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Table of Contents
Year : 2011  |  Volume : 27  |  Issue : 3  |  Page : 403-405

Pneumothorax complicating pulmonary embolism after combined spinal epidural anesthesia in a chronic smoker with open femur fracture

1 Department of Anaesthesia and Intensive Care, JLN Medical College and Hospitals, Ajmer, Rajasthan, India
2 Post Graduate Institute of Medical Education and Research, Chandigarh, India

Date of Web Publication11-Aug-2011

Correspondence Address:
Shivendu Bansal
Department of Anaesthesia and Intensive Care, JLN Medical College and Hospitals, Ajmer, Rajasthan
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0970-9185.83695

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Pulmonary embolism during or after regional anaesthesia is although very rare, it has been reported in cases undergoing lower limb orthopedic procedures. We presenting a 48 years old male, a known smoker since 25 years, with history of road traffic accident and open fracture right femur for external fixation. Combined spinal epidural anaesthesia was given. After 35 minutes patient complained dyspnea and chest pain. SpO2 decreased to 82% from 100%. Continuous positive airway pressure with 100% oxygen was given. SpO2 increased from 82% to 96%. Suddenly he had bouts of cough and SpO2 became 79-80% with unstable haemodynamics. On chest auscultation there was decreased breath sounds on right side with limited expansion. Trachea was intubated after inducing anaesthesia with fentanyl 70 μg and thiopental 300 mg. Chest radiograph showed right sided pneumothorax. Intercostal drain with a water seal was put. After 5 minutes HR was 80/min, BP was 110/69 mmHg and SpO2 was 97%. Pulmonary thromboembolism secondary to deep vein thrombosis was suspected and was confirmed by D-dimer Elisa and color Doppler of lower limbs. Patient was shifted to intensive care unit after completion of surgery. Anticoagulant therapy was started. He was weaned from the ventilator on 3rd day and trachea was extubated. Chest drain was removed after 9 days and he was discharged from hospital on 15th post operative day

Keywords: Pneumothorax, Pulmonary Embolism, Smoker

How to cite this article:
Bansal S, Solanki SL, Jain N, Vijayvergia V K. Pneumothorax complicating pulmonary embolism after combined spinal epidural anesthesia in a chronic smoker with open femur fracture. J Anaesthesiol Clin Pharmacol 2011;27:403-5

How to cite this URL:
Bansal S, Solanki SL, Jain N, Vijayvergia V K. Pneumothorax complicating pulmonary embolism after combined spinal epidural anesthesia in a chronic smoker with open femur fracture. J Anaesthesiol Clin Pharmacol [serial online] 2011 [cited 2020 Dec 5];27:403-5. Available from:

   Introduction Top

Pulmonary thromboembolism (PTE) during or after regional anesthesia, although very rare, has been reported in cases undergoing lower limb orthopedic procedures. [1],[2] Patients with fractures of the hip, pelvis, or femur are at high risk of developing deep vein thrombosis and PTE. [3] Chronic smokers are known to be at risk of developing venous thromboembolism [4] and spontaneous pneumothorax. [5] We present a rare case of spontaneous tension pneumothorax complicating PTE in a chronic smoker with traumatic fracture of the shaft of right femur who was administered combined spinal epidural anesthesia.

   Case Report Top

A 48-years-old man weighing 68 kg, and of height 170 cm, was brought to the emergency unit after sustaining an open fracture right femur in a road traffic accident. He was scheduled for external fixation. On examination, the patient was conscious and well oriented. There was no history of loss of consciousness, vomiting or bleeding from oral and nasal cavities. The patient was a smoker since last 25 years (10 cigarettes/day). He denied any other medical comorbidity or surgical treatment in the past. Non-contrast computed tomography (CT) of head was normal, blunt trauma chest and abdomen was ruled out, no cervical spine injury was observed and hemodynamic parameters were also stable. Airway examination revealed mouth opening of 3 cm, thyromental distance of 8 cm, and full range of neck movements. Airway was classified as Mallampatti class II. Preoperative chest radiograph was normal and electrocardiography (ECG) showed normal sinus rhythm. Hemogram, coagulogram and renal and liver function tests were within normal limits. Functional capacity was more than 4 metabolic equivalents (METS).

After explaining the procedure and risk involved to the patient, written informed consent was taken. In the operating room, ECG, noninvasive blood pressure (NIBP), and pulse oximetry were attached and baseline parameters noted. An 18-G intravenous cannula was secured. Preoperative heart rate (HR) was 90/min, blood pressure (BP) 130/80 mm Hg, respiratory rate 16/min, and SpO 2 (on room air) was 97%. Arterial blood gases (ABG) showed pH 7.35, pO 2 98, pCO 2 26, HCO 3 15, BE −5, and SaO 2 97%.

