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Scientific and clinical challenges in sepsis.

Publication ,  Journal Article
Ulloa, L; Brunner, M; Ramos, L; Deitch, EA
Published in: Current pharmaceutical design
January 2009

Advances in intensive care and antibiotics have prevented the spread of some infections, though sepsis mortality rates remain high. With failure of over thirty clinical trials, sepsis remains a scientific and clinical challenge in modern medicine. Sepsis is defined by the clinical signs of a systemic inflammatory response to infection. "Severe sepsis" is when these symptoms are associated with multiple organ dysfunction. These definitions of sepsis may be too broad and common to heterogeneous groups of patients who do not necessarily have the same disorder. This consideration has become especially evident in the clinical trials that have failed to obtain consistent results in similar studies of patients diagnosed with severe sepsis. In these trials, patients with infections caused by different microorganisms, and affecting different organs, have been combined under the general diagnosis of severe sepsis. The situation is analogous to attempting a clinical trial based on the general definition of cancer, combining all patients with tumor independent of the type of malignancy. In this consideration, it would not be very surprising that activated protein C, the only treatment in sepsis approved by the Food and Drug Administration, is projected for use in only a small subset of patients with severe sepsis. This article reviews novel inflammatory molecular aspects and the experimental anti-inflammatory strategies for sepsis, as they may represent particular pathological processes in specific subsets of patients.

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Published In

Current pharmaceutical design

DOI

EISSN

1873-4286

ISSN

1381-6128

Publication Date

January 2009

Volume

15

Issue

16

Start / End Page

1918 / 1935

Related Subject Headings

  • Sepsis
  • Nicotinic Agonists
  • Medicinal & Biomolecular Chemistry
  • Macrophage Migration-Inhibitory Factors
  • Lysophosphatidylcholines
  • Humans
  • HMGB1 Protein
  • Glucocorticoids
  • Clinical Trials as Topic
  • Caspase Inhibitors
 

Citation

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Ulloa, L., Brunner, M., Ramos, L., & Deitch, E. A. (2009). Scientific and clinical challenges in sepsis. Current Pharmaceutical Design, 15(16), 1918–1935. https://doi.org/10.2174/138161209788453248
Ulloa, Luis, Michael Brunner, Laura Ramos, and Edwin A. Deitch. “Scientific and clinical challenges in sepsis.Current Pharmaceutical Design 15, no. 16 (January 2009): 1918–35. https://doi.org/10.2174/138161209788453248.
Ulloa L, Brunner M, Ramos L, Deitch EA. Scientific and clinical challenges in sepsis. Current pharmaceutical design. 2009 Jan;15(16):1918–35.
Ulloa, Luis, et al. “Scientific and clinical challenges in sepsis.Current Pharmaceutical Design, vol. 15, no. 16, Jan. 2009, pp. 1918–35. Epmc, doi:10.2174/138161209788453248.
Ulloa L, Brunner M, Ramos L, Deitch EA. Scientific and clinical challenges in sepsis. Current pharmaceutical design. 2009 Jan;15(16):1918–1935.

Published In

Current pharmaceutical design

DOI

EISSN

1873-4286

ISSN

1381-6128

Publication Date

January 2009

Volume

15

Issue

16

Start / End Page

1918 / 1935

Related Subject Headings

  • Sepsis
  • Nicotinic Agonists
  • Medicinal & Biomolecular Chemistry
  • Macrophage Migration-Inhibitory Factors
  • Lysophosphatidylcholines
  • Humans
  • HMGB1 Protein
  • Glucocorticoids
  • Clinical Trials as Topic
  • Caspase Inhibitors