# The Global Impact of Sepsis: Epidemiology, Recognition, Management, and Health System Challenges

**Authors:** Luigi La Via, Salvatore Ferlito, Maria Stella Di Modica, Andrea Marino, Giuseppe Nunnari, Bruno Cacopardo, Jerome Rene Lechien, Mario Lentini, Salvatore Lavalle, Giancarlo Carmelo Botto, Paolo Buscema, Loris Gruppuso, Antonino Maniaci

PMC · DOI: 10.3390/epidemiologia7010020 · Epidemiologia · 2026-02-03

## TL;DR

Sepsis is a leading cause of death globally, and addressing challenges in diagnosis, treatment, and health systems is critical to reducing its impact.

## Contribution

This paper provides a comprehensive review of sepsis epidemiology, diagnostics, treatment, and health system challenges, emphasizing the need for global equity in care.

## Key findings

- qSOFA and SOFA tools have limited sensitivity in diverse clinical settings.
- Rapid diagnostics like mNGS and AI-based devices improve detection but face cost and infrastructure barriers.
- Delays in antibiotic treatment increase mortality risk by 6–10% per hour.

## Abstract

Background: Sepsis constitutes a major healthcare burden worldwide, with an estimated 48.9 million incident cases and 11.0 million deaths in 2017, accounting for nearly one-fifth of all global deaths. Even with advances in definitions and guidelines, significant inequalities persist in awareness, early treatment, and health system readiness. Methods: We performed a structured narrative review of epidemiology studies, clinical case definitions, diagnostic approaches, stewardship interventions, and health system reports. Both electronic sources (PubMed, Web of Science, Embase, Scopus) and grey literature (World Health Organization [WHO], National Institute for Health and Care Excellence [NICE], Society Critical Care [SSC]) were explored. Evidence incorporated themes were organized across recognition, diagnostics, antimicrobial therapy, organ support, guidelines, and health system determinants. Results: Measurement tools, including quick Sequential Organ Failure Assessment (qSOFA) and Sequential Organ Failure Assessment (SOFA), exhibited suboptimal sensitivity and utility in varied clinical environments. Biomarkers (procalcitonin, presepsin, CD64) and rapid molecular diagnostics, including metagenomic next-generation sequencing (mNGS) and AI-based devices, enhance detection but are limited by cost and infrastructure constraints. Each hour of delay in antibiotic therapy is associated with a 6–10% increased risk of mortality, underscoring the importance of stewardship, including the incorporation of empiric regimens with rapid de-escalation. Health system bottlenecks—human resources, funding, infrastructure—continue to be a significant determinant of outcomes, especially in low- and middle-income countries. Conclusions: Attaining the 2030 WHO targets for sepsis involves precision diagnostics, adaptable guidelines, stewardship frameworks, and resilient health systems. Fair application and resource allocation are crucial to lower the incidence and mortality worldwide.

## Full-text entities

- **Genes:** CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, FCGR1A (Fc gamma receptor Ia) [NCBI Gene 2209] {aka CD64, CD64A, FCG1, FCGR1, FCRI, FcgammaRI}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** neuropathy (MESH:D009422), Cognitive sequelae (MESH:D003072), Adult Sepsis (MESH:D018805), Illnesses (MESH:D002908), Long (MESH:D000094024), deficits in memory and executive function (MESH:D008569), infectious disease (MESH:D003141), arterial hypotension (MESH:D007022), HIV (MESH:D015658), septic shock (MESH:D012772), chronic fatigue (MESH:D015673), fungal (MESH:D009181), neuromuscular polyneuropathy (MESH:D009468), septic (MESH:D001170), ARDS (MESH:D012128), Maternal (MESH:D000079262), PTSD (MESH:D013313), fatigue (MESH:D005221), systemic (MESH:D015619), diarrhea (MESH:D003967), postpartum (MESH:D006473), dysfunction (MESH:D006331), AMR (MESH:C565965), parasitic and non-infectious (MESH:D000073296), pneumonia (MESH:D011014), TB (MESH:D014376), Maternal/Neonatal Sepsis (MESH:D000071074), bacterial infection (MESH:D001424), ED (MESH:D004630), Organ Failure (MESH:D009102), hypoxic (MESH:D002534), depression (MESH:D003866), renal impairment (MESH:D007674), edema (MESH:D004487), GBD (MESH:D001037), anxiety (MESH:D001007), pulmonary injury (MESH:D055370), infection (MESH:D007239), Post-Sepsis Syndrome (MESH:D018746), coagulopathy (MESH:D001778), cardiovascular disease (MESH:D002318), diabetes (MESH:D003920), muscle weakness (MESH:D018908), lactic acidosis (MESH:D000140), brain dysfunction (MESH:D001927), influenza (MESH:D007251), death (MESH:D003643), DBN (MESH:D000092242), malnutrition (MESH:D044342), Surviving Sepsis (MESH:D011475), shock (MESH:D012769), Disease (MESH:D004194), injury to (MESH:D014947), term disability (MESH:D000088562), inflammation (MESH:D007249), metastases (MESH:D009362), critical illness (MESH:D016638)
- **Chemicals:** glucose (MESH:D005947), norepinephrine (MESH:D009638), dopamine (MESH:D004298), Vit C. (MESH:D001205), heparin (MESH:D006493), carbapenem (MESH:D015780), H2O (MESH:D014867), steroids (MESH:D013256), lactate (MESH:D019344), catecholamine (MESH:D002395), cephalosporins (MESH:D002511), hydrocortisone (MESH:D006854), thiamine (MESH:D013831), aminoglycosides (MESH:D000617), oxygen (MESH:D010100), SSC (-)
- **Species:** Enterobacteriaceae (enterobacteria, family) [taxon 543], Klebsiella pneumoniae (species) [taxon 573], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

74 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921907/full.md

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Source: https://tomesphere.com/paper/PMC12921907