| Literature DB >> 34931280 |
Mikael Kangaspunta1, Jorma Mäkijärvi2, Selja Koskensalo2, Arto Kokkola2, Perttu Arkkila3, Tom Scheinin2, Suvi Rasilainen2.
Abstract
PURPOSE: Anemia is common among patients with colorectal cancer and is associated with an increased risk of complications and poorer survival rate. The main objective of our study was to determine the effect of preoperative intravenous iron supplementation therapy on the need for red blood cell transfusions, other postoperative complications, and length of hospital stay in colon cancer patients undergoing colon resection.Entities:
Keywords: Anemia; Colon cancer; Colorectal surgery; Intravenous iron
Mesh:
Substances:
Year: 2021 PMID: 34931280 PMCID: PMC8803765 DOI: 10.1007/s00384-021-04080-9
Source DB: PubMed Journal: Int J Colorectal Dis ISSN: 0179-1958 Impact factor: 2.571
The characteristics of the patients
| iv iron | Control | |
|---|---|---|
| Number of patients | 180 | 138 |
| Gender | ||
| Male (%) | 84 (46.7) | 72 (52.2) |
| Female (%) | 96 (53.3) | 66 (47.8) |
| Age (median [IQR]), years | 73.8 (66.9–80.1) | 76.0 (70.1–81.9) |
| BMI (median [IQR]), kg/m2 | 25.4 (23.1–29.1) | 25.8 (23.4–30.3) |
| Location of the tumor | ||
| Sigmoid colon (%) | 28 (15.6) | 39 (28.3) |
| Descending colon (%) | 2 (1.1) | 5 (3.6) |
| Splenic flexure (%) | 17 (9.4) | 2 (1.4) |
| Transverse colon (%) | 12 (6.7) | 18 (13.0) |
| Hepatic flexure (%) | 23 (12.8) | 6 (4.3) |
| Ascending colon (%) | 47 (26.2) | 39 (28.3) |
| Caecum (%) | 51 (28.4) | 29 (21.0) |
| Grade of the tumor | ||
| 1 (%) | 13 (7.2) | 13 (9.4) |
| 2 (%) | 138 (76.7) | 103 (74.6) |
| 3 (%) | 20 (11.1) | 14 (10.1) |
| 4 (%) | 0 (0) | 1 (0.7) |
| Unknown (%) | 9 (5.0) | 7 (5.1) |
| Stage | ||
| 1 (%) | 21 (11.7) | 23 (16.7) |
| 2 (%) | 82 (45.6) | 58 (42.0) |
| 3 (%) | 60 (33.3) | 41 (29.7) |
| 4 (%) | 17 (9.4) | 16 (11.6) |
| Type of the procedure | ||
| Laparoscopic (%) | 130 (72.2) | 95 (68.8) |
| Laparotomy (%) | 50 (27.8) | 43 (31.2) |
| Indication | ||
| Curative (%) | 168 (93.3) | 124 (89.9) |
| Palliative (%) | 12 (6.7) | 14 (10.1) |
| ASA classification | ||
| 1 (%) | 4 (2.2) | 2 (1.4) |
| 2 (%) | 63 (35.0) | 32 (23.2) |
| 3 (%) | 83 (46.1) | 76 (55.1) |
| 4 (%) | 30 (16.7) | 28 (20.3) |
| 5 (%) | 0 (0) | 0 (0) |
| Median (IQR) | 3 (2–3) | 3 (2.75–3) |
| Charlson Comorbidity Index | ||
| Median (IQR) | 6 (5–7) | 6 (5–8) |
| Adjuvant chemotherapy | ||
| Yes (%) | 78 (43.4) | 50 (36.2) |
| No (%) | 102 (56.7) | 88 (63.8) |
Outcome variables
| iv iron | Control | ||
|---|---|---|---|
| Red blood cells | |||
| Preoperatively (%) | 50 (27.8) | 28 (20.3) | 0.12 |
| Intraoperatively (%) | 28 (15.6) | 29 (21) | 0.21 |
| Postoperatively (%) | 21 (11.7) | 23 (16.7) | 0.20 |
| Red blood cell units | |||
| Preoperatively (mean ± SD) | 0.82 ± 1.6 | 0.57 ± 1.5 | 0.09 |
