Aneel A. , Keogh, Karina A., Wylam, Mark E. , Ytterberg, Steven R. , Specks, Ulrich

Mayo Clinic

Arthritis Care & Research | August 27, 2013 | Volume: 66 | Issue: 2 | Pages: 301-310

10.1002/acr.22109 | PMID 23983016 Get It

Objective Diffuse alveolar hemorrhage (DAH) is an uncommon complication of primary antiphospholipid syndrome (APS). We aimed to describe the clinical characteristics, treatment, and outcomes of primary APS–associated DAH in a single center. Methods We conducted a retrospective review of all adults with primary APS–associated DAH evaluated at Mayo Clinic over a 15‐year period. DAH was defined as bilateral pulmonary infiltrates and bronchoalveolar lavage (BAL) fluid documenting progressively bloody returns and/or the presence of >20% hemosiderin‐laden macrophages. Patients with other causes of DAH were excluded. Results Eighteen patients were identified (median age 43 years). Capillaritis was present in surgical lung biopsy samples of 3 patients. BAL differential cell counts revealed predominantly neutrophils. All patients were treated initially with glucocorticoids. Cyclophosphamide (CYC) was used in 8 patients; complete remission was achieved in 3 patients treated with CYC alone and in 1 patient receiving combination therapy with rituximab (RTX). RTX was used in 9 patients; 2 patients achieved remission with RTX alone, whereas 3 patients required combination therapy with CYC or mycophenolate mofetil (MMF). No patient achieved complete remission while receiving single therapy with MMF, azathioprine, or plasma exchange. Intravenous gamma globulin therapy was administered in 5 patients; no patient achieved control of the disease. Six patients died, all because of complications related to uncontrolled DAH or its therapy. Conclusion We present the largest case series of primary APS–associated DAH reported in the literature. DAH carries a very poor prognosis and therapeutic options are limited. Immunosuppression with either CYC or RTX is associated with the highest likelihood of remission induction and should be considered early.
Validation of Computerized Automatic Calculation of the Sequential Organ Failure Assessment Score
Harrison, Andrew M. , Yadav, Hemang , Pickering, Brian W. , Cartin‐Ceba, Rodrigo , Herasevich, Vitaly , Harrison, Andrew Marc , Herasevich, Vitaly

Mayo Clinic

Critical Care Research and Practice | July 9, 2013 | Volume: 2013 | Issue: No issue available | Pages: 1-8

