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Peters, Steve G.

0000-0001-8438-3261

Mayo Clinic

Mayo Clinic

Citations 23

Outcome of Diffuse Alveolar Hemorrhage in Hematopoietic Stem Cell Transplant Recipients
Afessa, Bekele, Tefferi, Ayalew , Litzow, Mark R. , Peters, Steve G.

American Journal of Respiratory and Critical Care Medicine | November 15, 2002 | Volume: 166 | Issue: 10 | Pages: 1364-1368

10.1164/rccm.200208-792oc Get It

Abstract Previous studies have reported mortality rates of about 80% in hematopoietic stem cell transplant recipients with diffuse alveolar hemorrhage. This retrospective study describes the clinical course of 48 such patients: mean age 47.7 years, 52% autologous transplant and 67% peripheral stem cell source. The hemorrhage occurred within one month of transplant in 28 patients. Symptoms included dyspnea in 92%, fever in 67%, cough in 56%, and hemoptysis in 15%. Intensive care unit admission was required in 85% and mechanical ventilation in 77%. Most of the patients were treated with intravenous methylprednisolone 1 g daily for 3 days and then tapered off after a median of 22 days. The hospital mortality was 48%. The cause of death was respiratory failure in 15 of the 23 deaths. Mortality was 28% in autologous compared with 70% in allogeneic transplant recipients (p = 0.0040). The mortality rate of patients whose hemorrhage occurred within the first 30 days of transplant was 32% compared with 70% of those with late hemorrhage (p = 0.0096). This study shows that survival rate of hematopoietic stem cell transplant recipients with diffuse alveolar hemorrhage is better than previously reported, and that early onset and autologous transplant are favorable prognostic indicators.
Outcome of Patients with Idiopathic Pulmonary Fibrosis Admitted to the Intensive Care Unit
Saydain, Ghulam , Islam, Ashiq, Afessa, Bekele, Ryu, Jay H. , Peters, Steve G. , Scott, James G. , Ryu, Jay H

American Journal of Respiratory and Critical Care Medicine | September 13, 2002 | Volume: 166 | Issue: 6 | Pages: 839-842

10.1164/rccm.2104038 Get It

Abstract This retrospective study describes the clinical course of 38 patients with idiopathic pulmonary fibrosis (IPF) admitted to the intensive care unit (ICU). There were 25 males and 13 females who were the mean age of 68.3 ± 11.5 years. Twenty patients were on corticosteroids at the time of admission to the hospital, and 24 had been on home oxygen therapy. The most common reason for ICU admission was respiratory failure. The Acute Physiology and Chronic Health Evaluation III–predicted ICU and hospital mortality rates were 12% and 26%, whereas the actual ICU and hospital mortality rates were 45% and 61%, respectively. We did not find significant differences in pulmonary function or echocardiogram findings between survivors and nonsurvivors. Mechanical ventilation was used in 19 patients (50%). Sepsis developed in nine patients. Multiple organ failure developed in 14% of the survivors and in 43% of the nonsurvivors (p = 0.14). Ninety-two percent of the hospital survivors died at a median of 2 months after discharge. These findings suggest that patients with IPF admitted to the ICU have poor short- and long-term prognosis. Patients with IPF and their families should be informed about the overall outlook when they make decisions about life support and ICU care.
Diffuse Alveolar Hemorrhage in Hematopoietic Stem Cell Transplant Recipients
Afessa, Bekele, Tefferi, Ayalew , Litzow, Mark R. , Krowka, Michael J. , Wylam, Mark E. , Peters, Steve G.

American Journal of Respiratory and Critical Care Medicine | August 30, 2002 | Volume: 166 | Issue: 5 | Pages: 641-645

10.1164/rccm.200112-141cc Get It