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anesthetic management, general anesthesia, anesthetic considerations, airway difficulties, dwarfism, achondroplasia
Son H. Dang, Ara Samra , Bansi V. Patel, Sebastian Sanchez-Luege
Cite this article as: Dang S H, Samra A, Patel B V, et al. (May 25, 2022) Problematic Airway and Anesthetic Dilemmas for Achondroplastic Dwarfism in the Acute Care Setting: A Case Report. Cureus 14(5): e25336. doi:10.7759/cureus.25336
Patients with achondroplasia often present with anatomical abnormalities and altered cardiopulmonary physiology that significantly increase their perioperative risk for cardiovascular and respiratory complications (e.g., worsening ventilation-perfusion mismatch, imminent desaturation, difficult airway). We describe a 34-year-old achondroplastic male presenting with altered mentation following a traumatic subdural hematoma that necessitated emergent craniotomy evacuation. Initial attempt at intubation was complicated by rapid desaturation and bradyarrhythmia. Subsequently, the patient went into cardiac arrest requiring cardiopulmonary resuscitation. A laryngeal mask airway (LMA) was secured and fiberoptic intubation was achieved in succession. Following return of spontaneous circulation (ROSC), a repeat CT scan showed the subdural hematoma to be stable in size and neurosurgery opted to delay his surgery for conservative management and close monitoring. This case highlights the unique airway challenges and anesthetic considerations in management of achondroplastic patients.
Achondroplasia, also known as Chondrodystrophia fetalis, is the most common type of skeletal dysplasia that affects approximately 1 in 15,000 to 30,000 live births [1]. This genetic disease is caused by a gain-of-function mutation in the fibroblast growth factor receptor 3 gene on chromosome 4 that leads to defective endochondral ossification. Although inherited in an autosomal dominant pattern, about 80% of cases are found to be from new sporadic mutations [2]. Due to their erratic bone formation, these disproportionately dwarfed patients often present with other anatomical defects and altered physiological functions, and are associated with comorbidities (e.g., pectus excavatum, obstructive and restrictive lung diseases) that can severely hinder their anesthetic care. The most common anesthetic obstacles in achondroplasia primarily manifest as difficult airway and spinal features (e.g., maxillary hypoplasia, tracheobronchomalacia, foramen magnum stenosis, kyphoscoliosis, spinal canal stenosis). To avoid detrimental events such as atlantoaxial dislocation, traumatic spinal cord injury, or high spinal anesthesia from occurring, special considerations are warranted when planning the anesthetic method of choice for these patients. Despite meticulous preparation in past, there have been prior reported cases with aborted surgeries, disastrous sequalae, and even death. Our case report intricately discusses the airway challenges and highlight unique anesthetic considerations in an achondroplastic patient undergoing emergency craniotomy evacuation for a traumatically acute subdural hematoma.
A 34-year-old male with achondroplasia was brought in following an assault that resulted in a traumatic head injury. Upon arrival, the primary survey revealed a hemodynamically stable but confused male with a Glasgow coma score of 11, dwarfism features, and right-sided head swelling. The secondary survey was significant for discovering an acute 10 mm thick subdural hematoma located near the right frontal lobe, as seen in Figure 1.
CT of the head demonstrates an acute 10 mm thick subdural hematoma located in the vicinity of the right frontal lobe (shown using blue arrows). There is also a 2 mm midline shift from the septum pellucidum.
Neurosurgical consultation recommended urgent hematoma evacuation. Preoperative history was unobtainable due to the patient's altered mental status. His mother provided limited collateral information that suggested a history of severe obstructive sleep apnea as a child with prior elective tracheostomy at eight years old and reversal at 11 years old. The patient was noted to be a difficult intubation in the past, but his mother could not specify on how the previously intubations were successfully achieved. Review of trauma bay chest x-ray (Figure 2) displayed shallow respiratory volume and vascular crowding without acute pathology.
Chest x-ray reveals poor inspiratory effort versus shallow respiratory volume with only six posterior ribs in the thoracic field. There is vascular crowding with questionable congestion and cardiomegaly.
Intraoperatively, the patient was positioned supine with an assistant providing manual in-line head and neck stabilization. Preoxygenation was achieved via a face mask with 100% inspired oxygen until the end-tidal oxygen concentration was sufficiently greater than 90%. Anesthetic induction was initiated with lidocaine 80 mg, propofol 100 mg, and rocuronium 60 mg. Sugammadex 16 mg/kg and a size 4 intubating laryngeal mask airway (LMA) were kept on hand in the event of an emergency. Rapid sequence intubation was attempted using video-assisted laryngoscopy with a MacIntosh 3 blade. Upon insertion into the oropharynx, the patient was noted to have precipitously desaturated to 60% on continuous pulse oximetry monitoring. The laryngoscope was immediately removed, oropharyngeal secretion was suctioned, and the LMA was inserted with adequate ventilation and oxygenation. At this point, the patient suddenly became bradycardic with a heart rate in the 40s. Intravenous epinephrine 0.5 mg was administered. However, the patient subsequently developed asystole. Advanced cardiac life support (ACLS) protocol was initiated with an additional 0.5 mg intravenous epinephrine given. Ventilation was continued via LMA and return of spontaneous circulation (ROSC) was achieved within one minute. A fiberoptic bronchoscope was introduced through the LMA with subsequent definitive airway establishment via a cuffed 7 mm endotracheal tube.
