Abstract
Background
With the rising prevalence of abdominal radical hysterectomy, the need for perioperative blood transfusion has emerged as a significant clinical challenge. Independent risk factors for blood transfusion during abdominal radical hysterectomy remains limited, and identifying these factors is needed.
Methods
A retrospective analysis of data was performed using the Nationwide Inpatient Sample (NIS), focusing on patients who underwent abdominal radical hysterectomy between 2010 and 2019. Patients were categorized into two groups based on whether they received a blood transfusion. The analysis encompassed various demographic factors, including race, sex, and age, as well as length of stay (LOS), total hospitalization charges, hospital characteristics (admission type, insurance type, bed size, teaching status, geographic location, and hospital region), hospital mortality rates, comorbidities, and perioperative complications. Subsequently, both univariate and multivariate logistic regression analyses were employed to ascertain factors associated with abdominal radical hysterectomy patients requiring blood transfusions.
Results
Blood transfusions occurred in 14.84% of patients between 2010 and 2019, with a downward trend over time. Receiving a transfusion was associated with several negative outcomes, including a longer length of stay, higher total charges, and complications like thrombocytopenia, acute myocardial infarction, pneumonia, and so on. Additionally, patients who received transfusions were more likely to experience postoperative delirium, deep vein thrombosis, and wound infection. Independent risk factors for blood transfusion include Black race, Asian or Pacific Islander race, non-elective surgery, hospitalization in a rural setting, pre-existing medical conditions like coagulopathy, chronic blood loss anemia, deficiency anemia and others. Conversely, patients with private insurance, residing in the West, or Midwest/North Central regions were less likely to require a blood transfusion.
Conclusion
Our study highlights the concern of perioperative blood transfusion in radical hysterectomy, linked to significant complications. Reducing intraoperative blood loss and optimizing care based on patient factors are crucial for improving outcomes.
Supplementary Information
The online version contains supplementary material available at 10.1186/s12885-024-13216-3.
Keywords: Abdominal radical hysterectomy, Blood transfusion, Risk factor
Introduction
Approximately 14,000 individuals received a diagnosis of cervical cancer, resulting in 4,000 fatalities in US each year. Cervical cancer is one of the four most common and deadly cancers for women around the world [1]. For patients diagnosed with early-stage cervical cancer, the standard-of-care treatment approach often involves surgical removal of the uterus (radical hysterectomy) alongside the pelvic lymph nodes. This surgery can be performed traditionally through open surgery or by using minimally invasive techniques [2]. Following concerns raised by a 2018 randomized trial by Ramirez et al. [3]. suggesting a potential decrease in overall survival (OS) and disease-free survival (DFS) rates following minimally invasive surgery (MIS) for certain cancers, there has been a notable shift in practice within medical research centers worldwide. This shift is characterized by a resurgence in the use of open surgery [4–6]. The higher incidence of intraoperative hemorrhage and postoperative complications observed in open abdominal radical hysterectomy (ARH) compared to minimally invasive techniques warrant further investigation into the risk factors associated with perioperative blood transfusion during ARH, as well as other potential surgical complications [7–9].
Although blood transfusions are generally safe especially in developed countries due to strict blood screening, they can have some long-term and near-term complications, including acute or delayed hemolytic transfusion reactions, allergic reactions, alloimmunization, transfusion-related lung injury, and infection [10]. Blood transfusions may also cause slower functional recovery, a longer length of hospital stay, and more postoperative complications. Due to low donation rates, transfusion-transmitted infections, suboptimal management of blood stocks, and misallocation, blood for transfusion is an expensive and limited resource.
A recent study by Yang Shen compared intraoperative blood loss between ARH and MIS [11]. However, no prior studies have evaluated independent risk factors for blood transfusion following ARH. This investigation aimed to identify independent variables associated with an increased likelihood of blood transfusion after ARH.
Materials and methods
Database source
The Nationwide Inpatient Sample (NIS) stands as the most extensive all-payer database in the United States, capturing information on inpatient hospital stays [12]. This invaluable resource, sponsored by the Agency for Healthcare Research and Quality (AHRQ), compiles patient-level data from hospital discharges across participating states within the Healthcare Cost and Utilization Project (HCUP) [13]. The NIS offers a wealth of insights into healthcare utilization by including details such as hospitalization length, diagnoses, patient demographics, treatment received, and associated costs [14].
Data extraction
We analyzed data from the NIS database to conduct a retrospective study on women with invasive cervical cancer who underwent abdominal radical hysterectomy between 2010 and 2019. Cases were identified using specific diagnostic codes: ICD-9-CM 1800/1801/1808/1809 for cervical cancer and ICD-9-CM 6869 for ARH. The equivalent ICD-10-CM codes (C530/C531/C538/C539 for cancer and 0UB90ZZ/0UT90ZZ for ARH) were also employed. Since the NIS database is publicly available, as outlined in the Tri-Council Policy Statement (2010), obtaining institutional review board approval was not required. Notably, some patient characteristic data may have been missing from the database. We identified surgical complications using relevant ICD codes. A total of 3,188 unique patients were included in the final analysis. (Fig. 1)
Fig. 1.
Flowchart depicting the patient selection process based on the inclusion/exclusion criteria
Data analysis
The study cohort was divided into two groups based on whether they received a blood transfusion. Data extraction included complications, underlying comorbidities, demographics, and clinical outcomes. The presence of 29 distinct comorbidities was determined using the Agency for Healthcare Research and Quality Comorbidity Software, version 3.7, with these comorbidities flagged using ICD-10-CM and ICD-9-CM diagnosis codes.