10.1155/2013/975672 | PMID 23936639 Get It

Purpose. To validate the use of a computer program for the automatic calculation of the sequential organ failure assessment (SOFA) score, as compared to the gold standard of manual chart review.Materials and Methods. Adult admissions (age > 18 years) to the medical ICU with a length of stay greater than 24 hours were studied in the setting of an academic tertiary referral center. A retrospective cross-sectional analysis was performed using a derivation cohort to compare automatic calculation of the SOFA score to the gold standard of manual chart review. After critical appraisal of sources of disagreement, another analysis was performed using an independent validation cohort. Then, a prospective observational analysis was performed using an implementation of this computer program in AWARE Dashboard, which is an existing real-time patient EMR system for use in the ICU.Results. Good agreement between the manual and automatic SOFA calculations was observed for both the derivation (N=94) and validation (N=268) cohorts: 0.02 ± 2.33 and 0.29 ± 1.75 points, respectively. These results were validated in AWARE (N=60).Conclusion. This EMR-based automatic tool accurately calculates SOFA scores and can facilitate ICU decisions without the need for manual data collection. This tool can also be employed in a real-time electronic environment.
Contemporary Ventilator Management in Patients With and at Risk of ALI/ARDS
Chang, Steven Y., Dabbagh, Ousama, Gajic, O, Patrawalla, Amee , Elie, Marie‐Carmelle , Talmor, Daniel , Malhotra, Atul , Adesanya, Adebola, Anderson, Harry L, Blum, James M. , Park, Pauline K. , Gong, Michelle N. , (USCIITG-LIPS), on behalf of the United States Critical Illness and Injury Trials Group: Lung Injury Prevention Study Investigators, (USCIITG-LIPS), the United States Critical Illness and Injury Trials Group: Lung Injury Prevention Study Investigators, Talmor, Daniel S, Bender, S Patrick, Garcia, Mauricio, Hou, Peter C, Barry, Jonathan M, Shempp, Iam, Malhotra, Atul, Frendl, Gyorgy, Ahmed, Adil, Gajic, Ognjen, Malinchoc, Michael, Kor, Daryl J, Afessa, Bekele, Cartin-Ceba, Rodrigo, Gong, Michelle Ng, Gentile, Nina T, Stevenson, Karen, Freeman, Brent, Srinivasan, Sujatha, Sevransky, Jonathan, Chang, Steven Y, Patrawalla, Amee, Elie, Carmelle, Hamdani, Irram, Seiden, Jason, Douglas, Ivor, Mikkelsen, Mark, Christie, Jason D, Gaieski, David F, Lanken, Paul, Meyer, Nuala, Sha, Chirag, Park, Pauline K, Harris, Julie, Napolitano, Lena, Raghavendran, Krishnan, Hyzy, Robert C, Blum, James, Watkins, Timothy R, Deem, Steven, Treggiari, Miriam, Adesanya, Adebola, Sadikot, Ruxana, Hoth, J Jason, Yoza, Barbara, Festic, Emir, Kaufman, David, Bajwa, Ednan, Malhotra, Atul, Thompson, B Taylor, Christiani, David C, Cengiz, Melike, Yilmaz, Murat, Anderson, Harry, Tchorz, Kathryn, McCarthy, Mary C, Uddin, David, Iscimen, Remzi, Dabbagh, Ousama, Kallenbach, Nena, Esper, Anette, Martin, Greg, Bajwa, Ednan K. , Douglas, Ivor S. , Frendl, György , Chang, Steven Y. , Anderson, Harry L, (USCIITG-LIPS), on behalf of the United States Critical Illness and Injury Trials Group: Lung Injury Prevention Study Investigators, (USCIITG-LIPS), the United States Critical Illness and Injury Trials Group: Lung Injury Prevention Study Investigators, Talmor, Daniel S, Bender, S Patrick, Garcia, Mauricio, Hou, Peter C, Barry, Jonathan M, Shempp, Iam, Malhotra, Atul, Frendl, Gyorgy, Ahmed, Adil, Gajic, Ognjen, Malinchoc, Michael, Kor, Daryl J, Afessa, Bekele, Cartin-Ceba, Rodrigo, Gong, Michelle Ng, Gentile, Nina T, Stevenson, Karen, Freeman, Brent, Srinivasan, Sujatha, Sevransky, Jonathan, Chang, Steven Y, Patrawalla, Amee, Elie, Carmelle, Hamdani, Irram, Seiden, Jason, Douglas, Ivor, Mikkelsen, Mark, Christie, Jason D, Gaieski, David F, Lanken, Paul, Meyer, Nuala, Sha, Chirag, Park, Pauline K, Harris, Julie, Napolitano, Lena, Raghavendran, Krishnan, Hyzy, Robert C, Blum, James, Watkins, Timothy R, Deem, Steven, Treggiari, Miriam, Adesanya, Adebola, Sadikot, Ruxana, Hoth, J Jason, Yoza, Barbara, Festic, Emir, Kaufman, David, Bajwa, Ednan, Malhotra, Atul, Thompson, B Taylor, Christiani, David C, Cengiz, Melike, Yilmaz, Murat, Anderson, Harry, Tchorz, Kathryn, McCarthy, Mary C, Uddin, David, Iscimen, Remzi, Dabbagh, Ousama, Kallenbach, Nena, Esper, Anette, Martin, Greg

Mayo Clinic

Respiratory Care | April 6, 2013 | Volume: 58 | Issue: 4 | Pages: 578-588

10.4187/respcare.01755 | PMID 22906363 Get It

Outcomes of Severe Sepsis and Septic Shock Patients on Chronic Antiplatelet Treatment: A Historical Cohort Study
Valerio-Rojas, Juan Carlos , Jaffer, Insara J., Kor, Daryl J. , Cartin‐Ceba, Rodrigo , Gajic, Ognjen

Mayo Clinic

Critical Care Research and Practice | February 20, 2013 | Volume: 2013 | Issue: No issue available | Pages: 1-9

10.1155/2013/782573 | PMID 23509620 Get It

Background. Sepsis is characterized by dysfunctional activation of platelets, and antiplatelet therapy could improve the outcomes of septic patients.Methods. We performed a retrospective cohort study of severe sepsis or septic shock adult patients. Outcomes of patients on antiplatelet therapy were compared to those that were not taking antiplatelet therapy by univariate analysis followed by a propensity score analysis based on the probability of receiving antiplatelet therapy.Results. Of 651 patients included in the study 272 (42.8%) were on antiplatelet therapy before the development of severe sepsis or septic shock. After adjusting for important confounding variables antiplatelet therapy was not associated with a decreased risk of hospital mortality (odds ratio 0.73, 95% confidence interval 0.46–1.16). Antiplatelet therapy was associated with a decreased incidence of acute respiratory distress syndrome/acute lung injury (odds ratio 0.50, 95% confidence interval 0.35–0.71) and reduced need of mechanical ventilation (odds ratio 0.62, 95% confidence interval 0.45–87). Incidence of acute kidney injury was similar between both groups (odds ratio 1.08, 95% confidence interval 0.73–1.59).Conclusions. The use of antiplatelet therapy before the diagnosis of severe sepsis or septic shock was not associated with decreased hospital mortality. Antiplatelet therapy was associated with a decreased incidence of acute lung injury/acute respiratory distress syndrome.
Risk Factors for Development of Acute Kidney Injury in Critically Ill Patients: A Systematic Review and Meta-Analysis of Observational Studies
Cartin‐Ceba, Rodrigo , Kashiouris, Markos , Plataki, Maria , Kor, Daryl J. , Casey, Edward T., Gajic, Ognjen