Neurosurgery decided to delay the surgery given the cardiopulmonary event and a repeat CT head was obtained to re-evaluate the need for urgent craniotomy. Fortunately, on the follow-up CT head, the subdural hematoma remained stable in size and neurosurgery opted for conservative medical management. The patient remained intubated and was transferred to ICU for close monitoring. Ultimately, he had an uncomplicated extubation the following day and was discharged home on hospitalization day six after return of normal neurological function without further surgical intervention.
The anesthetic care for patients with achondroplasia is complex, especially with limited literature on management in the acute setting. These cases are rarely encountered but have the potential for catastrophic outcomes if precautions are not taken in advance. In contrast to elective surgeries, thorough preoperative testing and objective surgical risk stratifications are unlikely available in an emergency. Our case, although not novel, attempts to address the possible problematic features of achondroplasia and highlight the anesthetic considerations in urgent situations where limited information is known.
In comparison to the average human anatomy, these patients are prone to have difficult airway features (e.g., depressed nasal bridge, maxillary hypoplasia, small oral orifice, macroglossia, adenotonsillar hypertrophy, shortened thyromental, tracheobronchomalacia) that could limit the range of motion in their neck, impede sufficient seal for face mask ventilation, and place them at increased risk for upper airway obstruction [3,4]. Structurally, these patients also have a narrower foramen magnum that is funnel-shaped and special care must be taken during intubation positioning and oropharyngeal manipulation [3,4]. Although statistically unreported in adults, one prospective study in achondroplastic infants reported radiological findings for craniovertebral stenosis and craniomedullary compression in 58% and 35% of their study subjects, respectively [5,6]. This emphasizes the accentuated risk for spinal compression and neurological issues with head and neck manipulation. As a result of these fragile cervical anomalies, anesthesia providers should avoid medications that induce myotonic fasciculations and refrain from rapid sequence induction with a depolarizing neuromuscular blocking agent (i.e., succinylcholine). Subsequently, these spasms can preclude ventilatory efforts, worsen neck hyperextension, and exacerbate atlantoaxial instability with the possibility for atlanto-occipital dislocation and cervicomedullary compression.
Patients with achondroplasia also present with thoracic and chest wall abnormalities, including reduced anteroposterior dimensions, rib hypoplasia, scoliosis, and pectus excavatum which can heavily diminish their lung volumes [7]. Other pulmonary comorbidities including central and obstructive sleep apnea, pulmonary hypertension, obesity, obstructive and restrictive lung diseases can synergistically deteriorate their respiratory capacities [4]. Perioperative administration of sedatives, such as benzodiazepines, and opioid analgesics should also be limited unless absolutely required due to their inhibition of spontaneous respiratory drive and further disrupt oxygen exchange. In Table 1, we summarized some the clinical features in achondroplasia and their complementary anesthetic concerns.
This table displays an unexhausted list of clinical features in achondroplasia and their associated comorbidities along with possible anesthetic problems and considerations when managing such patients [8].
As a result of the numerous difficult airway characteristics and rapid desaturation time associated with achondroplasia, a detailed preoperative history can shed light on previous successful approaches, provide key factors to avoid, and influence feasible choices in other anesthetic modalities (e.g., regional anesthesia, intravenous anesthesia). In emergency situations where preoperative history and patient chart review are unavailable, reliance on collateral information, even if limited, can be helpful. Providers should also note that while detailed history or collateral information can assist in management decisions, investigation should not delay an emergency live saving procedure.
Under circumstances where general anesthesia is necessary, awake fiberoptic intubation is indicated in alert and hemodynamically stable patients to secure an airway prior to induction of anesthesia [9]. Of note, an awake fiberoptic intubation was contraindicated in our patient due to his altered mental status and inability to follow commands. Some other contraindications to awake fiberoptic intubations includes patients that are unresponsive, having sustained orofacial traumas, oropharyngeal hemorrhage, basilar skull fractures, laryngeal traumas, allergies to local anesthesia, or concomitant coagulopathies [9]. In cases where awake fiberoptic intubation is contraindicated, an anesthesia contingency plan (e.g., video-assisted laryngoscopy with rescue supraglottic airways, elective surgical airways) can mediate and bypass the probable dilemmas anticipated in achondroplasia. Although uncommon, an ominously feared problem in these patients is the potential for complete airway obstruction occurring post-induction with a resultant cannot-intubate-cannot-ventilate scenario. In these predicaments, it is recommended to use alternative intubation approaches (e.g., alternative laryngoscope blade, intubating supraglottic airway, flexible bronchoscopy) with simultaneous preparation for emergent invasive airways (e.g., surgical cricothyroidotomy, needle cricothyroidotomy with pressure-regulated devices, large-bore cannula cricothyroidotomy, surgical tracheostomy). We also note that some anesthesia providers might not be confident in performing surgical airways in an emergency context with future plans for simulated training in these skills. In one study, 87% of the surveyed anesthesia providers at a tertiary hospital reported that they have not performed an emergent surgical airway before, and most of these providers do not feel confident in performing these procedures in a cannot-intubate-cannot-ventilate scenario [10]. In these instances, standby otolaryngologists or surgeons can assist with surgical airways in rapid succession when alternative intubation approaches have failed. Optionally, elective surgical airways (e.g., retrograde wire-guided intubation, percutaneous tracheostomy, surgical cricothyroidotomy) have gained increasing popularity within recent years. These procedures can be considered on an individualized basis as the initial step when severely complicated airways are anticipated [11]. Our institution follows the American Society of Anesthesiology emergency airway guideline, but this may vary from institution to institution [12]. Table 2 outlines our supplementary tactics in optimizing achondroplastic patients for endotracheal intubation with regard to limiting apneic durations and minimizing hypoxia and subsequent complications.