To identify potential risk factors for blood transfusions after ARH this study employed a comprehensive statistical analysis. The Kolmogorov-Smirnov test was used to assess the normality of continuous variables. Continuous variables conforming to a normal distribution underwent Student’s t-tests, while non-parametric data were analyzed with the Mann-Whitney U test. Categorical variables were compared using the Chi-squared test. The Chi-square test was used to assess the association between each categorical variable and the outcome variable. Variables with P < 0.05 were selected into the multivariable analysis model. Additionally, variables have been identified as a risk factor for blood transfusion and socioeconomic factor (income level) were included in the regression models after adjusting for confounders [15] (Table 1). Approximately 10% of the data lacked information on patients’ race and ethnicity. To address these missing data and to mitigate the potential biases, we employed the method of multiple imputation. Complete case analysis was used in multivariate models. Hospital-level variables that were significantly associated with the occurrence of blood transfusion in the baseline data were used as stratification variables to further analyze transfusion-related risk factors. Given the limited number of rural hospitals, region of hospital was the sole stratification variable employed in the analysis. Possible interactions between covariates were considered as well. In addition, we performed propensity score matching (PSM) for several socioeconomic factors, including teaching status of hospital, location of hospital, type of insurance, region of the hospital and income level, to reduce potential confounding biases in our analysis. A 2-sided P < 0.05 was considered statistically significant. Statistical analyses were performed using the SPSS Statistics 26.0.
Table 1.
Variables used in binary logistic regression analysis
| Variable categories | Specific variables |
|---|---|
| Patient demographics | Age (≤ 60 years and>60 years), sex (male and female), race (White, Black, Hispanic, Asian or Pacific Islander, Native American and Other), income level (Lowest quartile, second quartile, third quartile, highest quartile) |
| Hospital characteristics | Type of admission (non-elective, elective), teaching status of hospital (nonteaching, teaching), location of hospital (rural, urban), type of insurance (Medicare, Medicaid, private insurance, self-pay, no charge, other), region of the hospital (northeast, Midwest or north central, south, west) |
| Comorbidities | AIDS, alcohol abuse, deficiency anemia, rheumatoid diseases, chronic blood loss anemia, congestive heart failure, chronic pulmonary disease, coagulopathy, depression, diabetes (uncomplicated), diabetes (with chronic complications), drug abuse, hypertension, hypothyroidism, liver disease, lymphoma, fluid and electrolyte disorders, metastatic cancer, neurological disorders, obesity, paralysis, peripheral vascular disorders, psychoses, pulmonary circulation disorders, renal failure, solid tumor without metastasis, peptic ulcer disease, valvular disease and weight loss |
Result
This study analyzed data from the NIS database to investigate blood transfusion rates following abdominal radical hysterectomy for invasive cervical cancer patients. Over a ten-year period (2010–2019), 50,133 patients with invasive cervical cancer were identified. Among these patients, 3,284 underwent ARH surgery. After excluding patients with missing data (96), a total of 3,188 patients were included in the final analysis. Within this group, 473 patients received blood transfusions, resulting in an overall transfusion rate of 14.84%. Figure 2 depicts the annual trends for both ARH procedures and blood transfusion rates over the course of the study period.
Fig. 2.
Annual cases of abdominal radical hysterectomy and incidence of blood transfusion (2010–2019)
Analysis of patient characteristics revealed several factors associated with blood transfusions. Patients who received transfusions were significantly older (P = 0.005) and remained hospitalized for a longer duration (LOS) (P < 0.001), incurring higher total charges (TOTCHG) (P < 0.001) compared to those who did not. Additionally, factors such as Black or Asian/Pacific Islander race (OR 1.525, 95%CI: 1.134–2.051, P = 0.005; OR 2.135, 95%CI: 1.413–3.226, P < 0.001, respectively), non-elective surgery (P < 0.001), and treatment at a rural hospital (P = 0.014) were associated with an increased likelihood of blood transfusion. Conversely, patients with private insurance (P < 0.001) and those residing in the West (OR 0.674, 95%CI: 0.485–0.937, P = 0.019) or Midwest/North Central regions (OR 0.689, 95%CI: 0.485–0.980, P = 0.038) were less likely to require blood transfusions. While the blood transfusion group exhibited a higher mortality rate, the difference did not reach statistical significance (P = 0.220). (Tables 2 and 3)
Table 2.
Patient characteristics and outcomes after abdominal radical hysterectomy (2010–2019)
| Characteristics | Transfusion | No Transfusion | P | |
|---|---|---|---|---|
| Total (n = count) | 473 | 2,715 | ||
| Total incidence | 14.84% | |||
| Age (median, IQR, years) | 48 (40–60) | 47 (38–57) | 0.005 | |
| Age group | ||||
| ≤ 60 | 362(76.2%) | 2198(81.0%) | 0.015 | |
| > 60 | 113(23.8%) | 515(19.0%) | ||
| Race | ||||
| White | 235(49.5%) | 1554(57.3%) | < 0.001 | |
| Black | 81(17.1%) | 320(11.8%) | ||
| Hispanic | 82(17.3%) | 473(17.4%) | ||
| Asian or Pacific Islander | 39(8.2%) | 125(4.6%) | ||
| Native American | 14(2.9%) | 135(5.0%) | ||
| Other | 24(5.1%) | 106(3.9%) | ||
| LOS (median, IQR, days) | 5 (4–7) | 3 (2–4) | < 0.001 | |
| TOTCHG (median, IQR, $) | 68,972(44,005-107,917.5) | 48,287(33,220 − 73,577) | < 0.001 | |
| Type of insurance | ||||
| Medicare | 86(13.3%) | 363(18.0%) | < 0.001 | |
| Medicaid | 143(26.7%) | 726(30.2%) | ||
| Private insurance | 189(50.9%) | 1378(39.7%) | ||
| Self-pay | 28(4.2%) | 115(5.9%) | ||
| No charge | 4(1.2%) | 33(0.8%) | ||
| Other | 25(3.6%) | 98(5.3%) | ||
| Bed size of hospital | ||||
| Small | 32(6.7%) | 234(8.6%) | 0.383 | |
| Medium | 102(21.5%) | 561(20.7%) | ||
| Large | 341(71.8%) | 1918(70.7%) | ||
| Elective admission | 2449(90.3%) | 386(81.3%) | < 0.001 | |
| Type of hospital (teaching ) | 2331(85.9%) | 409(86.1%) | 0.914 | |
| Location of hospital (urban) | 1(0.2%) | 46(1.7%) | 0.013 | |
| Region of hospital | ||||
| Northeast | 92(19.4%) | 408(15.0%) | 0.006 | |
| Midwest or North Central | 78(16.4%) | 587(21.6%) | ||
| South | 202(42.5%) | 1059(39.0%) | ||
| West | 103(21.7%) | 659(24.3%) | ||
| Died | 2(0.4%) | 4(0.1%) | 0.204 | |
| Income level | ||||
| Lowest quartile | 132(28.4%) | 784(29.5%) | 0.617 | |
| Second quartile | 107(23.0%) | 661(24.9%) | ||
| Third quartile | 119(25.6%) | 664(25.0%) | ||
| Highest quartile | 107(23.0%) | 550(20.7%) | ||
LOS: Length of stay, TOTCHE: Total charge
Table 3.