Mayo Clinic

Critical Care Research and Practice | November 26, 2012 | Volume: 2012 | Issue: No issue available | Pages: 1-15

10.1155/2012/691013 | PMID 23227318 Get It

Background. Acute kidney injury (AKI) is a frequent complication of critically ill patients. The impact of different risk factors associated with this entity in the ICU setting is unknown.Objectives. The purpose of this research was to assess the risk factors associated with the development of AKI in critically ill patients by meta-analyses of observational studies.Data Extraction. Two reviewers independently and in duplicate used a standardized form to collect data from published reports. Authors were contacted for missing data. The Newcastle-Ottawa scale assessed study quality.Data Synthesis. Data from 31 diverse studies that enrolled 504,535 critically ill individuals from a wide variety of ICUs were included. Separate random-effects meta-analyses demonstrated a significantly increased risk of AKI with older age, diabetes, hypertension, higher baseline creatinine, heart failure, sepsis/systemic inflammatory response syndrome, use of nephrotoxic drugs, higher severity of disease scores, use of vasopressors/inotropes, high risk surgery, emergency surgery, use of intra-aortic balloon pump, and longer time in cardiopulmonary bypass pump.Conclusion. The best available evidence suggests an association of AKI with 13 different risk factors in subjects admitted to the ICU. Predictive models for identification of high risk individuals for developing AKI in all types of ICU are required.
Long-Term Survival in Patients With Tracheostomy and Prolonged Mechanical Ventilation in Olmsted County, Minnesota
Kojicic, Marija, Li, Guangxi , Ahmed, Adil , Thakur, Lokendra , Trillo‐Alvarez, Cesar , Cartin‐Ceba, Rodrigo , Gay, Peter C. , Gajić, Ognjen, Vukoja, Marija , Kojicic, Marija, Li, Guangxi

Mayo Clinic

Respiratory Care | October 31, 2011 | Volume: 56 | Issue: 11 | Pages: 1765-1770

10.4187/respcare.01096 | PMID 21605480 Get It

BACKGROUND: An increasing number of patients require prolonged mechanical ventilation (PMV), which is associated with high morbidity and poor long-term survival, but there are few data regarding the incidence and outcome of PMV patients from a community perspective. METHODS: We retrospectively reviewed the electronic medical records of adult Olmsted county, Minnesota, residents admitted to the intensive care units at the 2 Mayo Clinic Rochester hospitals from January 1, 2003, to December 31, 2007, who underwent tracheostomy for PMV. RESULTS: Sixty-five patients, median age 68 years (interquartile range [IQR] 49–80 y), 39 male, underwent tracheostomy for PMV, resulting in an age-adjusted incidence of 13 (95% CI 10–17) per 100,000 patient-years at risk. The median number of days on mechanical ventilation was 24 days (IQR 18–37 d). Forty-six patients (71%) survived to hospital discharge, and 36 (55%) were alive at 1-year follow-up. After adjusting for age and baseline severity of illness, the presence of COPD was independently associated with 1-year mortality (hazard ratio 3.4, 95% CI 1.4–8.2%). CONCLUSIONS: There was a considerable incidence of tracheostomy for PMV. The presence of COPD was an independent predictor of 1-year mortality.
Timing of the Onset of Acute Respiratory Distress Syndrome: A Population-Based Study
Shari, G, Kojicic, Marija, Li, Guangxi , Cartin‐Ceba, Rodrigo , Trillo‐Alvarez, Cesar , Kashyap, Rahul , Dong, Yue , Poulose, Jaise T, Herasevich, Vitaly , Garza, Javier A Cabello, Vukoja, Marija , Kojicic, Marija, Poulose, JT, Garza, JA Cabello, Gajic, Ognjen , Kashyap, Rahul , Li, Guangxi , Herasevich, Vitaly , Dong, Yue