This table highlights some the preventative measures in anticipating achondroplastic difficult airways. These steps prioritize decreasing the apneic time given the low oxygen reserve in these patients and provide alternative options and advanced measures if an airway cannot be definitively established [13].
LMA: laryngeal mask airway; ET: endotracheal tube
Lastly, we would like to acknowledge other complex drawbacks and limitations in our case. Our patient’s expeditious desaturation with induction of anesthesia can presumably be from atelectasis leading to worsening ventilation-perfusion mismatch, and partly attributable to the significant reduction in residual lung volumes. We could have better optimized this by using prophylactic bronchodilators (e.g., albuterol) prior to induction and placement of high-flow nasal cannula for continuous apneic oxygenation. In conjunction with a sudden onset bradycardia that was unresponsive to epinephrine and further development of pulseless electrical activity, it is hard to exclude possible suspicion for direct cervicomedullary compression [14]. Fortunately, ACLS was promptly initiated with swift achievement of ROSC. Successful ventilation with an intubating LMA was crucial in oxygenating the patient and allowed for definitive endotracheal intubation via fiberoptic bronchoscopy. We chose to perform this alternative intubation method over a surgical airway procedure due to the readily available instruments in our operating room as well as having a less traumatic airway outcome. If this had failed, however, an emergent surgical airway would have been implemented. As exampled by this case, a multitude of complexities can arise when attending to achondroplastic patients in the urgent traumatic setting. Furthermore, limited encounters with these patients hinders active training experience, especially if unfamiliarized physicians stumble upon these cases for the first time. This article aims to shed light on the anesthetic concerns that physicians should integrate into the management of achondroplastic dwarfs.
Achondroplasia, although rare, is likely to be encountered at least once in a medical provider’s career. These patients often present with anatomical and physiological alterations that can impede the safety of different anesthetic modalities, of which a thorough evaluation of the patient and available options should be considered on an individualized basis. If these patients require emergency operations under general anesthesia, difficulty securing an airway is among one of the most prominent issues, especially if the patient is unable to follow commands and preoperative history is unknown or limited. Our case emphasizes awareness in achondroplastic airway dilemmas and perioperative considerations in preventing some of the commonly foreshadowed challenges in their anesthetic management.
Anesthesiology, Jackson South Medical Center - University of Miami Miller School of Medicine, Miami, USA
Anesthesiology, Jackson South Medical Center - University of Miami Miller School of Medicine, Miami, USA
Anesthesiology, Jackson South Medical Center - University of Miami Miller School of Medicine, Miami, USA
Anesthesiology, Jackson South Medical Center - University of Miami Miller School of Medicine, Miami, USA
Human subjects: Consent was obtained or waived by all participants in this study. Jackson South Medical Center issued approval N/A. Our local institutional review board (IRB) at Jackson South Medical Center approved of the case study and waived consent requirement as the patient’s privacy and anonymity were protected. All patient information were thoroughly de-identified throughout the production of the text. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
Dang S H, Samra A, Patel B V, et al. (May 25, 2022) Problematic Airway and Anesthetic Dilemmas for Achondroplastic Dwarfism in the Acute Care Setting: A Case Report. Cureus 14(5): e25336. doi:10.7759/cureus.25336
Peer review began: May 10, 2022 Peer review concluded: May 19, 2022 Published: May 25, 2022
© Copyright 2022 Dang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 4.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
CT of the head demonstrates an acute 10 mm thick subdural hematoma located in the vicinity of the right frontal lobe (shown using blue arrows). There is also a 2 mm midline shift from the septum pellucidum.
Chest x-ray reveals poor inspiratory effort versus shallow respiratory volume with only six posterior ribs in the thoracic field. There is vascular crowding with questionable congestion and cardiomegaly.
This table displays an unexhausted list of clinical features in achondroplasia and their associated comorbidities along with possible anesthetic problems and considerations when managing such patients [8].
This table highlights some the preventative measures in anticipating achondroplastic difficult airways. These steps prioritize decreasing the apneic time given the low oxygen reserve in these patients and provide alternative options and advanced measures if an airway cannot be definitively established [13].
LMA: laryngeal mask airway; ET: endotracheal tube
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