Ultrasound Therapy; Complications Clinical Trial
Official title:
Lung Ultrasound as an Evolving Tool in Detection of Extravascular Lung Water in Septic Cancer Patients.
Verified date | September 2018 |
Source | National Cancer Institute, Egypt |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
Sepsis is a common serious problem in surgical critical care units.Septic shock can be a consequence of severe sepsis with high mortality rate, in which there is major disturbance on the cellular, metabolic and circulatory levels.Patients who suffer from malignancy or under chemotherapeutic treatment are at higher risk of sepsis.Postoperative cancer patients carry both the risk of underlying malignancy with superimposed risk of major surgical procedure.]. Monitoring effective fluid resuscitation and patient's hemodynamic status is achieved through different techniques mainly by measuring central venous pressure (CVP), pulmonary artery occlusion pressure (PAOP) and transpulmonary thermodilution along with chest radiography analysis .This study aims to investigate the correlation between lung ultrasound and IVC collapsibility index in assessment of fluid responsiveness in cancer patients with septic shock.
Status | Completed |
Enrollment | 30 |
Est. completion date | August 30, 2018 |
Est. primary completion date | August 30, 2018 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Patients aged between (18 - 65) years. - Diagnosed with severe sepsis or septic shock according to the third international consensus definition (sepsis-3). - All of them underwent major abdominal oncologic surgeries. Exclusion Criteria: - ASA III and IV patients. - Patients with BMI>35. - Patients who suffered from chronic lung disease. - History of cardiac or renal problems. - Patients with lung cancer or pulmonary metastases. - Patients with inserted chest tubes. - Presence of subcutaneous emphysema. |
Country | Name | City | State |
---|---|---|---|
Egypt | Department of Anesthesia and Pain medicine.National Cancer Institute | Cairo |
Lead Sponsor | Collaborator |
---|---|
National Cancer Institute, Egypt |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Detection of B-lines | The number of B lines was scanned and a quadrant was considered to be positive when 3 or more B-Lines were recorded. A patient was defined to have positive B-lines (when 3 or more B-Lines are recorded in 3 or more quadrants). | 12 hours follow up |
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