To Study Perioperative Changes in Plasma Phenytoin Levels in Patients with Brain Tumor Undergoing Craniotomy and Its Correlation with Postoperative Seizures

Abstract Introduction  Phenytoin, although commonly used for postoperative seizure prophylaxis, exhibits variable results in mitigating seizure frequency following craniotomy. These discrepancies may be linked to a reduction in plasma phenytoin levels subsequent to the surgical intervention. Aims  This prospective study aims to characterize changes in plasma phenytoin levels after craniotomy and their relationship with intraoperative blood loss. Methods  Fifty consecutive patients were enrolled in this study after obtaining written informed consent. These patients had either been on oral phenytoin for at least 7 days or had received an intravenous loading dose before undergoing craniotomy. Serum phenytoin levels were measured 24 hours preoperatively, immediately before craniotomy (prior to skin incision), postcraniotomy (after skin closure), and 24 hours postcraniotomy. Additionally, intraoperative blood loss was calculated using a modified Gross formula. Results  Immediately following craniotomy, there was a statistically significant mean decline of 28.16% in serum phenytoin levels. Furthermore, the analysis revealed a robust positive correlation between the decrease in phenytoin concentration level and several factors, including blood loss during surgery, the duration of the surgical procedure, intravenous fluids administered during surgery, and the occurrence of postoperative seizures. Conclusion  This study underscores the potential utility of routinely measuring perioperative serum phenytoin levels in high-risk patients to prevent postcraniotomy seizures. Moreover, it suggests that patients with substantial intraoperative blood loss may benefit from an additional bolus dose of phenytoin toward the end of the surgical procedure.


Introduction
2][3][4][5] These variations are closely linked to the specific site of the surgical procedure and the nature of the underlying pathology.Of particular concern is the observation that the greatest risk of seizures is within the initial 48 hours following a surgery. 3,44][5] This risk is further exacerbated if the patient has a history of preoperative seizures.Intriguingly, a minority ($5-8%) of patients may even develop entirely new seizures in the postoperative period, referred to as de novo seizures. 6he consequences of postoperative seizures are a matter of serious concern, as they can lead to complications such as increased edema, neurological deficits, prolonged hospitalization, and, tragically, even death. 4,7This increased risk of seizures is primarily attributed to the inflammatory and edematous responses generated during the surgical manipulation and any associated bleeding.Notably, edema typically becomes apparent within 24 to 48 hours after surgery, which also coincides with the period of the highest likelihood of seizure occurrences.
These seizures can have grave repercussions.They disrupt the crucial postoperative assessment of the patient's state of consciousness and can potentially progress to a more severe and life-threatening condition known as status epilepticus. 2,8iven the potential harm posed by postoperative seizures, the use of antiepileptic drugs (AEDs) for prophylaxis has become a common practice in patients undergoing craniotomy.Among these, phenytoin has traditionally been favored by many neurosurgeons, despite the introduction of newer drugs.However, the literature offers varied results regarding the effectiveness of phenytoin in preventing postoperative seizures.
5][16] One hypothesis suggests that the inconsistent results may be attributed to the low plasma phenytoin levels in the immediate postoperative period, but this has not been exhaustively investigated. 3,4,13,17,18n light of these complexities, the primary objective of the study at hand is to closely monitor perioperative changes in phenytoin concentration within the bloodstream of patients undergoing craniotomy.This investigation aims to gauge the associations between these perioperative phenytoin level fluctuations and various surgical variables such as the duration of surgery, the extent of blood loss, and the amount of intravenous (IV) fluid administered.Ultimately, the goal is to assess how these changes in phenytoin levels may influence the occurrence of postoperative seizures.

Materials and Methods
The present observational study was conducted in collaboration between the Department of Anaesthesiology and Critical Care and the Department of Neurosurgery at Pt. B.D. Sharma, PGIMS, Rohtak, Haryana, India.The study included 50 patients of both sexes, aged 18 to 45 years, with American Society of Anesthesiologists (ASA) physical status class I to III.These patients were either on oral phenytoin for at least 7 days or had received an IV loading dose before serum phenytoin monitoring, scheduled for craniotomies for brain space-occupying lesions.Patients/patient attendants who refused to participate in the study, patients who had a history of hypersensitivity to phenytoin, intraoperative massive hemorrhage, preoperative Glasgow coma scale (GCS) less than 14, posterior cranial fossa surgery, patients on AED other than phenytoin, and those requiring intraoperative blood transfusion were excluded from the study.Assessments included clinical history, examinations, GCS, and pupillary responses.A blood sample was taken before induction, immediately postoperation, and after 24 hours of surgery for estimation of haematocrit and serum phenytoin levels.Estimation of phenytoin levels was done using the Chromsystems high-performance liquid chromatography (Chromsystems, Germany) based on the principle of reversed-phase adsorption chromatography. 19ata on surgery duration, IV fluids, urine output, blood loss, and immediate postoperative seizures were recorded.The intraoperative blood loss was calculated from a modification of the Gross formula given below 20 : where ABL is the actual blood loss, BV is the blood volume calculated from the body weight (blood volume ¼ body weight in kg Â 70 ml/kg).Hct(i), Hct(f), and Hct(m) are the initial, final, and mean (of the initial and final) hematocrits, respectively.For statistical analysis, SPSS v15.0 was used, with a p-value less than 0.05 considered significant.