Mayo Clinic

Respiratory Care | May 2, 2011 | Volume: 56 | Issue: 5 | Pages: 576-582

10.4187/respcare.00901 | PMID 21276315 Get It

BACKGROUND: Many patients with acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) have had recent healthcare interventions prior to developing ALI/ARDS. OBJECTIVE: To determine the timing of ALI/ARDS onset in relation to hospital admission and other healthcare interventions. METHODS: We conducted a population-based observational cohort study with a validated electronic surveillance tool, and identified patients with possible ALI/ARDS among critically ill adults at Mayo Clinic hospitals that provide critical care services for Olmsted County, Minnesota, in 2006. Trained investigators independently reviewed electronic medical records and confirmed the presence and timing of ALI/ARDS based on the American-European consensus definition. RESULTS: Of 124 episodes of ALI in 118 patients, only 5 did not fulfill the ARDS criteria. The syndrome developed a median 30 hours (IQR 10–82 h) after hospital admission in 79 patients (67%). ARDS was present on admission in 39 patients (33%), of whom 14 had recent hospitalization, 6 were transferred from nursing homes, and 3 had recent out-patient contact (1 antibiotic prescription, 1 surgical intervention, and 1 chemotherapy). Only 16 ARDS patients (14%) did not have known recent contact with a healthcare system. Compared to ARDS on admission, hospital-acquired ARDS was more likely to occur in surgery patients (54% vs 15%, P < .001), and had longer adjusted hospital stay (mean difference 8.9 d, 95% CI 0.3–17.4, P = .04). CONCLUSIONS: ARDS in the community most often develops either during hospitalization or in patients who recently had contact with a healthcare system. These findings have important implications for potential preventive strategies.
Eight-Year Trend of Acute Respiratory Distress Syndrome: A Population-based Study in Olmsted County, Minnesota
Li, Guangxi , Malinchoc, Michael, Cartin‐Ceba, Rodrigo , Venkata, Chakradhar , Kor, Daryl J. , Peters, Steve G. , Hubmayr, Rolf D., Gajic, Ognjen , Li, Guangxi

Mayo Clinic

American Journal of Respiratory and Critical Care Medicine | August 6, 2010 | Volume: 183 | Issue: 1 | Pages: 59-66

10.1164/rccm.201003-0436oc | PMID 20693377 Get It

Abstract Rationale Significant progress has been made in understanding the pathogenesis of acute respiratory distress syndrome (ARDS). Recent advances in hospital practice may have reduced the incidence of this lethal syndrome. Objectives To observe incidence trends and associated outcomes of ARDS. Methods This population-based cohort study was conducted in Olmsted County, Minnesota. Using a validated screening protocol, investigators identified intensive care patients with acute hypoxemia and bilateral pulmonary infiltrates. The presence of ARDS was independently confirmed according to American-European Consensus Conference criteria. The incidence of ARDS and associated outcomes were compared over the 8-year study period (2001–2008). Measurements and Main Results Over the 8-year period, critically ill Olmsted County residents presented with increasing severity of acute illness, a greater number of comorbidities, and a higher prevalence of major predisposing conditions for ARDS. The ARDS incidence decreased significantly from 82.4 to 38.9 per 100,000 person-years during the study period (P &lt; 0.001). A decline in hospital-acquired ARDS (P &lt; 0.001) was responsible for the fall in the incidence density with no change on admission (P = 0.877). Overall, mortality and hospital and intensive care unit lengths of stay decreased over time (P &lt; 0.001), whereas the ARDS case-fatality did not change significantly. Conclusions Despite an increase in patients' severity of illness, number of comorbidities, and prevalence of major ARDS risk factors, the incidence of ARDS in this suburban community decreased by more than half. Correlation of the observed findings with changes in health care delivery may have important implications for the planning of acute care services in other regions.
24-Hour On-Site Intensivist in the Intensive Care Unit: Yes
Cartin‐Ceba, Rodrigo , Bajwa, Ednan K.

Mayo Clinic

American Journal of Respiratory and Critical Care Medicine | June 17, 2010 | Volume: 181 | Issue: 12 | Pages: 1279-1280

10.1164/rccm.201004-0676ed | PMID 20558637 Get It

Dyspnea and Wheezing after Adenosine Injection in a Patient with Eosinophilic Bronchitis
Cartin‐Ceba, Rodrigo , Aubry, Marie Christine, Lim, Kaiser G.

Mayo Clinic

Case Reports in Medicine | November 8, 2009 | Volume: 2009 | Issue: No issue available | Pages: 1-4

10.1155/2009/356462 | PMID 19902011 Get It

A 58-year-old nonsmoker female was referred for evaluation of chronic cough of 13 months duration. After an initial work-up, the patient was diagnosed to have chronic cough due to eosinophilic bronchitis. The diagnostic work-up for eosinophilic bronchitis and bronchial biopsy is discussed. Eosinophilic bronchitis is differentiated from asthma. In addition, the patient developed dyspnea, flushing, and wheezing after the administration of adenosine during a cardiac stress test in spite of a negative methacholine challenge. This indirect stimulus of airway hyperresponsiveness suggests the possible involvement of mast cells in eosinophilic bronchitis.