Surviving Sepsis Is Not Enough, Time to Confront Post-sepsis Syndrome, A Narrative Review
DOI:
https://doi.org/10.60186/RJCCN.16Keywords:
Sepsis, Post-Sepsis Syndrome, Critical Care, Quality of Life, RehabilitationAbstract
While global advances in sepsis care have reduced acute mortality,
many survivors face a persistent burden of Post-Sepsis Syndrome
(PSS), a complex condition encompassing physical, cognitive,
psychological, immunologic, and social sequelae. Despite its
prevalence, post-sepsis care remains fragmented and under
recognized within routine critical care pathways.
Relevant literature on post-sepsis outcomes was reviewed
through major scientific databases, focusing on studies exploring
the physical, cognitive, psychological, immunologic, and social
consequences of sepsis. Observational, interventional, and review
articles contributing to the understanding of post-sepsis syndrome
were evaluated, and findings were synthesized narratively across
key thematic domains. Recent multi-center and population-based
studies reveal that over half of sepsis survivors experience at
least one PSS component within the first year after discharge.
Persistent fatigue, neuromuscular weakness, cognitive dysfunction,
depression, anxiety, and increased susceptibility to infections
are the most common manifestations. Hospital readmission and
long-term functional decline remain frequent, while structured
follow-up and rehabilitation services are scarce. Awareness among
clinicians and policy frameworks addressing survivorship are
limited. The reduction of in-hospital sepsis mortality has unveiled
a new challenge; survivorship. Long-term recovery requires
coordinated and multidisciplinary care extending beyond ICU
discharge. Integrating PSS surveillance, rehabilitation programs,
and patient education into national sepsis strategies is essential
to improve functional outcomes and quality of life.