Results
In the study, all the patients older than 18 years were included.The majority fell within the 35-to 45-year age group (68%), ranging from 19 to 70 years.Among the 50 patients studied, 14 were females and 36 were males.The surgical procedures varied, with 24 patients undergoing craniotomy for gliomas, 15 for supratentorial meningiomas, 3 for craniopharyngioma, 3 for epidermoid cysts, 2 for colloid cyst, 2 for trigeminal neurinoma, and 1 for hemangiopericytoma.Serum phenytoin levels were monitored at various points: precraniotomy, Indian Journal of Neurosurgery © 2024.The Author(s).
Perioperative Changes in Plasma Phenytoin Levels in Brain Tumor Craniotomy Kumawat et al.
postcraniotomy, and 24 hours postoperatively.The mean preoperative level was 15.0481 AE 1.795 µg/mL, which decreased to 10.810 AE 1.722 µg/mL postcraniotomy and then rose to 14.140 AE 1.635 µg/mL 24 hours postoperatively (►Table 1).The mean change in phenytoin level during surgery was 4.238 AE 1.107 µg/mL, constituting a 28.16% decrease from the preoperative levels.Before surgery, all 50 patients had serum phenytoin levels within the therapeutic range, but immediately after surgery, only 33 out of 50 patients (66%) maintained the therapeutic levels.The remaining 17 patients had serum phenytoin levels below the therapeutic range, that is, less than 10 µg/mL.Postoperative seizures were observed in six patients, with five of them having postoperative phenytoin levels below 10 µg/mL and one within the therapeutic range (10-20 µg/mL).The details of the site of lesion, histopathology, and type of seizure are described in ►Table 2. Each patient was administered an additional IV dosage of phenytoin, and for three of them, a second-line AED was also introduced into their treatment regimen.Postseizure, a computed tomography (CT) scan of the head revealed bleeding at the operative site in two patients, while another exhibited cerebral edema.The patient with an epidermoid cyst displayed symptoms of aseptic meningitis, which was subsequently managed with IV steroids.Preoperative hematocrit levels averaged 35.59 AE 2.22%, which decreased to 32.70 AE 2.26% postoperatively, with a significant p-value of 0.0001.The operative details showed that the mean duration of surgery was 4.480 hours, with mean blood loss of 369.47 AE 85.71 mL and mean IV fluid infusion of 2,379.00AE 442.86 mL.Statistical analysis revealed a strong positive correlation between the decrease in phenytoin levels and blood loss, duration of surgery, IV fluids administered, and postoperative seizures (►Table 3).A comparison between the seizure and nonseizure groups showed that the decrease in phenytoin levels, blood loss, and mean phenytoin levels was statistically significant, while the duration of surgery and IV fluids were not (►Table 4).Additionally, there was a statistically significant difference in the mean fall in serum phenytoin levels in the postoperative period between patients who had seizures (5.18 AE 1.61 µg/mL) and those who did not (4.11AE 0.99 µg/mL), with a p-value of 0.03.

