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1.
Cureus ; 15(6): e40323, 2023 Jun.
Article in English | MEDLINE | ID: mdl-37448408

ABSTRACT

Superior vena cava (SVC) syndrome is a constellation of clinical signs and symptoms secondary to obstruction of the SVC. The most common etiology is malignancy. However, the incidence of device-related SVC syndrome is increasing. The current management for device-related SVC syndrome includes open surgical intervention, endovascular repair, or systemic anticoagulation. We present a case of a 95-year-old female who developed SVC syndrome due to thrombosis secondary to pacemaker leads. She was treated conservatively due to her frailty and comorbid conditions. We discuss the evolving etiology of SVC syndrome, the most common presenting signs and symptoms, and a variety of potential treatments for non-malignant SVC syndrome. We also provide an example of when conservative management for chronic device-related SVC syndrome is appropriate.

2.
N Engl J Med ; 351(9): 884-92, 2004 Aug 26.
Article in English | MEDLINE | ID: mdl-15329426

ABSTRACT

BACKGROUND: Preclinical studies suggest that exogenous surfactant may be of value in the treatment of the acute respiratory distress syndrome (ARDS), and two phase 2 clinical trials have shown a trend toward benefit. We conducted two phase 3 studies of a protein-containing surfactant in adults with ARDS. METHODS: In two multicenter, randomized, double-blind trials involving 448 patients with ARDS from various causes, we compared standard therapy alone with standard therapy plus up to four intratracheal doses of a recombinant surfactant protein C-based surfactant given within a period of 24 hours. RESULTS: The overall survival rate was 66 percent 28 days after treatment, and the median number of ventilator-free days was 0 (68 percent range, 0 to 26); there was no significant difference between the groups in terms of mortality or the need for mechanical ventilation. Patients receiving surfactant had a significantly greater improvement in blood oxygenation during the initial 24 hours of treatment than patients receiving standard therapy, according to both univariate and multivariate analyses. CONCLUSIONS: The use of exogenous surfactant in a heterogeneous population of patients with ARDS did not improve survival. Patients who received surfactant had a greater improvement in gas exchange during the 24-hour treatment period than patients who received standard therapy alone, suggesting the potential benefit of a longer treatment course.


Subject(s)
Pulmonary Surfactant-Associated Protein C/therapeutic use , Pulmonary Surfactants/therapeutic use , Respiratory Distress Syndrome/drug therapy , APACHE , Analysis of Variance , Causality , Double-Blind Method , Female , Humans , Logistic Models , Male , Middle Aged , Oxygen/blood , Pulmonary Surfactant-Associated Protein C/adverse effects , Pulmonary Surfactants/adverse effects , Recombinant Proteins/adverse effects , Recombinant Proteins/therapeutic use , Respiration, Artificial , Respiratory Distress Syndrome/etiology , Respiratory Distress Syndrome/mortality , Respiratory Distress Syndrome/therapy , Survival Rate , Treatment Failure
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