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Review

Valproic acid-associated low fibrinogen and delayed intracranial hemorrhage: case report and mini literature review

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Pages 767-770 | Published online: 13 Aug 2013

Abstract

A 41-year-old male had suffered from gradual hearing loss in his right ear for 2 years. Head computed tomography and magnetic resonance imaging scans showed a neoplasm in the cerebellopontine angle region, which was confirmed by the diagnosis of acoustic neurilemmoma by pathological findings after surgery. Following surgery, he routinely received valproic acid (VPA) to prevent seizures. However, the patient presented with hypofibrinogenemia and cerebral hemorrhage after taking VPA for 12 days. The hypofibrinogenemia recurred when VPA was re-administered. After withdrawal of VPA, his fibrinogen concentration rose to normal within several days. As far as we are aware, this is the first case of cerebral hemorrhage due to VPA to have been reported. Herein, as well as reporting on this case, a mini review of the relevant literature is also presented.

Introduction

Valproic acid (VPA) is the main antiepileptic drug broadly administered for all types of seizures. Its excellent efficiency has been shown over four decades of clinical use. Acute toxicity is rare, and when it does occur, it usually follows a benign course.Citation1 Fatal hepatic failure is usually seen following chronic use of VPA.Citation2 The most commonly reported adverse effects are anorexia, nausea, and vomiting. Less frequently, thrombocytopenia; abnormal platelet function; decreased von Willebrand factor concentration; abnormal bleeding time; and activated partial thromboplastin time (APTT) with decreased fibrinogen (Fbg) levels and prolonged prothrombin time (PT) leading to bruising, petechiae, hematoma, and epistaxis have been reported.Citation3 In general, the adverse effects in the hemostatic system are mild or found as abnormal parameters with little clinical significance in laboratory assays.Citation4 Here, we report the case of a male patient with hypofibrinogenemia and cerebral hemorrhage during treatment with oral VPA.

Case presentation

A 41-year-old male had suffered from gradual hearing loss in his right ear for 2 years. Head computed tomography and magnetic resonance imaging scans showed a neoplasm in the cerebellopontine angle region, which was suspected to be acoustic neurilemmoma. Preoperative routine coagulation tests of APTT, PT, thrombin time, Fbg, and platelet count (Plt) were within the normal ranges, and he had no history of bleeding since birth. Clinical examination, biochemistry analysis, and kidney function were normal. The echocardiogram showed normal sinus rhythm. The patient had a history of hepatitis B 20 years before; however, liver enzymes and synthesis function were normal before surgery.

Resection of the neoplasm was successfully performed and blood loss was not excessive during the operation. The results of the pathological examination confirmed the diagnosis of acoustic neurilemmoma. VPA was administered at 20 mg/kg/day to prevent seizures after surgery. Twelve days after surgery, the patient reported headache and examination suggested suspected re-bleeding from the surgical site. This was confirmed in the second surgery. He was treated by decompressive craniotomy to relieve the high pressure.

After the second surgery, a drainage tube was inserted in the incision, since interim bleeding was present (). He received daily transfusions of fresh plasma and cryoprecipitate to improve coagulation function, but the volume of drainage from surgical lesions remained about 30 mL/d. His coagulation function was again tested and he was found to have normal PT, APTT, TT, D-dimer, coagulation factors, and Plt, but a low Fbg level (0.8–1.6 g/L; reference value, 2–4 g/L), high tissue-type plasminogen activator (t-PA) activity (5,400 U/mL; reference value, 300–600 U/mL), and high fibrinogen/fibrin degradation product (FDP) level (60 mg/L; reference value, <10 mg/L). Meanwhile, his biochemistry results, kidney function, and liver function remained normal.

Figure 1 Image after second surgery. Head CT axial image shows the drainage tube placed in the lesion.

Abbreviation: CT, computed tomography.
Figure 1 Image after second surgery. Head CT axial image shows the drainage tube placed in the lesion.

The patient was referred to the Department of Hematology for further management on 30 days following his first surgery. With a supplement of daily Fbg (3 g/d) and use of antifibrinolytic agents for 5 days, the amount of bleeding from the drainage tube decreased gradually and the patient felt his headache relieved without VPA. Coagulation was tested daily and results showed that the Fbg gradually returned to normal within 5 days: from 0.8 g/L on the first day to 1.2 g/L on the second day of treatment, 1.8 g/L on the third day, 2.3 g/L on the fourth day, and 3.5 g/L on the fifth. Coagulation parameters were maintained at normal levels in a week without Fbg transfusion.

