Bone Cement Implantation Syndrome (BCIS)

Bone Cement Implantation Syndrome (BCIS)

Bone Cement constituents:

-Bone cement is an acrylic polymer that is formed by mixing two sterile components: 

a) Powder:

1-Polymer: Polymethyl methacrylate/co-polymer (PMMA) 

2-Initiator: Benzoyl peroxide (BPO) 

b) Liquid:

1-Monomer: Methyl methacrylate (MMA) 

2-Accelerator: N, N-Dimethyl para-toluidine (DMPT)/diMethyl para-toluidine (DMpt) 

-To make the cement radiopaque, a contrast agent is added, either zirconium dioxide (ZrO₂) or barium sulphate (BaSO₄). 

-When the two components are mixed, the liquid monomer polymerizes around the pre-polymerized powder particles to form hardened PMMA. During this polymerization process, heat is generated, due to an exothermic reaction, and reaches temperatures of around 82–86 °C. 

Incidence:

-The incidence of BCIS in cemented orthopedic procedures is approximately 20%. 

-The incidence of a severe reaction resulting in cardiovascular collapse within this group is 0.5-1.7%. 

Orthopedic procedures incidence:

-Cemented hemiarthroplasty (highest incidence) 

-Total hip replacement 

-Knee replacement surgery 

BCIS typically occurs during:

-Bone cementation and prosthesis insertion 

-Femoral reaming (before cementation) 

-Joint reduction and limb tourniquet deflation (after cementation) 

Patients at high risk of cardio-respiratory compromise:

-Male sex 

-Increasing age 

-ASA class III / IV 

-Significant cardiopulmonary disease 

-Chronic obstructive pulmonary disease 

-Use of diuretics 

-Use of warfarin 

Conditions that can increase the incidence of BCIS:

-Osteoporosis, Bone metastasis, and Concomitant hip fractures. 

These conditions may be associated with increased or abnormal vascular channels, through which marrow contents can more readily migrate into the circulation, resulting in emboli. 

Pathophysiology of BCIS:

a) Embolization of the Medullary Contents:

-During surgical cementation and prosthesis insertion, the cement is intentionally pressurized to force it into the interstices of the bone, to improve bonding between the cement and bone. 

-The cement then expands in the space between the bone and the prosthesis, further pressurizing air and the medullary contents, forcing them into the circulation. These embolic contents include fat, marrow, cement, air, bone particles, and aggregates of platelets and fibrin. 

-When these medullary contents embolize, they may reach the lungs, heart, and/or coronary circulation, causing the characteristic hypoxia and right ventricular dysfunction, leading to hypotension. 

b) Histamine release, Hypersensitivity, and Complement activation:

-Contact with bone cement (Methyl Methacrylate), leads to an increase in blood levels of anaphylactoid complements (C3a and C5a) and histamine, which are potent mediators of vasoconstriction and bronchoconstriction. 

-These mediators result in an increase in pulmonary vascular resistance, causing ventilation/perfusion disturbances, hypoxia, right ventricular failure, and cardiogenic shock. 

Clinical Picture:

-Hypoxia 

-Sudden loss of arterial blood pressure 

-Pulmonary hypertension 

-Arrhythmias 

-Loss of consciousness 

-Cardiac arrest 

-Under general anesthesia, a significant drop in systolic blood pressure (SBP) may herald cardiovascular collapse, whilst a sudden drop in end-tidal pCO₂ may indicate right heart failure leading to a catastrophic reduction in cardiac output. 

-In an awake patient under a regional anesthetic, early signs of BCIS may include dyspnea and/or altered sensorium. 

BCIS Severity Spectrum:

a) Non-fulminant BCIS:

-Characterized by a significant, yet transient, reduction in arterial oxygen saturation and SBP in the peri-cementation period. 

b) Fulminant BCIS:

-With profound intraoperative cardiovascular changes, progressing to; arrhythmias, shock, or cardiac arrest. 

Classification of BCIS Severity: based on the degree of hypoxia, hypotension, and conscious level (Table 1)

Table 1: Classification of BCIS Severity

Prophylaxis:

a) Anesthesia:

1-Ensure adequate hemodynamic optimization pre- and intra-operatively 

2-Keep SBP within 20% of the pre-induction value 

3-Prepare vasopressors in case of cardiovascular collapse 

4-Confirm awareness that cement is about to be prepared/applied 

5-Maintain vigilance for cardiorespiratory compromise 

b) Orthopedic:

1-Inform the anesthetist before cement application 

2-Wash and dry the femoral canal 

3-Apply cement retrograde, utilizing a suction catheter and intramedullary plug in the femoral shaft 

4-Avoid excessive pressurization (3rd generation technique) 

Management:

-Administration of 100% inspired oxygen is first-line therapy, with airway control if necessary. 

-Invasive hemodynamic monitoring (if not already in place), should be established. 

-In cases of severe BCIS (when the patient has been arrested, or in a peri-arrest condition), standard advanced cardiopulmonary life support (ACLS) algorithms and procedures should be followed. 

-Fluid resuscitation to maintain Rt. Ventricle preload, and inotropes to support ventricular contractility.

-Vasopressors (such as Phenylephrine and Noradrenaline) primarily causes peripheral vasoconstriction, and increase aortic blood pressure, which in turn supports coronary artery blood flow, and thus improves myocardial perfusion and contractility. 