Risk factors associated with blood transfusion after abdominal radical hysterectomy
| Variable | Multivariate Logistic Regression | |||
|---|---|---|---|---|
| OR | 95% CI | P | ||
| Age > 60 years old | 1.101 | 0.815–1.486 | 0.531 | |
| Race | ||||
| White | Ref | —— | —— | |
| Black | 1.525 | 1.134–2.051 | 0.005 | |
| Hispanic | 1.119 | 0.834–1.501 | 0.455 | |
| Asian or Pacific Islander | 2.135 | 1.413–3.226 | <0.001 | |
| Native American | 0.800 | 0.442–1.451 | 0.463 | |
| Other | 1.207 | 0.736–1.98 | 0.456 | |
| Type of insurance | ||||
| Medicare | Ref | —— | —— | |
| Medicaid | 0.881 | 0.609–1.275 | 0.502 | |
| Private insurance | 0.637 | 0.448–0.906 | 0.012 | |
| Self-pay | 1.001 | 0.583–1.719 | 0.996 | |
| No charge | 0.589 | 0.196–1.77 | 0.346 | |
| Other | 1.197 | 0.695–2.06 | 0.516 | |
| Income level | ||||
| Lowest quartile | Ref | —— | —— | |
| Second quartile | 1.043 | 0.785–1.385 | 0.773 | |
| Third quartile | 1.173 | 0.885–1.555 | 0.267 | |
| Highest quartile | 1.334 | 0.986–1.805 | 0.061 | |
| Elective admission | 0.504 | 0.383–0.662 | <0.001 | |
| Teaching hospital | 0.520 | 0.400–0.690 | 0.623 | |
| Region of hospital | ||||
| Northeast | Ref | —— | —— | |
| Midwest or North Central | 0.689 | 0.485–0.980 | 0.038 | |
| South | 0.920 | 0.691–1.226 | 0.570 | |
| West | 0.674 | 0.485–0.937 | 0.019 | |
OR: Odds ratio, CI: Confidence interval
The following covariates were controlled: age, race, primary payer, admission type, hospital teaching status, hospital region
Preoperative comorbidities significantly influenced blood transfusion rates. Patients with conditions like coagulopathy (OR 4.33, 95%CI: 2.62–7.15, P < 0.001), chronic blood loss anemia (OR 4.29, 95%CI: 2.64–6.99, P < 0.001), and deficiency anemia (OR 3.95, 95%CI: 2.88–5.42, P < 0.001) were at a considerably higher risk. Similarly, other comorbidities such as fluid and electrolyte disorders (OR 1.94, 95%CI: 1.42–2.64, P < 0.001), peripheral vascular disorders (OR 2.72, 95%CI: 1.32–5.63, P = 0.007), and pulmonary circulation disorders (OR 3.33, 95%CI: 1.05–10.57, P = 0.041) were associated with increased transfusion risk. Additionally, statistically significant differences in blood transfusion rates were observed between groups based on the presence of hypertension (P = 0.001), renal failure (P = 0.001), weight loss (P = 0.001), paralysis (P = 0.015), and congestive heart failure (P = 0.023). (Table 4).
Table 4.
