Association of pathologic factors with postoperative venous thromboembolism after gastrointestinal cancer surgery.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
934 patients who underwent GI cancer surgery, the incidence rates of 30-day postoperative VTE were 3.
I · Intervention 중재 / 시술
colorectal, pancreatic, primary hepatic, and esophageal cancer surgery between 2017 and 2020
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] Pathologic factors were associated with higher 30-day VTE risk after GI cancer surgery. Acknowledging the association of pathologic factors on VTE is an important first step to considering a more tailored approach to chemoprophylaxis.
[BACKGROUND] Venous thromboembolism (VTE) chemoprophylaxis is the standard of care after gastrointestinal (GI) cancer surgery; however, variation in risk based on pathologic factors (eg, stage and his
- p-value P < .05
- 95% CI 1.24-2.60
APA
Janczewski LM, Silver CM, et al. (2024). Association of pathologic factors with postoperative venous thromboembolism after gastrointestinal cancer surgery.. Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract, 28(6), 813-819. https://doi.org/10.1016/j.gassur.2024.03.002
MLA
Janczewski LM, et al.. "Association of pathologic factors with postoperative venous thromboembolism after gastrointestinal cancer surgery.." Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract, vol. 28, no. 6, 2024, pp. 813-819.
PMID
38553295 ↗
Abstract 한글 요약
[BACKGROUND] Venous thromboembolism (VTE) chemoprophylaxis is the standard of care after gastrointestinal (GI) cancer surgery; however, variation in risk based on pathologic factors (eg, stage and histology) is unclear. This study aimed to evaluate the association of pathologic factors with VTE after GI cancer surgery.
[METHODS] The American College of Surgeons National Surgical Quality Improvement Program procedure targeted datasets were queried for patients who underwent colorectal, pancreatic, primary hepatic, and esophageal cancer surgery between 2017 and 2020. Disease-specific and pathologic factors associated with postoperative VTE were evaluated using multivariable logistic regression.
[RESULTS] Among 70,934 patients who underwent GI cancer surgery, the incidence rates of 30-day postoperative VTE were 3.3% for pancreatic cancer, 3.2% for esophageal cancer, 2.7% for primary hepatic, and 1.3% for colorectal cancer. T stage was associated with VTE for colorectal cancer (T4 vs T1; odds ratio [OR], 1.79; 95% CI, 1.24-2.60), pancreatic cancer (all T stages vs T1; P < .05), and primary hepatic cancer (T4 vs T1; OR, 2.80; 95% CI, 1.55-5.08). N stage was associated with VTE for colorectal cancer (N2 vs N0; OR, 1.33; 95% CI, 1.04-1.68) and pancreatic cancer (N2 vs N0; OR, 1.36; 95% CI, 1.03-1.81). M stage was associated with VTE for colorectal cancer (OR, 1.47; 95% CI, 1.17-1.85) and esophageal cancer (OR, 2.54; 95% CI, 1.24-5.19). Histologic subtype was not associated with VTE, except for pancreatic neuroendocrine tumors vs adenocarcinoma (OR, 1.34; 95% CI, 1.03-1.74).
[CONCLUSION] Pathologic factors were associated with higher 30-day VTE risk after GI cancer surgery. Acknowledging the association of pathologic factors on VTE is an important first step to considering a more tailored approach to chemoprophylaxis.
[METHODS] The American College of Surgeons National Surgical Quality Improvement Program procedure targeted datasets were queried for patients who underwent colorectal, pancreatic, primary hepatic, and esophageal cancer surgery between 2017 and 2020. Disease-specific and pathologic factors associated with postoperative VTE were evaluated using multivariable logistic regression.
[RESULTS] Among 70,934 patients who underwent GI cancer surgery, the incidence rates of 30-day postoperative VTE were 3.3% for pancreatic cancer, 3.2% for esophageal cancer, 2.7% for primary hepatic, and 1.3% for colorectal cancer. T stage was associated with VTE for colorectal cancer (T4 vs T1; odds ratio [OR], 1.79; 95% CI, 1.24-2.60), pancreatic cancer (all T stages vs T1; P < .05), and primary hepatic cancer (T4 vs T1; OR, 2.80; 95% CI, 1.55-5.08). N stage was associated with VTE for colorectal cancer (N2 vs N0; OR, 1.33; 95% CI, 1.04-1.68) and pancreatic cancer (N2 vs N0; OR, 1.36; 95% CI, 1.03-1.81). M stage was associated with VTE for colorectal cancer (OR, 1.47; 95% CI, 1.17-1.85) and esophageal cancer (OR, 2.54; 95% CI, 1.24-5.19). Histologic subtype was not associated with VTE, except for pancreatic neuroendocrine tumors vs adenocarcinoma (OR, 1.34; 95% CI, 1.03-1.74).
[CONCLUSION] Pathologic factors were associated with higher 30-day VTE risk after GI cancer surgery. Acknowledging the association of pathologic factors on VTE is an important first step to considering a more tailored approach to chemoprophylaxis.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Venous Thromboembolism
- Female
- Male
- Postoperative Complications
- Middle Aged
- Aged
- Gastrointestinal Neoplasms
- Incidence
- Risk Factors
- Neoplasm Staging
- Digestive System Surgical Procedures
- Liver Neoplasms
- Esophageal Neoplasms
- Pancreatic Neoplasms
- Colorectal Neoplasms
- Retrospective Studies
- United States
- Gastrointestinal cancer
- Pathologic factors
- Venous thromboembolism
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