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Fig 1.

PRISMA flow diagram for the study inclusion and exclusion process.

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Table 1.

Characteristics of the included studies.

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Table 1 Expand

Table 2.

Bias risk assessment and methodology of the meta-analysis.

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Table 2 Expand

Fig 2.

Forest plot demonstrating the proportion of patients who received transfusion (%).

Subgroup analysis according to (A) the iron dose and (B) period of intravenous iron therapy (IVIT) administration. CI, confidence interval; I2, statistical heterogeneity.

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Table 3.

Results of meta-analysis for the proportion of patients who received transfusion and units of RBCs transfused.

Sub-group analysis according to the dose of intravenous (IV) iron (low dose: ≤ 300 mg and high dose: > 400 mg), the period of intravenous iron therapy (IVIT) (pre-operative, post-operative, and perioperative periods), and the study design (RCTs vs. CCSs).

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Fig 3.

Forest plot showing the units of RBCs transfused (U/patient).

Subgroup analysis according to (A) iron dose and (B) period of intravenous iron therapy (IVIT). SD, standard deviation; CI, confidence interval; I2, statistical heterogeneity.

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Fig 3 Expand

Fig 4.

Recovery profiles: (A) length of hospital stay (days), (B) post-operative infections (%), (C) mortality (%). SD, standard deviation; CI, confidence interval; I2, statistical heterogeneity.

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Fig 4 Expand