Relationship between blood transfusion and preoperative comorbidities
| Comorbidities | Univariate Analysis | Multivariate Logistic Regression | |||||
|---|---|---|---|---|---|---|---|
| No transfusion | Transfusion | P | OR | 95% CI | P | ||
| Preoperative comorbidities | |||||||
| Coagulopathy | 45 (1.7%) | 37 (7.8%) | < 0.001 | 4.33 | 2.62–7.15 | <0.001 | |
| Chronic blood loss anemia | 47 (1.7%) | 33 (7.0%) | < 0.001 | 4.29 | 2.64–6.99 | <0.001 | |
| Deficiency anemia | 129 (4.8%) | 83 (17.5%) | < 0.001 | 3.95 | 2.88–5.42 | <0.001 | |
| Fluid and electrolyte disorders | 216 (8.0%) | 91 (19.2%) | < 0.001 | 1.94 | 1.42–2.64 | <0.001 | |
| Peripheral vascular disorders | 26 (1.0%) | 13 (2.7%) | 0.001 | 2.72 | 1.32–5.63 | 0.007 | |
| Pulmonary circulation disorders | 9 (0.3%) | 7 (1.5%) | 0.004 | 3.33 | 1.05–10.57 | 0.041 | |
| Diabetes (with chronic complications) | 44 (1.6%) | 16 (3.4%) | 0.009 | 1.95 | 1.01–3.74 | 0.046 | |
| Renal failure | 43 (1.6%) | 18 (3.8%) | 0.001 | 1.31 | 0.68–2.54 | 0.417 | |
| Weight loss | 62 (2.3%) | 24 (5.1%) | 0.001 | 1.18 | 0.68–2.06 | 0.561 | |
| Hypertension | 761 (28.0%) | 167 (35.3%) | 0.001 | 1.17 | 0.92–1.49 | 0.202 | |
| Paralysis | 6 (0.2%) | 5 (1.1%) | 0.015 | 2.58 | 0.68–9.80 | 0.164 | |
| Congestive heart failure | 23 (0.8%) | 10 (2.1%) | 0.023 | 0.85 | 0.33–2.16 | 0.724 | |
| Acquired immune deficiency syndrome | 10 (0.4%) | 2 (0.4%) | 0.860 | 1.06 | 0.21–5.34 | 0.947 | |
| Chronic pulmonary disease | 279 (10.3%) | 58 (12.3%) | 0.195 | 1.00 | 0.72–1.40 | 0.981 | |
| Depression | 282 (10.4%) | 47 (9.9%) | 0.766 | 0.93 | 0.65–1.31 | 0.664 | |
| Diabetes, uncomplicated | 218 (8.0%) | 50 (10.6%) | 0.066 | 1.22 | 0.85–1.76 | 0.283 | |
| Drug abuse | 47 (1.7%) | 12 (2.5%) | 0.230 | 1.19 | 0.59–2.39 | 0.633 | |
| Hypothyroidism | 219 (8.1%) | 32 (6.8%) | 0.332 | 0.74 | 0.49–1.13 | 0.160 | |
| Liver disease | 45 (1.7%) | 8 (1.7%) | 0.958 | 0.55 | 0.23–1.31 | 0.177 | |
| Rheumatoid arthritis/collagen vascular diseases | 32 (1.2%) | 5 (1.1%) | 0.820 | 0.84 | 0.31–2.30 | 0.737 | |
| Alcohol abuse | 23 (0.8%) | 9 (1.9%) | 0.061 | 1.80 | 0.75–4.35 | 0.191 | |
| Neurological disorders | 31 (1.1%) | 9 (1.9%) | 0.170 | 1.08 | 0.47–2.49 | 0.852 | |
| Obesity | 441 (16.2%) | 84 (17.8%) | 0.412 | 1.01 | 0.76–1.34 | 0.948 | |
| Psychoses | 66 (2.4%) | 18 (3.8%) | 0.085 | 1.65 | 0.92–2.98 | 0.094 | |
| Valvular disease | 26 (1.0%) | 9 (1.9%) | 0.069 | 1.66 | 0.68–4.05 | 0.263 | |
AIDS: Acquired immunodeficiency syndrome, OR: Odds ratio, CI: Confidence interval
Multivariate analysis revealed a significant association between blood transfusion during ARH. Compared to those who did not receive a transfusion, these patients had a 3.25-fold higher likelihood of thrombocytopenia (OR 3.25, 95%CI: 1.78–5.96, P < 0.001) and a 9.13-fold likelihood of AMI (OR 9.13, 95%CI: 2.97–27.94, P < 0.001).
Perioperative blood transfusion was also independently associated pneumonia (OR 3.56, 95%CI: 1.76–7.17, P < 0.001), urinary tract infection (OR 2.05, 95%CI: 1.21–3.47, P = 0.008), postoperative delirium (OR 10.17, 95%CI: 1.78–57.97, P = 0.009), DVT (OR 2.64, 95%CI: 1.03–6.80, P = 0.044), and wound infection (OR 2.62, 95%CI: 1.23–5.62, P = 0.013) (Table 5).
Table 5.
Relationship between blood transfusion and postoperative complications
| Complications | Univariate Analysis | Multivariate Logistic Regression | |||||
|---|---|---|---|---|---|---|---|
| No transfusion | Transfusion | P | OR | 95% CI | P | ||
| Medical complications | |||||||
| Hemorrhage | 23 (0.8%) | 26 (5.5%) | < 0.001 | 5.21 | 2.77–9.80 | <0.001 | |
| Thrombocytopenia | 33 (1.2%) | 22 (4.7%) | < 0.001 | 3.25 | 1.78–5.96 | <0.001 | |
| AMI | 5 (0.2%) | 12 (2.5%) | < 0.001 | 9.13 | 2.97–27.94 | <0.001 | |
| Pneumonia | 21 (0.8%) | 21 (4.4%) | < 0.001 | 3.56 | 1.76–7.17 | < 0.001 | |
| Urinary tract infection | 77 (2.8%) | 46 (9.7%) | < 0.001 | 2.05 | 1.21–3.47 | 0.008 | |
| Postoperative delirium | 2 (0.1%) | 5 (1.1%) | < 0.001 | 10.17 | 1.78–57.97 | 0.009 | |
| DVT | 13 (0.5%) | 10 (2.1%) | < 0.001 | 2.64 | 1.03–6.80 | 0.044 | |
| Genitourinary disease | 147 (5.4%) | 69 (14.6%) | < 0.001 | 1.54 | 0.87–2.73 | 0.139 | |
| Acute renal failure | 74 (2.7%) | 37 (7.8%) | < 0.001 | 1.15 | 0.58–2.31 | 0.688 | |
| Gastrointestinal complication | 53 (2.0%) | 22 (4.7%) | < 0.001 | 1.70 | 0.95–3.03 | 0.072 | |
| Convulsion | 4 (0.1%) | 2 (0.4%) | 0.258 | 2.51 | 0.42–15.17 | 0.316 | |
| PE | 15 (0.6%) | 6 (1.3%) | 0.142 | 1.29 | 0.43–3.87 | 0.649 | |
| Respiratory disease | 19 (0.7%) | 9 (1.9%) | 0.020 | 1.20 | 0.47–3.06 | 0.706 | |
| Septicemia | 27 (1.0%) | 19 (4.0%) | < 0.001 | 0.96 | 0.44–2.11 | 0.917 | |
| GI bleeding | 3 (0.1%) | 1 (0.2%) | 0.474 | 0.10 | 0.00-4.67 | 0.240 | |
| Chest pain | 14 (0.5%) | 1 (0.2%) | 0.597 | 0.21 | 0.02–1.91 | 0.164 | |
| Urinary retention | 76 (2.8%) | 14 (3.0%) | 0.846 | 0.95 | 0.52–1.75 | 0.875 | |
| Respiratory failure | 10 (0.4%) | 8 (1.7%) | 0.001 | 1.53 | 0.48–4.86 | 0.467 | |
| Continuous trauma ventilation | 8 (0.3%) | 8 (1.7%) | < 0.001 | 2.11 | 0.62–7.16 | 0.230 | |