Following this, the patient was referred again to the Department of Neurosurgery and VPA treatment was resumed. Amazingly, his Fbg level decreased over time, reaching the minimum level of 0.53 g/L on the fifth day of VPA re-administration. Fortunately, the patient had no bleeding symptoms or manifestation. VPA-associated hypofibrinogenemia was suspected, so the treatment discontinued. Following this, his Fbg level returned to normal and remained stable. The drainage tube was removed 61 days after his first surgery. At follow-up at 6 months, the patient’s hemostatic parameters including Fbg were normal and no symptoms of bleeding were found.

Discussion and mini literature review

The patient presented with hypofibrinogenemia and cerebral bleeding 12 days after taking the recommended dosage of VPA. His bleeding was alleviated as plasma Fbg concentration returned to normal after discontinuing VPA. This suggests a causal relationship between the hypofibrinogenemia, cerebral bleeding, and administration of VPA. Interestingly, this phenomenon recurred on re-administration of the VPA, confirmed by this second use and subsequent discontinuance of the treatment.

VPA was approved by the US Food and Drug Administration in 1978 and is indicated for all seizures including complex partial seizures, simple and complex seizures.Citation5,Citation6 Therefore, it is extensively prescribed as an antiepileptic drug to prevent seizures in patients after neurological surgery. Although VPA-associated coagulopathies are common, significant clinical bleeding complications are rare.Citation4

Fbg, a soluble plasma glycoprotein synthesized by the liver, is converted by thrombin into fibrin during blood coagulation. Congenital deficiency or abnormal function of Fbg was ruled out in this patient, as he had no personal or family history of bleeding, and the results of his preoperative coagulation tests were normal. Therefore, his hypofibrinogenemia during oral VPA administration was acquired. As is well known, acquired deficiency comprises primary and secondary fibrinolysis. However, in this case, the latter (disseminated intravascular coagulation) was easily precluded because the patient had normal Plt count and TT during the course. Thus, the patient’s low Fbg concentration could have resulted from acquired/primary fibrinolysis or synthesis deficiency. The normal liver function during the disease indicated the normal synthesis function of liver. Therefore, the cause of his low Fbg level was probably primary fibrinolysis.

Since the 1970s, several studies have documented a VPA dose-related decrease in Fbg (mean 1.76 g/L; normal, 1.80–4.00 g/L).Citation7,Citation8 In these studies, patients taking other antiepileptic drugs had mean Fbg levels of 2.35–2.72 g/L. One patient taking VPA had their Fbg values decline from 2.10 to 1.25 g/L. After withdrawal of VPA, Fbg rose to 2.90 g/L in 12 days.Citation9 In three VPA-treated patients with low Fbg, fibrin degradation products were normal.Citation8 Koenig et alCitation10 reported that Fbg levels dropped below the lower limit in 12 out of 23 patients who received VPA therapy. Blood coagulation disturbances are common in patients with VPA, but rarely become clinically symptomatic. Ward et alCitation11 reported similar results. In a prospective study, Köse et alCitation12 reported that VPA causes decreased factor VII levels, Plt, factor VIII, Protein C, Fbg, and increased lipoprotein (a) levels. However, no serious bleeding complications were observed in the studies and no correlation was found between Fbg concentration and the dose, blood level, or duration of VPA therapy in the majority of studies ().

Table 1 Literature on valproic acid (VPA)-associated hypofibrinogenemia

The striking elevation of fibrin degradation products in our patient suggested his hypofibrinogenemia was a consequence of excessive consumption rather than deficient production. Although most VPA-associated side effects are mild, we propose that in the case of planned surgery or accidents, routine screening tests comprising Plt, PT, and APTT may not be sufficient. Thus, thromboelastography, von Willebrand factor, and ristocetin cofactor should also be tested to treat the defects properly.

To our knowledge, this is the first case of hypofibrinogenemia and cerebral hemorrhage due to VPA treatment that has been reported. The shorter duration of VPA administration and faster recovery of Fbg level may be why the patient had no bleeding during the second oral VPA administration. The longer time from the brain surgery to the second onset of hypofibrinogenemia may also be partially responsible. The precise mechanisms of VPA-associated low Fbg concentration remain unknown. Recently, Larsson et alCitation13 reported that VPA induces t-PA expression in cultured endothelial cells and this is associated with increased histone acetylation at the t-PA gene promoter. Their results showed that VPA dose-dependently stimulated t-PA mRNA and that protein expression in endothelial cells could reach a two- to fourfold increase at clinically relevant concentrations and tenfold increase at maximal concentrations. This could account for the low level of Fbg in patients who receive VPA treatment.

Disclosure

The authors declare no conflicts of interest in this work.

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