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![]() Open Journal of Anesthesiology, 2011, 1, 1-4 doi:10.4236/ojanes.2011.11001 Published Online October 2011 (http://www.SciRP.org/journal/ojanes) Copyright © 2011 SciRes. OJAnes 1 Perioperative Management of Case of Gynecological Malignancy with Bilateral Deep Venous Thrombosis of Lower Limbs Along with Pulmonary Embolism Mahesh K umar Ar o ra 1, Rakesh Garg2 1Department of Anaesthesiology and Intensive Care, All India Institute of Medical Sciences, New Delhi, India; 2Department of An- aesthesio logy and Int ensive Care, All Ind i a Institute of Medi cal Sciences, New Delh i , India. Email: [email protected] Received S eptember 5th, 2011; revised October 10th, 2011; accepted Oct ober 18th, 20 11. ABSTRACT We describe the anaesthetic management of 45 year female patient with pre-existing deep venous thrombosis (DVT) and pulmonary embolism (PE) who was subsequently scheduled for a laparotomy. Before planning the surgical proce- dures, adequate anticoagulation must be achieved to prevent further complications of DVT, thromboembolism, and pulmonary embolism in particular. The risk of stopping the anticoagulation prior to surgery must be considered and adequately discussed with the patient and surgeons. The anaesthetic plan must be selected keeping in mind the coagula- tion status and the need of anticoagulation in the postoperative period. Keywords: Deep Venous Thrombosis, Pulmonary Embolism, Anaesthesia, Oncology Surgery 1. Introduction Venous thromboembolism (VTE), in the form of deep vein thrombosis (DVT) or pulmonary embolus (PE) is one of the concerns mostly in the postoperative period [1]. The presence of preexisting DVT and PE in patient scheduled for oncologic surgery carries a challenge for anaesthesiologist. As many as 50% of patients who have a proximal DVT develop a PE, and among those who have a clinically significant PE, 70% have evidence of DVT [1]. The underlying etiology for prothrombotic tendency of malignancies is the impact that malignant disease has on the Virchow’s triad of stasis, intimal injury, and hypercoagulability [1]. Patients who have mali gnancy have a si x fold i ncrease d risk o f VTE, and it is estimated that the incidence of VTE in the cancer population is 1 in 200 patients [1-4]. Patients who have brain tumors and adenocarcinoma of the ovaries, pancreas, stomach, colon, lung, prostate, and kidney have a higher risk of VTE than those who have other mali gnanc ie s [4-6 ]. With o ther r isk fac tor s equa l, sur ger y for malignant disease results in a 2- to 3-fold increase in thromboembolism compared with surgery for nonmali- gnant conditions [1,5]. Among the all malignancies, the gynecologic oncology patients have the highest risk of venous thromboembolism [6]. Though postoperative DVT and PE usually remains a concern and various measures are mentioned in literature for its prevention but the presence of DVT and PE preoperatively in a patient scheduled for oncology surgery and its periopera- tive management has not been much described in litera- ture. We present a case of bilateral lower limb DVT with pulmonary embolus scheduled for laparotomy for gynae- cology malignancy. 2. Case History A 45-year-old female weighing 72 kg was scheduled for laparotomy for the excision of abdominoplevic mass and carcinoma ovary. On reviewing the history, patient had fever for last 3 weeks, pain and swelling in both lower limbs since last 10 days. The swelling appeared in the foot and gradually involved the whole of the both lower limbs in 3 - 4 days. Doppler examination of lower limb revealed bilateral deep venous thrombosis (DVT). She was started on inj enoxaparin 0.6 mL once daily since 4 days. Two days back she complained of breathlessness. ![]() Perioperative Management of Case of Gynecological Malignancy with Bilateral Deep Venous Thrombosis of Lower 2 Limbs Along with Pulmonary Embolism She was referred to our institute. On examination, her pulse rate was 92 beats per min, blood pressure of 108/82 mmHg and respiratory rate was 22/min. Investigations revealed haemoglobin 8.4 g/dL. Her D-Dimer by quanti- tative Immunoturbidimetry method was >20 µgFibEq/mL (normal < 0.5). Computed tomographic angiogram revea- led thrombus in left descending pulmonary artery with extension into left lower lobe, infrarenal inferior vena cavae (IVC), bilateral common iliac vein, external iliac vein, common femoral vein, saphenofemoral vein, popli- teal veins along with hepatomegaly and abdominopelvic mass encasing IVC. Haematologists opinion was taken and dose of inj enoxaparin was increased to 80 mg sc twice a day. The risk associated with the surgery and written infor med conse nt was t aken. I VC filt er was p laced in the infrarenal IVC via right transjugular approach. The dose of enoxaparin was omitted on the morning of surgery and patient was premedicated with oral diazepam (10 mg) and pantaprazole (40 mg). Her platelet co unts were 180 × 103/mm3, prothrombin time—13:17 (control:test), aPTT—2 8:30 (c ontrol:test) . In the opera ting roo m, routi ne monitors were attached. Anaesthesia was induced with intravenous fentanyl (150 µg), propofol (140 mg) and lungs ventilated with oxygen in isoflurane (2%). After achieving neuromuscular blockade with atracurium (40 mg), trachea was intubated with endotracheal tube. Left radial artery was cannulated. Ultrasound guided right IJV was cannulated using triple lumen central venous catheter (CVC). Anaesthesia was maintained with isoflu- rane in oxygen and air along with infusions of fentanyl (50 µg/hr) and atracurium (20 mg/hr). Intraoperatively tumor mass was excised and blood loss was 1500 mL, which was replaced with 1500 mL of voluven initially and then with 4 units of packed RBC (after removal of tumor mass) . Pa tient re maine d hae modyna micall y stab le. After completion of surgery, residual neuromuscular blockade was reversed and trachea was extubated. She was shifter to ICU for observation. Inj enoxaparin was restarted 6 hours later. Analgesia was provided with intravenous morphine infusion (1 mg/hr). She remained stable and shifted to ward on 2nd day and discharged home on the 8th day uneventfully. 