-Use of vasopressors and inotropes should be continued into the postoperative period as necessary, under the management of the intensive care unit (ICU).

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Treacher Collins Syndrome

Treacher Collins Syndrome:

-A craniofacial defect associated with developmental anomalies of the first arch. 

-Abnormalities vary from minimal, to complete syndrome. 

-The syndrome is named after Edward Treacher Collins, an English surgeon and ophthalmologist, who described its essential traits in 1900. 

-Patients may require anesthesia for maneuvers to improve upper airway obstruction temporarily, or for correction of some of the congenital defects. 

-Airway obstruction and a requirement for multiple operations increase the need for tracheostomy. 

Etiology:

-It is due to mutations in TCOF1, POLR1C, or POLR1D genes. TCOF1 gene mutations are the most common cause of the disorder, accounting for 81 to 93% of all cases. POLR1C and POLR1D gene mutations cause an additional 2% of cases. In individuals without an identified mutation in one of these genes, the genetic cause of the condition is unknown. 

Preoperative Abnormalities:

1. Features may include mandibular and malar hypoplasia, antimongoloid palpebral fissure, macrostomia, irregular maloccluded teeth, microphthalmia, lower lid defects, cleft palate, high arched palate, macroglossia, and auricular deformities. 

2. Associated abnormalities include mental retardation, deafness, dwarfism, cardiac defects, choanal atresia, and skeletal deformities. 

3. Chronic upper respiratory tract obstruction and obstructive sleep apnea, which can lead to growth retardation and/or cor-pulmonale. 

Anesthetic Problems:

1. Upper airway obstruction: in neonates, this may require urgent temporary maneuvers, such as stitching the tongue to the lower lip 

2. Excess secretions: may impede induction of anesthesia 

3. Inhalational induction: may be difficult 

4. Difficult tracheal intubation 

5. Obstructive sleep apnea may occur postoperatively 

6. Pulmonary edema 

Intraoperative Management:

Recommendations:

1-Monitoring by pulse oximetry, to detect airway obstruction, is crucial. 

2-Avoid respiratory depressant drugs, both for premedication and postoperatively 

3-Use drying agents 

4-Never give muscle relaxant until the airway has been secured. 

Airway Management:

-Several methods have been proposed to overcome the problem of difficult intubation, some in the awake patient and some under general anesthesia: 

a) In Awake Patients: 

1-Awake intubation or awake direct laryngoscopy to visualize the vocal cords. 

2-Direct laryngoscopy, with the patient in the sitting position, and using a 5-G feeding tube taped to the side of the laryngoscope to give oxygen. 

3-The Augustine guide (Figure 1): can be used for nasotracheal intubation in an awake, sedated patient.

Figure 1: Augustine guide

4-Fibreoptic bronchoscope or Tracheostomy under local anesthesia: 

In small infants, the ‘tube over bronchoscope’ technique is not always possible because of the small size of the tube, therefore a Seldinger type approach may be necessary: 

-After the administration of atropine, ketamine IM, and topical lidocaine, a fibreoptic bronchoscope (OD 3.6mm, L 60 cm, and suction channel 1.2 mm) was passed through one nostril. 

-The tongue was held forward with Magill forceps, until the vocal cords were seen, but not entered, because of the risk of total obstruction. 

-Under direct vision, a Teflon-coated guidewire with a flexible tip was passed via the suction channel into the trachea. 

-The bronchoscope was carefully removed leaving the wire in place, and an ID 3mm nasotracheal tube was then passed over it into the trachea. 

Pediatric bronchoscopes of 2.5 mm diameter are now available, but their very fineness makes them less easy to handle than the 4-mm bronchoscopes). 

b) In Anesthetized Patients: 

1-Jackson anterior commissure laryngoscope (Figure 2): 

-The head is elevated above the shoulders, with flexion of the lower cervical vertebrae and extension at the atlanto-occipital joint. The laryngoscope is introduced into the right side of the mouth. Only the tip is directed towards the midline, the proximal end remaining laterally so that a further 30 degrees of anterior angulation can be obtained. 

-The narrow, closed blade prevents the tongue from falling in and obscuring the view of the larynx. When visualized, the epiglottis is elevated, and the larynx entered. Intubation is then achieved by passing a lubricated tube, without its adaptor, down the laryngoscope. It is held in place with alligator forceps whilst the laryngoscope is withdrawn.

Figure 2: Jackson anterior commissure laryngoscope

2-The Bullard intubating laryngoscope (Figure 3):

-It can be used to achieve nasotracheal intubation.

Figure 3: Bullard intubating laryngoscope

3-Tactile nasal intubation: 

-Inhalational induction with sevoflurane, and the tongue is pulled downwards and forwards. The tube is initially used as a nasal airway, whilst the index and middle finger are used to palpate the epiglottis, through which the tube is then passed. 

4-Laryngeal mask airway: 

-Inserted under propofol anesthesia and can be used as a conduit for the passage of a fibreoptic bronchoscope.

5-The use of an assistant to pull out the tongue with Magill forceps, and at the same time to apply cricoid pressure, to assist laryngoscopy. 

Postoperative Management:

-The tracheal tube should remain in place until the patient is fully awake. 

-Patients should be nursed in a high dependency area postoperatively. The combination of sleep apnea and drugs with CNS-depressant effects may make them particularly susceptible to respiratory arrest.

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