Discussion
Postoperative seizure is a significant complication that can occur following neurosurgical procedures.These seizures are associated with various negative outcomes, including aspiration pneumonitis, increased mechanical ventilation, prolonged intensive care unit (ICU)/hospital stay, increased edema, and even death.Perioperative Changes in Plasma Phenytoin Levels in Brain Tumor Craniotomy Kumawat et al.
hydrocephalus, venous edema, or infarction.Factors such as the generation of free radicals due to blood product leakage or disruptions in ion balance caused by ischemia/hypoxia can trigger these seizures.The influx of calcium during ischemic or hypoxic conditions plays a crucial role in the release of excitatory neurotransmitters and the formation of free radicals, further increasing the risk of postoperative seizures. 24,25Seizures can also be a manifestation of systemic complications such as electrolyte imbalance, infection, or abnormal glucose levels.The standard of care for seizure treatment and secondary prevention is the use of AEDs. 9,26However, the use of perioperative AEDs solely for prophylaxis has been a topic of controversy.A recent meta-analysis has shown that perioperative AED prophylaxis for brain tumor surgery significantly reduces the risk of early postoperative seizures. 8e current cross-sectional study aims to observe changes in phenytoin concentration in the blood of brain tumor patients undergoing craniotomy and assess the association between these perioperative phenytoin level changes, duration of surgery, amount of blood loss, and amount of IV fluid administered.The findings of this prospective study revealed a mean decrease of 28.16% in phenytoin levels following craniotomy, which could potentially be a contributing factor to postoperative seizures.Previous studies have also investigated the changes in perioperative phenytoin levels, and upon comparison, all studies, except for the study conducted by Phunsawat et al, 27 demonstrated a statistically significant decrease in mean phenytoin levels during the immediate postoperative period 3,4,27,28 (►Table 5).The decrease in phenytoin levels was found to be positively correlated with the amount of blood loss, operative time, and IV fluid administration in all studies, including the present one.This could be attributed to the loss of phenytoin-rich blood during surgery, which is then replaced by phenytoin-deficient fluids.Hemodilution, resulting in decreased plasma protein concentration, may have also contributed to this phenomenon, as phenytoin is highly protein bound.Furthermore, longer durations of surgery typically involve greater blood loss, increased phenytoin deficit fluid/blood transfusion, increased excretion, and subsequently lower phenytoin levels.It is important to note that a sudden drop in perioperative phenytoin levels could potentially increase the risk of postoperative seizures, similar to the abrupt withdrawal of an anticonvulsant drug in a nonsurgical setting. 3,4,27,28aintaining a therapeutic level of phenytoin is crucial for effective seizure control, as patients with subtherapeutic levels are more susceptible to seizures. 4,13The occurrence of postoperative seizures is a complex phenomenon, and subtherapeutic level of phenytoin is one of the contributing Table 4 Comparison of all parameters used in study between two groups, one having seizures and other not having any seizures in their post-operative period      Based on this study, it is suggested that a loading dose of 7 to 15 mg/kg may be administered after the closure of dura to prevent a sudden drop in phenytoin levels in the immediate postoperative period, as recommended by other researchers as well. 18,29Previous studies, along with the present one, have observed that postoperative seizures can occur even when phenytoin levels are within the therapeutic range.Therefore, when a patient experiences an episode of seizure, appropriate investigations should be conducted in addition to measuring serum phenytoin levels.Intraoperative precautions, such as minimizing retraction, meticulous dissection, gentle handling of neural tissue, avoiding excessive coagulation, frequent irrigation, and maintaining proper hemostasis, are of paramount importance in reducing the incidence of seizures.

Conclusion
The occurrence of seizures after surgery varies among patients, and several factors contribute to the development of seizures during the postoperative period.One significant factor is maintaining an adequate level of phenytoin in the bloodstream.This research emphasizes the importance of regularly monitoring plasma phenytoin levels in high-risk patients undergoing craniotomy, as inadequate phenytoin levels significantly increase the risk of postoperative seizures.To mitigate this risk, it is crucial to uphold appropriate perioperative phenytoin levels, and in cases involving substantial blood loss, administering an additional half loading dose of phenytoin (7-10 mg/kg) during surgery is highly advisable.By understanding and managing these factors, neurosurgeons can work to reduce the incidence of postoperative seizures and improve patient outcomes.

Indian
Journal of Neurosurgery © 2024.The Author(s).

Table 1
Phenytoin levels and hematocrit, blood loss during surgery, duration of surgery, and intravenous (IV) fluids given during surgery and their standard deviation Indian Journal of Neurosurgery © 2024.The Author(s).

Table 3
Showing correlation and significance of changes in phenytoin concentration in blood during surgery with blood loss during surgery, duration of surgery, intravenous (IV) fluid given during surgery and postoperative seizures

Table 5
Comparison of different studies showing mean perioperative phenytoin (PHT) level, mean blood loss, and mean duration of surgery Abbreviation: NC, not calculated.

Table 6
Different studies showing number of patients with seizure having therapeutic and subtherapeutic level of phenytoin (PHT) Studies Perioperative Changes in Plasma Phenytoin Levels in Brain Tumor Craniotomy Kumawat et al.