3. Discussion A number of issues related to pre-existing DVT prior to gynecologic surgery deserve further clarification, the optimal duration of pharmacological treatment, and the optimal duration/modality of prophylaxis to prevent thromboembolism in these high-risk cancer patients. The other concern was bleeding during the perioperative period due to anticoagulation for treatment of DVT and pro-coagulation associated with the malignancy. The pathogenesis of perioperative PE is assumed to be based on a hypercoagulable state that may occur during major surgery and that may extend into the postoperative period [7]. Massive PE is associated with haemodynamic instability and high mortality (30%). So, the treatment options include anticoagulation, thrombolysis, placement of a vena caval filter and pulmonary embolectomy [8]. Further the thrombus extension occurs during the im- mobility in the perioperative period. This chance of thrombus extension and risk of further pulmonary embolus in our patient having bilateral DVT prompted us to insert IVC filter prophylactically. Placement of IVC filter prior to urgent surgery in a patie nt with a DVT has also been described earlier [5,9]. The use of vena caval filters has expanded to include primary venous throm- boembolism (VTE) prophylaxis in special patient popu- lations such as major trauma patients, major surgery patients, advanced malignancy, and neurological or neu- rosurgical patients with paralysis or prolonged immo- bilization. We were apprehensive about the dislodgement of IVC filter intraoperatively as site of its placement was as same as surgical site. Surgeons were careful enough to avoid compression or distortion of the IVC. We started the low molecular weig ht heparin (LMWH) —enoxaparin in our patient as LMWH like enoxaparin, dalteparin, tinzaparin are considered the initial treatment of choice, and may be preferable for patients with cancer [1,5,10,11]. LMWHs are as effective as unfractionated heparin (UFH) for reducing DVT recurrence, thrombus extension and risk of death due to PE. For acute VTE treatment, limitations of UFH include an unpredictable anticoagulant response with the need for frequent monitoring, a relatively narrow therapeutic window, and the potential for severe toxicity, especially heparin- induced thrombocytopenia (HIT) [12]. Importantly, trials of UFH in PE show that many patients are subtherapeutic or supratherapeutic while receiving UFH. In contrast, LMWHs provide a more targeted approach to procoag- ulant complex inhibition, predictable pharmacokinetic and pharmacodynamic characteristics, and no need for anticoagulant monitoring [12]. LMWH is the preferred approach for the initial 5 to 10 days of anticoagulant treatment of the cancer patient with established VTE [2,13]. LMWHs are typically given subcutaneous in a standard weight-based dose (eg, enoxaparin 1.5 mg/kg sc once/day or 1 mg/kg sc twice a day or dalteparin 200 units/kg sc once a day). LMWH is considered to be effective for DVT management in patients with cancer. Thrombolytic therapy of DVT is generally reserved for patients who have limb-threatening thrombosis, symp- toms for less than a week and low risk of bleeding. Abso- lute indications for thrombolytic therapy are a massive Copyright © 2011 SciRes. OJAnes ![]() Perioperative Management of Case of Gynecological Malignancy with Bilateral Deep Venous Thrombosis of Lower 3 Limbs Along with Pulmonary Embolism iliofemoral DVT, especially in the case of phlegmasia cerulea dolens, and a pulmonary embolism that is accom- panied by hemodynamic instability. Our patient had a history of DVT for 3 weeks and was stable hemody- namically, so we avoided thrombolysis when the patient presented to us and started her on enpxaparin. Never- theless, thrombolytics have not been shown to decrease mor t a l i t y in t hese pat ients. The quantitative rapid ELISA, with a sensitivity of 95%, in general has shown the most clinically useful values among the various D-dimer assays [13]. An abnormal D-dimer indicates the need for further testing if PE is suspected. The imaging modalities includes con- trast enhanced multidetector computerized tomography pulmonary angiography (CT angiography) and CT venous phase imaging of the proximal leg veins (CT venography). The gold standard for the diagnosis of PE is Contrast pulmonary arteriography. In the presence of breathlessness, we suspected PE and since D-Dimers were raised, we confirmed the presence of PE with CT angiography. The patients with PE, the gas-exchange abnormalities related to various variables including the size and character of the embolic material, the extent of the occlusion, the underlying cardiopulmonary status and the length of time since embolization [13]. Hypoxemia has been attributed to an increase in alveolar dead space, right-to-left shunting, ventilation/perfusion inequality, and a low mixed venous oxygen level. Classic triad of PE dyspnea, chest pain and hemoptysis is seen in 20% of patients. Our patient had only breathlessness and preope- rative ABG was within normal limits. This may probably be because of thromb osis only in one segment of l ung. So, we conclude, great vigilance is required in the management of a patient with bilateral lower limb deep venous thrombosis with pulmonary embolism. Measures for prevention of further pulmonary embolism should be undertaken prior to urgent oncology surgery. Before planning the surgical procedures, adequate anticoagula- tion must be achieved to prevent further complication of DVT, thromboembolism, and pulmonary embolism. The risk of stopping the anticoagulation prior to surgery must be considered and adequately discussed with the patient and surgeons. The anaesthetic plan must be selected keeping in mind the coagulation status and the need of anticoagulation in the postoperative period. REFERENCES [1] D. A. Anaya and A. B. 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