An 18-G epidural catheter was inserted via the L 3 -L 4 space with the patient in a sitting position, using midline approach, and fixed at 11 cm. At the same level, 15 mg of 0.5% bupivacaine heavy was administered in the subarachnoid with a 25-G Quincke's spinal needle. Supplemented oxygen was administered by a venturi facemask (FiO 2 0.5). A sensory loss up to T10 level was achieved with adequate motor paralysis after 9 min and surgery was then started. ECG, NIBP, and SpO 2 were monitored. About 35 minutes after the administration of the subarachnoid block, the patient complained of dyspnea and chest pain. There was a sudden fall in SpO 2 to 82% from 100%. The patient became tachypneic, started coughing and his HR rose to 126/ min. However, BP was within normal limits and ECG showed no marked changes. ABG showed pH 7.36, pO 2 65.6, pCO 2 45, HCO 3 17.2, BE −6.1, and SaO 2 82%. The patient was given continuous positive airway pressure of 100% oxygen with a facemask. SpO 2 increased from 82% to 96%. A sample for D-dimer test was sent with the suspicion of pulmonary embolism. The patient had another bout of cough and SpO 2 fell to 79-80%, BP to 81/54 mm Hg, and HR was 125/min. Dopamine infusion was started. On chest auscultation, there was reduced breath sounds on the right side. ABG values were pH 7.32, pO 2 55.5, pCO 2 54.2, HCO 3 17, BE −6.9, and SaO 2 80%. Anesthesia was induced with intravenous fentanyl 70 μg and thiopental 300 mg. Intravenous vecuronium 7 mg was administered and trachea secured with 8.5 mm endotracheal tube. The position of the tracheal tube was confirmed by capnography. Anesthesia was maintained with isoflurane in 100% oxygen. A chest radiograph was taken immediately, which showed a right-sided pneumothorax. Cardiothoracic consultation was taken and an underwater seal intercostal drain placed. After 5 minutes, HR improved to 80/min, BP 110/69 mm Hg, and SpO 2 97%. The surgery lasted for 130 minutes and was completed without any further complication. Postoperatively, SpO 2 was 97%, BP 105/62 mm Hg, and HR 113/min. The patient was shifted to the intensive care unit (ICU) and mechanically ventilated on Synchronized Intermittent Mandatory Ventilation (SIMV) mode with pressure support.

In ICU, the patient was monitored closely with invasive blood pressure, central venous pressure, oxygen saturation, airway pressure, and serial ABG. The D-dimer test report showed elevated values and color Doppler of lower limbs showed deep vein thrombosis of the right lower limb. Low-molecular-weight heparin therapy (enoxaparin 1 mg/kg subcutaneously 12 hourly) was started. Bed-side two-dimensional echocardiography in the ICU showed mild tricuspid regurgitation, mild pulmonary hypertension [RV systolic pressure (RVSP) = right atrial pressure (RAP) + 31 mm Hg], and hypokinesia of the right ventricular wall.

Postoperative analgesia was achieved with epidural injection of 8 ml of 0.125% bupivacaine 6 hourly, and epidural catheter was removed after 48 hours. The patient was weaned off ventilator support after three days and the trachea was extubated. Oxygen supplementation with venturi facemask (FiO 2 0.5) was given for another two days. Inotropic support was removed on the fourth day and the patient shifted to the ward on the fifth day. Chest drain was removed after 9 days, and he was discharged to home on the 15 th postoperative day.

   Discussion Top

In the case reported, development of severe hypoxia, tachypnea, dyspnea, chest pain, and tachycardia without hypotension following combined spinal epidural anesthesia in a 48-year-old chronic smoker with traumatic fracture shaft of femur raised the suspicion of pulmonary embolism. This was confirmed by raised D-dimer values [6] and color Doppler scan of lower limbs. [7] Systemic arterial hypoxemia is the earliest and most sensitive manifestation of pulmonary embolism and hypotension is less frequent and transient in patients with no prior cardiopulmonary disease. [8] Michael et al.[9] reported a case of intraoperative pulmonary embolism who developed a sudden, marked reduction in arterial oxygen saturation, detected by a pulse oximeter, without hemodynamic change. Diagnosis of acute PTE should be done and based on recommendations of Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED) II investigators. [10] Clinical assessment of low, moderate, and high probability should be done prior to imaging. PIOPED II recommends different imaging modalities according to clinical assessment. In the present case we suspected this as a moderate probability case of acute PTE, and thus D-dimer Elisa test was carried out. Further imaging modalities (CT Angiography) was not done due to unavailability.

In our patient with history of chronic smoking, bouts of severe coughing induced due to the development of acute PTE might have resulted in the development of spontaneous tension pneumothorax. The hypothesis is supported by the sudden worsening after initial improvement in the severity of hypoxemia and dyspnea, along with sudden onset of hemodynamic instability and reduced breath sounds on the right side of the chest. This was further confirmed by chest X-ray.

