In the present study, over a 7-year period, we identified 47 of 9258 patients (0.51%) who developed PSEH after surgery and among them, 31.91% were the delayed onset hematoma (0.16%). Postoperative SBP and previous spinal surgery at the same level were identified as the independent risk factors for its development. Furthermore, we also found that the early and delayed onset PSEH had different risk factors. To the best of our knowledge, this is the first study that revealed the incidence of delayed onset PSEH in patients undergoing posterior lumbar spinal surgery and risk factors for it.
Incidence
Multiple studies have described delayed onset PSEH in patients with undergoing all level of spinal surgery[8, 11, 13-15]. However, because of its rarity, most studies on it were the case reports and cannot obtain the incidence. Based on our review, only three articles enrolled more than one cases in their studies and two of them estimate the incidence. Uribe J et.al. enrolled 7 patients, first defined the delayed PSEH as an uncommon cause of delayed neurological deterioration, which took more than three days, up to two weeks after the initial surgery and reported the incidence was 0.17%, whereas Anno Masato enrolled 6 patients and reported the incidence was 0.18%[8, 15]. In our practice, in order to avoid the influence of the anatomical characteristics of different region, we limited our study to the cases with posterior lumbar spinal surgery. 15 patients who enrolled in the study were asymptomatic at first 3 days after initial surgery and then developed neurological deterioration in an average duration of 134.6 hours. The prevalence was 0.16% which were close to the previous two studies, indicating that the incidence was similar regardless of the region.
Risk factors
The relationship between blood pressure and hematoma was widely studied in previous studies[4, 5, 16, 17]. According to our study, although univariate analysis revealed that SBP at different time point except for intraoperative were significant higher in delayed onset PSEH group, further multiple logistic regression analysis revealed patients with high postoperative SBP had a 1.10-fold increased risk to develop hematoma. Two possible explanations may account for it as follow: First, patients usually present an elevation in blood pressure after surgery because of wound pain, but the self-regulation mechanisms can rapidly adjust the vessels size to decrease the blood pressure. However, these poorly managed or undiscovered hypertension patients, owing to hardening vessels, self-regulation mechanism failed to regulate the vessel size and the high blood pressure may lead to hemorrhage again after surgery[16, 18]; Second, previous studies have reported the positive relationship between whole blood viscosity (WBV) and hypertension[19-21]. The high postoperative SBP may result in high WBV that could cause blood clots and block the drainage tube. Therefore, it should be noted that not only the preoperative hypertension, but also the postoperative hypertension need to be controlled immediately. It is coincidence with the previous studies. Ohba Tetsuro et. al. found that among the PSEH patients, 4 late-onset patients had obvious postoperative hypertension[18]. And another study from Japanese showed 83.3% of PSEH were in hypertensive state after surgery and development of PSEH can be prevented by controlling the blood pressure.
Another risk factors that is found to be independent associated with delayed onset PSEH is previous spinal surgery at the same level. Many previous studies investigated the role of this factor in PSEH[1, 4, 17]. However, only one study identified it as a risk factor[17]. Moreover, a study on delayed onset PSEH revealed that the rate of previous spinal surgery is much higher than control group[8]. But the samples were too small to conduct the statistical analysis. In our study, based on the information collected, we draw the similar conclusion with these two studies. It is possible because that the second surgery is more difficult and traumatic due to the scar tissues, increasing the risk of bleeding.
Interestingly, in our study, we first found that the risk factors were different for two type of PSEH, indicating that the mechanism of them were different. This may be one reason that why previous studies obtained the controversial results. Proportion of delayed onset PSEH in enrolled samples could influence the statistical analysis.
Clinical features
With regard to initial symptoms, our study was consistent with previous findings that lumbar PSEH often leads to paralysis and pain[1, 15]. In our study, muscle weakness was the most common symptoms regardless of the time of onset, following the dysesthesias and pain. By comparing the two type of PSEH, although JOA Score were similar in two PSEH group prior to surgery, but were significantly worse in delayed onset PSEH group than in early onset group at discharge. Immediate surgical intervention seems to influence it. It is believed that patients with short symptom duration and rapidly surgical intervention are correlated with better outcomes[22, 23]. However, the time from onset to evacuation in delayed onset PSEH is much longer than early one, indicating the spinal surgeons may ignore the possibility of PSEH happened after 3 days and treat it as nerve edema.
This study had some limitations. First, because of the retrospective study, missing data, bias and confounders are inevitable, which may affect the outcomes. Second, due to the rarity of delayed onset PSEH, the sample size was relatively small and cannot conduct a prospective study to verify the risk factors. Future multicenter studies are necessary to solve this problem. Third, because the spinal epidural plexus vein system is a valveless network, a sudden increase in abdominal pressure like a bad cough, sneezing may lead to rupture[24]. Similar cause may affect the results.