2013
DOI: 10.1111/trf.12328
|View full text |Cite
|
Sign up to set email alerts
|

Erythropoiesis‐stimulating agents: friends or foes?

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
4
0

Year Published

2014
2014
2020
2020

Publication Types

Select...
4
4

Relationship

1
7

Authors

Journals

citations
Cited by 10 publications
(4 citation statements)
references
References 40 publications
(79 reference statements)
0
4
0
Order By: Relevance
“… 8 The use of pediatric blood tubes should be considered when appropriate, and the judicious use of intravenous iron and erythropoietin should also be considered in the postoperative period. 8 , 11 , 13 , 14 If acute postoperative bleeding is suspected, the surgeon should consider reoperation promptly to identify and treat the source of bleeding. 8 Although we do not routinely follow hemoglobin levels in the postoperative period in a stable patient, studies have shown a low risk of postoperative mortality in upper nadir hemoglobin ranges of 7–8 g/dL and much higher risk in lower ranges.…”
Section: Discussionmentioning
confidence: 99%
“… 8 The use of pediatric blood tubes should be considered when appropriate, and the judicious use of intravenous iron and erythropoietin should also be considered in the postoperative period. 8 , 11 , 13 , 14 If acute postoperative bleeding is suspected, the surgeon should consider reoperation promptly to identify and treat the source of bleeding. 8 Although we do not routinely follow hemoglobin levels in the postoperative period in a stable patient, studies have shown a low risk of postoperative mortality in upper nadir hemoglobin ranges of 7–8 g/dL and much higher risk in lower ranges.…”
Section: Discussionmentioning
confidence: 99%
“…Additionally, we recommend cautious use of ESAs in patients whose transfusion requirements have not decreased or who have failed to realize an increase in hemoglobin of greater than 1 g/dL after 6–8 weeks of dosing. Deleterious effects of ESAs, while originally thought to be due to increased blood viscosity (with or without subsequent platelet activation ) or agonistic effect on tumor cell epo receptors, may actually be due to unopposed circulating plasma erythropoietin . This hypothesis may help to explain reasons for increased VTE and mortality risk in patients with Hb values in the low or normal range, who received higher doses due to “targeting” a higher Hb value.…”
Section: Rbc Transfusion Versus Esasmentioning
confidence: 99%
“…Erythropoiesis‐stimulating agents (ESAs) such as recombinant human erythropoietin increase the hemoglobin preoperatively and may be a useful adjuvant in certain situations such as a high‐risk group for bleeding (for example weight <10 kg, syndromic patient with co‐morbidities, or preoperative anemia; Hgb <10 g·dl −1 ) . ESA clinical protocols of epoetin alfa 600IU kg·week −1 subcutaneously for 3–4 weeks in divided doses, with iron, vitamin B12, vitamin E, and folic acid oral supplementation have been described.…”
Section: Blood Conservation Techniquesmentioning
confidence: 99%