| Arrhythmia | 4 (0.1%) | 2 (0.4%) | 0.220 | 3.39 | 0.61–18.89 | 0.164 | |
| Heart failure | 14 (0.5%) | 9 (1.9%) | 0.030 | 1.74 | 0.64–4.73 | 0.277 | |
| Cardiac arrest | 5 (0.2%) | 4 (0.8%) | 0.042 | 2.08 | 0.36–12.22 | 0.416 | |
| Postoperative shock | 4 (0.1%) | 5 (1.1%) | 0.382 | 1.66 | 0.34–8.02 | 0.582 | |
| Surgical complications | |||||||
| Wound infection | 18 (0.7%) | 16 (3.4%) | < 0.001 | 2.62 | 1.23–5.62 | 0.013 | |
| Surgical incision dehiscence | 8 (0.3%) | 10 (2.1%) | < 0.001 | 2.52 | 0.83–7.69 | 0.103 | |
| Urinary tract injury | 4 (0.1%) | 2 (0.4%) | 0.220 | 3.19 | 0.56–18.33 | 0.193 | |
| Lower limb peripheral nerve injuries | 16 (0.6%) | 6 (1.3%) | 0.178 | 2.01 | 0.73–5.58 | 0.178 | |
OR: Odds ratio, CI: Confidence interval, DVT: Deep vein thrombosis, PE: pulmonary embolism, AMI: Acute myocardial infarction, GI bleeding: Gastrointestinal bleeding
We also conducted region of hospital-stratified regression analyses to further identify the possible risk factors for blood transfusion. Notably, non-elective surgery emerged as a significant predictor of blood transfusion in most regions, except in the West hospital (Supplementary Fig. 3). Also, in the Northeast region, the initial logistic regression model, devoid of interaction terms, indicated that black patients were more likely to undergo blood transfusions compared to their white counterparts (P = 0.007). Also, in the northern region after considering the interaction between race and payment type there is no significant difference between the black and the white (P = 0.054).(Fig. 3).
Fig. 3.
Risk factors associated with blood transfusion after abdominal radical hysterectomy in Northeast
After PSM, the Black people is no longer a significant risk factor(P = 0.136). (Supplementary Table 5)
Discussion
In the United States alone, an estimated 13,960 individuals receive a cervical cancer diagnosis annually, with approximately 4,310 succumbing to the disease in 2023 [16]. Treatment for cervical cancer is primarily determined by the stage of the cancer and often involves a combination of chemoradiation and surgery, or surgery alone. And since 2018, several studies have suggested that minimally invasive surgery may be associated with lower DFS and OS rates, along with a higher risk of recurrence compared to the traditional open surgical approach [3, 17]. This has led to a widespread adoption of ARH in recent years. Consequently, this study was aimed at exploring the incidence and possible factors associated with ARH.
In this study, 473 patients (14.84%) received blood transfusions during perioperative period. Notably, blood transfusion rates exhibited a declining trend, decreasing from 18.83% in 2010 to 9.76% in 2019 (Fig. 2). The transfusion rate during ARH identified in this study was higher than that reported in another study, which documented a blood transfusion incidence of 10.7% [18]. This discrepancy is likely due to differences in the data collection period, as the surgical techniques and clinical guidelines may have evolved between these periods [18]. As expected, the blood transfusion rates in the ARH group substantially exceeded the rate in the minimally invasive surgery group, consistent with findings from other studies [15, 18, 19]. However, the mortality rate among patients who received transfusions during ARH was not significantly different from that reported laparoscopic surgery transfusion, suggesting that transfusions themselves may not be the primary driver of mortality differences between these approaches [15]. Additionally, a study published in 2021 found that the incidences of any single complication, intraoperative complications, and postoperative complications were higher in the LRH group compared to the ARH group [19].
Furthermore, limited research has investigated the predictors of blood transfusion for this patient population [20]. Our comprehensive analysis, spanning the years 2010 to 2019, examines both the economic and healthcare implications of perioperative blood transfusion in ARH. We employed logistic regression analysis to explore the association between hospital characteristics, demographic variables, and the likelihood of blood transfusion. As highlighted previously, our study identified a higher likelihood of blood transfusion among patients of Asian, Pacific Islander, or Black descent. This may be attributable to the documented high proportion of anemics within these populations [21]. Interestingly, an increased propensity for administering blood transfusions was observed in rural hospitals located in the Northeastern region of the United States. This phenomenon may be attributed to several factors, including disparities in available medical technology, variations in institutional protocols, and adherence to differing transfusion standards. Specifically, the criteria utilized to determine the necessity for transfusions in this region may play a crucial role in influencing transfusion practices [15, 22, 23].
