Abstract | OBJECTIVE: DESIGN: Descriptive. SETTING: PATIENTS AND METHODS:
Intensive-care patients with the sepsis syndrome and shock or organ failure with a presumptive diagnosis of Gram-negative infection were eligible for treatment with HA-1A. We analysed and compared the results with those of the double-blind, randomized HA-1A study by Ziegler et al. RESULTS: Between May 1991 and March 1992, 27 patients were treated with HA-1A. The mortality rate was 59% (16/27). Among the 11 patients with a Gram-negative bacteraemia mortality was 7/11, much higher than in the Ziegler study (30%). In comparison with the HA-1A study we selected sicker patients: the mean APACHE II score was higher, 93% of our patients were in shock and 85% had organ failure. More patients presented with an intra-abdominal sepsis and mortality in this group was very high (11/14). In patients with a Gram-negative bacteraemia the delay between the onset of the sepsis syndrome and the administration of HA-1A was longer (median 22 h versus 14.3 h in the Ziegler study, mean 30 versus 20 h). CONCLUSION: HA-1A does not appear to be beneficial in critically ill patients with a longstanding sepsis syndrome, especially not if an intra-abdominal sepsis is apparent. Therefore, we decided not to use H-1A until additional data become available. Additional objective inclusion criteria are needed to improve the identification of the patient group that may benefit from treatment with HA-1A.
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Authors | L G Costongs, P Speelman, J J van Lieshout, S J van Deventer, M J Lubbers, H G Schipper |
Journal | Nederlands tijdschrift voor geneeskunde
(Ned Tijdschr Geneeskd)
Vol. 137
Issue 7
Pg. 355-60
(Feb 13 1993)
ISSN: 0028-2162 [Print] Netherlands |
Vernacular Title | Immunotherapie met de anti-endotoxine-antistof HA-1A (Centoxin) bij patiënten met het sepsissyndroom; matige resultaten na geprotocolleerde selectie van patiënten. |
PMID | 8437634
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
- Endotoxins
- Immunoglobulin G
- nebacumab
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Topics |
- Adolescent
- Adult
- Aged
- Antibodies, Monoclonal
(therapeutic use)
- Antibodies, Monoclonal, Humanized
- Clinical Trials as Topic
- Endotoxins
(immunology)
- Female
- Gram-Negative Bacterial Infections
(complications, therapy)
- Humans
- Immunoglobulin G
(therapeutic use)
- Male
- Middle Aged
- Multiple Organ Failure
(therapy)
- Sepsis
(etiology, mortality, therapy)
- Severity of Illness Index
- Shock, Septic
(therapy)
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