Chronic smokers are at a higher risk of developing deep vein thrombosis, which can lead to PTE following venodilation due to spinal anesthesia. [11] Chronic smokers are also known be at risk of developing spontaneous pneumothorax following episodes of exertion such as coughing. A definite history of exertion at the onset of pneumothorax in four cases was found in a study by Gupta et al.[12] Smoking may lead to inflammation and obstruction of small airways, accounting for the markedly increased risk of spontaneous pneumothorax. [13] According to Bense et al.,[14] the lifetime risk of developing a pneumothorax in healthy male smokers may be as much as 12% compared with 0.1% in non-smoker males. Rupture of subpleural blebs or bullae is associated with spontaneous pneumothorax. The etiology of such bullous changes in otherwise apparently healthy lungs is unclear. Undoubtedly, smoking plays a role. [14],[15]

Fulminant fat embolism syndrome (FES) should always be considered in the differential diagnosis of respiratory distress in patients with fracture of long bones. Acute onset of FES with worsening hypoxemia has been reported in trauma patients undergoing orthopedic surgeries for long bone fractures.[16] Surgical techniques such as intramedullary nailing and reaming of the long bone have been implicated for massive fat embolism resulting in a sudden onset of pulmonary or cerebral symptoms. [17] Our patient became symptomatic soon after surgery started and was fully conscious until general anesthesia was delivered. He had no cognitive dysfunction following recovery from anesthesia and during the course of illness. There was no petechiae, which are a characteristic feature of FES. [16] Diagnostic criteria such as progressive anemia, thrombocytopenia, and/or leucopenia were absent.

In conclusion, the clinical symptoms like hypoxemia, desaturation, and chest discomfort in patients with traumatic long bone fracture undergoing surgery should be suspected as acute PTE. Further, severe coughing in these patients, especially chronic smokers, can precipitate pneumothorax. Therefore, a cautious vigilance is always necessary even in regional anesthesia to prevent critical events.

   References Top

1.Berry AJ. Pulmonary embolism during spinal anesthesia: Angiographic diagnosis via a flow-directed pulmonary artery catheter. Anesthesiology 1982;57:57-9.  Back to cited text no. 1
2.Newens AF. Pulmonary embolism following spinal anesthesia: Report of a case. Anesthesiology 1971;35:646-7.  Back to cited text no. 2
3.Anderson FA Jr, Spencer FA. Risk factors for venous thromboembolism. Circulation 2003;107(23 Suppl 1):I9-16.  Back to cited text no. 3
4.Holst AG, Jensen G, Prescott E. Risk factors for venous thromboembolism: Results from the Copenhagen City Heart Study. Circulation 2010;121:1896-903.  Back to cited text no. 4
5.Marx J. Rosen's emergency medicine: Concepts and clinical practice. 7 th ed. Philadelphia, PA: Mosby/Elsevier; 2010. p. 393-6.  Back to cited text no. 5
6.Perrier A, Desmarais S, Goehring C, de Moerloose P, Morabia A, Unger PF, et al. D-dimer testing for suspected pulmonary embolism in outpatients. Am J Respir Crit Care Med 1997;156:492-6.  Back to cited text no. 6
7.Kearon C, Ginsberg JS, Douketis J, Crowther MA, Turpie AG, Bates SM, et al. The role of venous ultrasonography in the diagnosis of suspected deep venous thrombosis and pulmonary embolism. Ann Intern Med 1998;129:1044-9.  Back to cited text no. 7
8.McIntyre KM, Sasahara AA. The hemodynamic response to pulmonary embolism in patients without prior cardiopulmonary disease. Am J Cardiol 1971;28:288-94.  Back to cited text no. 8
9.Michael S, Fraser RB, Reilly CS. Intraoperative pulmonary embolism: Detection by pulse oximetry. Anaesthesia 1990;45:225-6.  Back to cited text no. 9
10.Stein PD, Woodard PK, Weg JG, Wakefield TW, Tapson VF, Sostman HD, et al. Diagnostic Pathways In Acute Pulmonary Embolism: Recommendations of PIOPED II Investigators. Radiology 2007;242:15-21.  Back to cited text no. 10
11.Yukioka H, Ryo K, Fujimori M. Severe hypoxia following spinal anesthesia: Possible association with pulmonary embolism. J Anesth 1991;5:303-5.  Back to cited text no. 11
12.Gupta D, Mishra S, Faruqi S, Aggarwal AN. Aetiology and Clinical Profile of Spontaneous Pneumothorax in Adults. Indian J Chest Dis Allied Sci 2006;48:261-4.  Back to cited text no. 12
13.MacDuff A, Arnold A, Harvey J. Management of spontaneous pneumothorax: British Thoracic Society pleural disease guideline 2010. Thorax 2010 ; 65: Ii18-ii31.  Back to cited text no. 13
14.Bense L, Eklund G, Wiman LG. Smoking and the increased risk of contracting pneumothorax. Chest 1987;92:1009-12.  Back to cited text no. 14
15.O'Hara VS. Spontaneous pneumothorax. Milit Med 1978;143:32-5.  Back to cited text no. 15
16.Fabian TC, Hoots AV, Stanford DS, Patterson CR, Mangiante EC. Fat embolism syndrome: Prospective evaluation in 92 fracture patients. Crit Care Med 1990;18:42-6.  Back to cited text no. 16
17.Pell AC, Hughes D, Keating J, Christie J, Busuttil A, Sutherland GR. Fulminant fat embolism syndrome caused by paradoxical embolism through a patent foramen ovale. N Engl J Med 1993;329:926-9.  Back to cited text no. 17

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