By: Weston Hampton, MD PGY3
Reviewed by: Tiffany Sigal, MD Sepsis is one of the most common causes of death worldwide, and for our patients in the United States it accounts for one of the highest rates of in-hospital mortality costing the healthcare system an estimated $24 billion annually. In attempts to curb this burden and improve patient safety, the Surviving Sepsis Campaign was launched in 2001 to more appropriately define sepsis and to determine appropriate treatment guidelines. In March of 2004, the first set of guidelines was published with goals of antibiotics within 6 hours, hemoglobin and blood glucose goals, and extensive fluid resuscitation (around 40- 60mL/kg crystalloid). These guidelines continued to be revised until they were widely endorsed in 2008, with the addition of lactic acid levels as a major biomarker to guide therapy. Surviving sepsis early management bundles were put forward as a requirement by the Center for Medicare/Medicaid Services (CMS) in 2015 as an “all or nothing” measure, meaning that if specific metrics were not met in the treatment of septic patients, the hospital would not receive reimbursement for the patient’s care. This highlights one of the major problems with sepsis care in the United States: it is an all or nothing metric that is heavily enforced by hospitals in attempts to be properly compensated, however the evidence in these guidelines is often out of date. Recent attempts at guidance in sepsis treatment has been dynamic and challenging, beginning with the concept of early goal-directed therapy (EGDT) in 2001. This concept attempted to use central venous pressure, mean arterial pressure, and venous oxygen saturation as resuscitative markers. While these metrics ultimately were proven less useful in the sepsis treatment, EGDT was adopted by the Surviving Sepsis Campaign with patients at this point in time receiving four to five liters of crystalloid within the first 24 hours. Large trials in the US, Australia, and England (known as the ProCESS, ARISE, and ProMISe trials respectively) debunked the use of EGDT, showing no mortality benefit and increased length of ICU. In fact, use of early goal- directed therapy demonstrated substantial amounts of fluid overload in treated patients in subsequent studies. That brings us to the most recent Surviving Sepsis Guidelines published in November 2021. Resuscitation with 30mL/kg IV crystalloid has moved from strong to weak recommendation when compared to prior, however continues to be a metric enforced for CMS compensation at the time of this writing. CMS has officially stated “there are no exclusions to the 30mL/kg amount based on co-morbidities such as heart failure, end-stage renal disease, or any other condition.” Other pertinent updates in the recent changes include starting vasopressors peripherally, favoring balanced crystalloids over normal saline, and administrating IV corticosteroids in patients with persistent vasopressor requirement. Additionally, as of January 2022, clinicians may give less than 30 cc/kg of crystalloid if they thoroughly document the indication for less fluid in a given patient. While many of these updates are reassuring and guidelines should be followed, it is still best to be mindful in the treatment of these critical patients. References:
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June 2022
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