Experimental and emerging therapies for sepsis and septic shock

被引:16
作者
Añel, RL
Kumar, A
机构
[1] Rush Presbyterian St Lukes Med Ctr, Sect Crit Care Med, Chicago, IL 60612 USA
[2] Cook County Hosp, Rush Med Coll, Chicago, IL USA
关键词
APC; ATIII; apoptosis; caspase; complement; hydrocortisone; ibuprofen; NO; NOS; PAF; sepsis; septic shock;
D O I
10.1517/13543784.10.8.1471
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The underlying principles of sepsis therapy have remained unchanged for decades. These include: prompt institution of antimicrobial agents aimed at the inciting pathogen, source control directed at removal of the infection nidus whenever possible, and support of organ dysfunction. Despite advances in antibiotics, surgical techniques and organ support technology, the morbidity and mortality from sepsis-related diseases have remained substantially unchanged (30 - 50%). Immunomodulation of the inflammatory cascade has been suggested as a crucial but inadequately addressed element in the treatment of sepsis. The list of potential therapeutic targets has been growing as more and more mediators are identified in the pathogenesis of sepsis. To date, numerous anti-inflammatory agents, found to have favourable effects in animal models of septic shock, have been tested in a number of clinical trials on thousands of patients. in this first of a three part series, we go through some of the background and current strategies in sepsis therapy. In this review, we include the two novel therapies that have shown clear survival benefit in large, randomised, placebo-controlled, multicentre trials, low-dose steroids and recombinant activated protein C. Also included in this review are studies on antithrombin III, platelet-activating factor antagonists, complement modulators, nitric oxide synthase inhibitors and caspase inhibitors (apoptosis inhibitors).
引用
收藏
页码:1471 / 1485
页数:15
相关论文
共 123 条
  • [1] Tissue factor inhibition and clinical trial results of tissue factor pathway inhibitor in sepsis - Question and answer session after scientific review
    Vincent, JL
    Abraham, E
    Esmon, C
    Hack, CE
    [J]. CRITICAL CARE MEDICINE, 2000, 28 (09) : S33 - S33
  • [2] ANEL R, 2001, CONNS CURRENT THERAP, P56
  • [3] A 3-level prognostic classification in septic shock based on cortisol levels and cortisol response to corticotropin
    Annane, D
    Sébille, V
    Troché, G
    Raphaël, JC
    Gajdos, P
    Bellissant, E
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (08): : 1038 - 1045
  • [4] Annane D, 2000, CRIT CARE MED, V28, pA46
  • [5] Therapeutic inhibition of the complement system. Y2K update
    Asghar, SS
    Pasch, MC
    [J]. FRONTIERS IN BIOSCIENCE-LANDMARK, 2000, 5 : E63 - E82A
  • [6] IL-10 mediation of activation-induced Th1 cell apoptosis and lymphoid dysfunction in polymicrobial sepsis
    Ayala, A
    Chung, CS
    Song, GY
    Chaudry, IH
    [J]. CYTOKINE, 2001, 14 (01) : 37 - 48
  • [7] BAKKER J, 1998, CRIT CARE MED S1, V26, pA63
  • [8] Balk R. A., 1995, INTENS CARE MED, V21, P17
  • [9] Antithrombin III (ATIII) replacement therapy in patients with sepsis and/or postsurgical complications: a controlled double-blind, randomized, multicenter study
    Baudo, F
    Caimi, TM
    de Cataldo, F
    Ravizza, A
    Arlati, S
    Casella, G
    Carugo, D
    Palareti, G
    Legnani, C
    Ridolfi, L
    Rossi, R
    D'Angelo, A
    Crippa, L
    Giudici, D
    Gallioli, G
    Wolfler, A
    Calori, G
    [J]. INTENSIVE CARE MEDICINE, 1998, 24 (04) : 336 - 342
  • [10] Efficacy and safety of recombinant human activated protein C for severe sepsis.
    Bernard, GR
    Vincent, JL
    Laterre, P
    LaRosa, SP
    Dhainaut, JF
    Lopez-Rodriguez, A
    Steingrub, JS
    Garber, GE
    Helterbrand, JD
    Ely, EW
    Fisher, CJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) : 699 - 709