Furthermore, patients with private insurance may exhibit a higher socioeconomic status and potentially healthier baseline profiles [24, 25]. This could translate to a lower prevalence of conditions like coagulopathy, chronic blood loss anemia, and nutritional deficiencies, consequently reducing the need for blood transfusions. Additionally, our findings suggest that elderly patients are more susceptible to requiring blood transfusion. This could be due to their reduced tolerance for blood loss and a higher burden of cardiovascular comorbidities [26].
It is now understood that several underlying health conditions significantly elevate a patient’s need for blood transfusions. These conditions, often characterized by diminished hemoglobin levels and increased bleeding risks, include coagulopathies, chronic and deficiency anemias, and fluid and electrolyte imbalances. Extensive data analysis supports this link, suggesting that blood loss, hemorrhages, shock, and gastrointestinal bleeding can all contribute to these imbalances and necessitate transfusions [27].
Our study further identified patients with peripheral vascular disorders, and pulmonary circulation disorders as at-risk groups. Chronic complications of diabetes can also increase transfusion risk. These conditions likely elevate transfusion needs due to a combination of factors, including changes in blood vessel permeability, iron or protein deficiency anemia, and nutrient depletion associated with chronic illness [28, 29].
Research indicates significant correlations between certain underlying health conditions and patients’ need for blood transfusions. These conditions are typically associated with reduced hemoglobin levels and increased bleeding tendencies, including coagulation disorders, chronic and deficiency anemias, and fluid and electrolyte imbalances. Extensive data analysis supports this association, suggesting that blood loss, hemorrhage, shock, and gastrointestinal bleeding may all be linked to these imbalanced states and transfusion requirements [28].
Our study also found that patients with peripheral vascular disease, and pulmonary circulation disorders may exhibit higher correlations with transfusion needs. Chronic complications of diabetes also demonstrated correlations with transfusion requirements. The association of these conditions with transfusion needs may involve multiple factors, including alterations in vascular permeability, iron or protein deficiency anemias, and nutritional depletion associated with chronic illnesses.
Our study observed that in certain regions, black patients were more likely than white patients to receive blood transfusions, but this difference was no longer significant after considering the interaction between race and payment type. This may reflect the complex relationship between race and socioeconomic status [30, 31]. On one hand, different payment types may represent varying economic levels and access to medical services among patients, potentially influencing physicians’ decisions regarding blood transfusion. On the other hand, racial disparities might be associated with unequal distribution of medical resources, differences in quality and access to healthcare services [32]. Research indicates that disparities in cervical cancer rates and outcomes are attributed to unequal access to healthcare services and the insufficient awareness, knowledge, and perceived susceptibility to HPV and cervical cancer among vulnerable women. It is crucial to advocate for preventive measures across the broader population, particularly for vulnerable groups, as such initiatives can not only reduce the incidence of complications and comorbidities but also lower the rates of cervical cancer itself.
This study has several limitations inherent to research using large administrative databases. The NIS primarily captures healthcare utilization data, lacking clinically relevant details such as cervical cancer stage, blood loss, transfusion amounts, anesthesia types, and perioperative hemoglobin levels [19]. Thus, a prospective cohort study is needed to further identify the potential relationship between the blood transfusion and other complications. Although this limits the depth of clinical analysis, it does not impede the identification of risk factors. A key strength of the NIS is its large sample size, which strengthens the findings and offers valuable insights for managing invasive cervical cancer patients undergoing ARH. Additionally, the NIS focuses on hospitalization data, omitting long-term post-discharge complications [12]. This limits our ability to track outcomes beyond the inpatient stay. Coding inaccuracies or omissions related to complications and transfusions may also affect the results, emphasizing the need for accurate coding practices. Finally, as with any observational study, unmeasured confounding factors may influence outcomes. However, the large sample size helps mitigate potential biases.
Conclusion
Our study underscores the increasing challenge of perioperative blood transfusion in radical hysterectomy, particularly with the rise in open surgeries. Blood transfusion was associated with significant postoperative complications, emphasizing the need for gynecologic oncologists to adopt strategies that minimize intraoperative blood loss. Key patient factors, such as race, insurance type, and pre-existing health conditions, should guide preoperative optimization to improve outcomes and reduce unnecessary complications.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Supplementary Figures: Supplementary Figure 1: Risk factors associated with blood transfusion after abdominal radical hysterectomy in Midwest or North Central. Supplementary Figure 2: Risk factors associated with blood transfusion after abdominal radical hysterectomy in South. Supplementary Figure 3: Risk factors associated with blood transfusion after abdominal radical hysterectomy in West
Supplementary Tables: Supplementary Table 1: Patient characteristics and outcomes after abdominal radical hysterectomy in Northeast (2010–2019). Supplementary Table 2: Patient characteristics and outcomes after abdominal radical hysterectomy in Midwest or North Central (2010–2019). Supplementary Table 3: Patient characteristics and outcomes after abdominal radical hysterectomy in South (2010–2019). Supplementary Table 4: Patient characteristics and outcomes after abdominal radical hysterectomy in West (2010–2019). Supplementary table 5: Risk factors associated with blood transfusion after abdominal radical hysterectomy in the PSM-matched cohort
Acknowledgements
None.
Author contributions
Chuan Chen: Formal analysis, Writing – original draft, Writing – review & editing; BenLi Zhu: Data curation, Writing – original draft, Writing – review & editing; YouFeng Wang: Data curation, Writing – original draft; YangYang Zhao: Figurse and tables design; Gang Chen: Conceptualization, Project administration; Ying Peng: Conceptualization, Methodology; Ying2 Peng: Data curation, Investigation, Resources, Software; XinYu Wang: Conceptualization, Resources, Software; Hao Xie: Methodology, Supervision, Validation; Ying Zhou: Conceptualization, Supervision, Validation, Visualization; Juan Lin: Methodology, Supervision, Validation, Visualization, Revision.