| Intraoperatively (mean ± SD) | 0.25 ± 0.69 | 0.28 ± 0.60 | 0.24 |
| Postoperatively (mean ± SD) | 0.22 ± 0.63 | 0.36 ± 1.0 | 0.22 |
| Other postoperative complications | |||
| Any complication (%) | 61 (33.9) | 62 (44.9) | 0.045 |
| Clavien-Dindo 1–2 complications only (%) | 30 (16.7) | 36 (26.1) | 0.04 |
| Clavien-Dindo 3–5 complications (%) | 31 (17.2) | 26 (18.8) | 0.71 |
| Comprehensive Complication Index | |||
| Mean ± SD | 8.55 ± 14.4 | 12.2 ± 20.1 | |
| Length of stay | |||
| Median (IQR) days | 4 (3–6) | 5 (3–8) | 0.19 |
| Over 7 days (%) | 34 (18.9) | 36 (26.1) | 0.13 |
| Mortality | |||
| 30 days (%) | 1 (0.6) | 3 (2.2) | 0.2 |
| 90 days (%) | 6 (3.3) | 6 (4.3) | 0.64 |
The laboratory test results of the patients
| IV-IST | Non-IV-IST | ||||||
|---|---|---|---|---|---|---|---|
| Pre-iron infusion | Preoperative | At discharge | One month postoperatively | Preoperative | At discharge | One month postoperatively | |
| Hb (mean ± SD), g/l | 99.2 ± 15.5 | 110 ± 12.5 | 108 ± 11.7 | 126 ± 12.1 | 113 ± 10.5 | 108 ± 9.6 | 119 ± 11.9 |
| MCV (mean ± SD), fl | 80.0 ± 8.5 | 83.4 ± 6.9 | 84.7 ± 5.8 | 87.6 ± 5.0 | 87.1 ± 6.7 | 87.4 ± 5.9 | 89.1 ± 5.8 |
| Thrombocytes (mean ± SD) × 109/l | 350 ± 106 | 322 ± 98 | 317 ± 117 | 273 ± 91.0 | 301 ± 104 | 324 ± 154 | 289 ± 103 |
| Creatinine (mean ± SD), μmol/l | 76.3 ± 18.4 | 75.8 ± 18.8 | 64.5 ± 16.7 | 72.7 ± 16.9 | 79.6 ± 24.7 | 70.1 ± 24.3 | 78.0 ± 23.0 |
| CEA (median [IQR]), μg/l | 2.95 (1.70–8.98) | 2.70 (1.50–6.48) | |||||
Mild (Clavien-Dindo score 1 or 2) complications other than RBCT
| Fever | 9 (5.0) | 6 (4.3) |
| Pneumonia | 7 (3.9) | 4 (2.9) |
| Nausea/vomiting | 6 (3.3) | 3 (2.2) |
| Hypokalemia | 3 (1.7) | 6 (4.3) |
| Atrial fibrillation | 4 (2.2) | 3 (2.2) |
| Wound infection | 3 (1.7) | 4 (2.9) |
| Urinary tract infection | 3 (1.7) | 3 (2.2) |
| Pulmonary embolism | 1 (0.6) | 4 (2.9) |
| Dyspnea | 2 (1.1) | 2 (1.4) |
| Hematochezia | 1 (0.6) | 2 (1.4) |
| Acute coronary syndrome | 1 (0.6) | 2 (1.4) |
| Wound dehiscence | 1 (0.6) | 1 (0.7) |
| Unidentified infection | 0 (0) | 2 (1.4) |
| Ascites | 1 (0.6) | 0 (0) |
| Intra-abdominal abscess | 1 (0.6) | 0 (0) |
| Pressure ulcer | 1 (0.6) | 0 (0) |
| Disorientation | 1 (0.6) | 0 (0) |
| Supraventricular tachycardia | 1 (0.6) | 0 (0) |
| Allergic reaction | 1 (0.6) | 0 (0) |
| Urinary retention | 1 (0.6) | 0 (0) |
| Cardiac insufficiency | 1 (0.6) | 0 (0) |
| Diarrhea | 1 (0.6) | 0 (0) |
| Hyponatremia | 0 (0) | 1 (0.7) |
| Intestinal obstruction | 0 (0) | 1 (0.7) |
| Pleural effusion | 0 (0) | 1 (0.7) |
| Uterine infection | 0 (0) | 1 (0.7) |
Fig. 1Differences between the iv iron and control groups in all complications, Clavien-Dindo 1–2 complications, Clavien-Dindo 3–5 complications, and anemia at one month after surgery. A 95% confidence interval is shown using error bars