Funding
This work was supported by Guangzhou Science and Technology Plan Project, Number 2023A04J0624.
Data availability
The datasets are available at https://www.ahrq.gov/data/hcup/index.html.
Declarations
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Chuan Chen, BenLi Zhu and Youfeng Wang contributed equally to this work.
Contributor Information
Hao Xie, Email: hao_xie2018@163.com.
Ying Zhou, Email: caddiezy@ustc.edu.cn.
Juan Lin, Email: linpyk@163.com.
References
- 1.Perkins RB, Wentzensen N, Guido RS, Schiffman M. Cervical Cancer screening: a review. JAMA 2023;330. 10.1001/jama.2023.13174 [DOI] [PubMed]
- 2.Abu-Rustum NR, Yashar CM, Bean S, Bradley K, Campos SM, Chon HS, et al. NCCN guidelines insights: Cervical Cancer, Version 1.2020. J Natl Compr Cancer Netw. 2020;18. 10.6004/jnccn.2020.0027 [DOI] [PubMed]
- 3.Ramirez PT, Frumovitz M, Pareja R, Lopez A, Vieira M, Ribeiro R, et al. Minimally invasive versus Abdominal Radical Hysterectomy for Cervical Cancer. N Engl J Med. 2018;379. 10.1056/nejmoa1806395 [DOI] [PubMed]
- 4.Piedimonte S, Pond GR, Plante M, Nelson G, Kwon J, Altman A, et al. Comparison of outcomes between abdominal, minimally invasive and combined vaginal-laparoscopic hysterectomy in patients with stage IAI/IA2 cervical cancer: 4 C (Canadian Cervical Cancer Collaborative) study. Gynecol Oncol. 2022;166. 10.1016/j.ygyno.2022.05.011 [DOI] [PubMed]
- 5.Hayek J, Mowzoon M, Demissie S, Palileo A, Serur E, Goldberg GL, et al. Minimally invasive versus open surgery for women with stage 1A1 and stage 1A2 cervical cancer: a retrospective database cohort study. Ann Med Surg. 2022;77:103507. 10.1016/j.amsu.2022.103507 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Basaran D, Leitao MM. The Landmark Series: minimally invasive surgery for cervical Cancer. Ann Surg Oncol. 2021;28. 10.1245/s10434-020-09265-0 [DOI] [PMC free article] [PubMed]
- 7.Cao T, Feng Y, Huang Q, Wan T, Liu J. Prognostic and Safety roles in Laparoscopic Versus Abdominal Radical Hysterectomy in Cervical Cancer: a Meta-analysis. J Laparoendosc Adv Surg Tech. 2015;25. 10.1089/lap.2015.0390 [DOI] [PMC free article] [PubMed]
- 8.Wang Yzhou, Deng L, Xu Hcheng, Zhang Y, Liang Zqing. Laparoscopy versus laparotomy for the management of early stage cervical cancer. BMC Cancer. 2015;15. 10.1186/s12885-015-1818-4 [DOI] [PMC free article] [PubMed]
- 9.Zhao Y, Hang B, Xiong GW, Zhang XW. Laparoscopic radical hysterectomy in early stage cervical cancer: a systematic review and meta-analysis. J Laparoendosc Adv Surg Tech. 2017;27. 10.1089/lap.2017.0022 [DOI] [PubMed]
- 10.Blanco JF, Díaz A, Melchor FR, da Casa C, Pescador D. Risk factors for periprosthetic joint infection after total knee arthroplasty. Arch Orthop Trauma Surg. 2020;140. 10.1007/s00402-019-03304-6 [DOI] [PubMed]
- 11.Lv X, Ding B, Xu JY, Shen Y. Effect of modified radical laparoscopic hysterectomy versus open radical hysterectomy on short-term clinical outcomes in early-stage cervical cancer: a single-center, prospective, randomized controlled trial. World J Surg Oncol. 2023;21. 10.1186/s12957-023-03044-3 [DOI] [PMC free article] [PubMed]
- 12.Masoomi H, Blumenauer BJ, Blakkolb CL, Marques ES, Greives MR. Predictors of blood transfusion in autologous breast reconstruction surgery: a retrospective study using the nationwide inpatient sample database. J Plast Reconstr Aesthetic Surg. 2019;72. 10.1016/j.bjps.2019.06.012 [DOI] [PubMed]
- 13.Stulberg JJ, Haut ER. Practical guide to surgical data sets: Healthcare cost and utilization project National Inpatient Sample (NIS). JAMA Surg. 2018;153. 10.1001/jamasurg.2018.0542 [DOI] [PubMed]
- 14.Zakhari A, Czuzoj-Shulman N, Spence AR, Gotlieb WH, Abenhaim HA. Laparoscopic and robot-assisted hysterectomy for uterine cancer: a comparison of costs and complications. Am J Obstet Gynecol. 2015;213. 10.1016/j.ajog.2015.07.004 [DOI] [PubMed]
- 15.Cao X, Liu X, Zhang X, Zhang K, Chen C, Yang Q et al. Risk factors for perioperative blood transfusion in patients undergoing total laparoscopic hysterectomy. BMC Womens Health 2024;24. 10.1186/s12905-024-02908-4 [DOI] [PMC free article] [PubMed]
- 16.Siegel RL, Miller KD, Wagle NS, Jemal A. Cancer statistics, 2023. CA Cancer J Clin. 2023;73. 10.3322/caac.21763 [DOI] [PubMed]
- 17.Melamed A, Margul DJ, Chen L, Keating NL, del Carmen MG, Yang J, et al. Survival after minimally invasive radical hysterectomy for early-stage cervical Cancer. N Engl J Med. 2018;379. 10.1056/nejmoa1804923 [DOI] [PMC free article] [PubMed]
- 18.Schivardi G, Casarin J, Habermann EB, Bews KA, Langstraat CL, Cliby W, et al. Practice patterns and complications of hysterectomy for invasive cervical cancer after the Laparoscopic Approach to Cervical Cancer trial. Am J Obstet Gynecol. 2024;230. 10.1016/j.ajog.2023.09.002 [DOI] [PubMed]
- 19.Li Z, Chen C, Liu P, Duan H, Liu M, Xu Y, et al. Comparison of oncological outcomes and major complications between laparoscopic radical hysterectomy and abdominal radical hysterectomy for stage IB1 cervical cancer with a tumour size less than 2 cm. Eur J Surg Oncol. 2021;47. 10.1016/j.ejso.2021.03.238 [DOI] [PubMed]
- 20.Sim JH, Jang DM, Cho HS, Park JY, Choi WJ. Association of Red Cell distribution width/ albumin ratio with intraoperative blood transfusion in cervical cancer patients. PLoS ONE. 2022;17. 10.1371/journal.pone.0277481 [DOI] [PMC free article] [PubMed]
- 21.Shaz BH, Zimring JC, Demmons DG, Hillyer CD. Blood donation and blood transfusion: Special considerations for African americans. Transfus Med Rev. 2008;22. 10.1016/j.tmrv.2008.02.006 [DOI] [PubMed]
- 22.Goel R, Patel EU, White JL, Chappidi MR, Ness PM, Cushing MM et al. Factors associated with red blood cell, platelet, and plasma transfusions among inpatient hospitalizations: a nationally representative study in the United States. Transfusion 2019;59. 10.1111/trf.15088 [DOI] [PMC free article] [PubMed]
- 23.Saleh A, Small T, Pillai ALPC, Schiltz NK, Klika AK, Barsoum WK. Allogenic blood transfusion following total hip arthroplasty: results from the nationwide inpatient sample, 2000 to 2009. J Bone Jt Surg - Am 2014;96. 10.2106/JBJS.M.00825 [DOI] [PMC free article] [PubMed]
- 24.Akinyemiju T, Meng Q, Vin-Raviv N. Race/ethnicity and socio-economic differences in colorectal cancer surgery outcomes: analysis of the nationwide inpatient sample. BMC Cancer. 2016;16. 10.1186/s12885-016-2738-7 [DOI] [PMC free article] [PubMed]
- 25.Rambiritch V, Verburgh E, Louw VJ. Patient blood management and blood conservation – complimentary concepts and solutions for blood establishments and clinical services in South Africa and beyond. Transfus Apher Sci. 2021;60. 10.1016/j.transci.2021.103207 [DOI] [PMC free article] [PubMed]
- 26.Ad N, Massimiano PS, Burton NA, Halpin L, Pritchard G, Shuman DJ, et al. Effect of patient age on blood product transfusion after cardiac surgery. J Thorac Cardiovasc Surg. 2015;150. 10.1016/j.jtcvs.2015.03.022 [DOI] [PubMed]
- 27.Saad-Naguib M, Ulker A, Timmons D, Grady M, Lederer M, Carugno J. Risk factors for perioperative blood transfusion in patients undergoing hysterectomy for benign disease in a teaching institution. Arch Gynecol Obstet. 2022;305. 10.1007/s00404-021-06223-3 [DOI] [PubMed]
- 28.Murji A, Lam M, Allen B, Richard L, Shariff SZ, Austin PC et al. Risks of preoperative anemia in women undergoing elective hysterectomy and myomectomy. Am J Obstet Gynecol 2019;221. 10.1016/j.ajog.2019.07.018 [DOI] [PubMed]
- 29.Masoomi H, Rimler J, Wirth GA, Lee C, Paydar KZ, Evans GRD. Frequency and risk factors of blood transfusion in Abdominoplasty in Post–bariatric surgery patients. Plast Reconstr Surg. 2015;135. 10.1097/prs.0000000000001161 [DOI] [PubMed]
- 30.Zeng Y, Lan P. Adjuvant chemotherapy for stage II colon cancer. Zhonghua Wei Chang Wai Ke Za Zhi. 2012;15. 10.1001/jama.294.21.2703 [PubMed]
- 31.Rolnick S, Hensley Alford S, Kucera GP, Fortman K, Ulcickas Yood M, Jankowski M, et al. Racial and age differences in colon examination surveillance following a diagnosis of colorectal cancer. J Natl Cancer Inst Monogr. 2005. 10.1093/jncimonographs/lgi045 [DOI] [PubMed] [Google Scholar]
- 32.Qian F, Eaton MP, Lustik SJ, Hohmann SF, Diachun CB, Pasternak R, et al. Racial disparities in the use of blood transfusion in major surgery. BMC Health Serv Res. 2014;14. 10.1186/1472-6963-14-121 [DOI] [PMC free article] [PubMed]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Supplementary Figures: Supplementary Figure 1: Risk factors associated with blood transfusion after abdominal radical hysterectomy in Midwest or North Central. Supplementary Figure 2: Risk factors associated with blood transfusion after abdominal radical hysterectomy in South. Supplementary Figure 3: Risk factors associated with blood transfusion after abdominal radical hysterectomy in West
Supplementary Tables: Supplementary Table 1: Patient characteristics and outcomes after abdominal radical hysterectomy in Northeast (2010–2019). Supplementary Table 2: Patient characteristics and outcomes after abdominal radical hysterectomy in Midwest or North Central (2010–2019). Supplementary Table 3: Patient characteristics and outcomes after abdominal radical hysterectomy in South (2010–2019). Supplementary Table 4: Patient characteristics and outcomes after abdominal radical hysterectomy in West (2010–2019). Supplementary table 5: Risk factors associated with blood transfusion after abdominal radical hysterectomy in the PSM-matched cohort
Data Availability Statement
The datasets are available at https://www.ahrq.gov/data/hcup/index.html.



