Postoperative complications with neuromuscular blocking drugs and/or reversal agents in obstructive sleep apnea patients: a systematic review

A literature search was performed according to the Preferred Reporting Items for Systematic Reviews guidelines [23]. The search strategy was carried out with the help of a research librarian familiar with literature searches for systematic reviews. We screened published articles describing postoperative complications in surgical patients with OSA and/or obesity who were given NMBD and/ or reversal agents intraoperatively. We included articles that described residual NMB. The literature databases searched were MEDLINE (1946 to April 4, 2017), ePub ahead of print, MEDLINE in-process, and other non-indexed citations (up to April 4, 2017), Embase (1947 to April 4, 2017), Cochrane Central Register of Controlled Trials (up to February, 2017), Cochrane Database of Systematic Reviews (2005 to April 4, 2017), PubMed (1946 to April 4, 2017), Web of Science (1900 to April 4, 2016), Scopus (1960 to April 4, 2017), ClinicalTrials.Gov (up to April 6, 2017), WHO ICTRP (up to April 6, 2017).

The search terms included the Medical Subject Heading keywords “obstructive sleep apnea,” “obesity” and “neuromuscular blockade”. The following text keywords were used for the literature search: “obstructive sleep apnea syndrome,” “sleep disordered breathing,” “obesity hypoventilation syndrome,” “apnea or apnoea,” “hypopnea or hypoapnea,” “muscle relaxant,” “rocuronium,” “atracurium,” “cis-atracurium,” “vecuronium,” “mivacurium,” “suxamethonium or succinylcholine,” “rapacuronium,” “pancuronium,” “skeletal muscle relaxant,” “neuromuscular reversal agents,” “neostigmine,” “edrophonium,” “sugammadex,” “residual neuromuscular block,” “neuromuscular blockade reversal,” “postoperative residual neuromuscular blockade,” “post-extubation complications”, “perioperative complications,” and “postoperative complications.”

Inclusion criteria were: (1) adult surgical patients (≥18 years old) with OSA confirmed by polysomnography (PSG), history, or suspected by screening questionnaire; (2) patients in the study were given NMBD and/ or NMBD reversal agents intraoperatively; (3) reports on postoperative adverse events, particularly respiratory events were available (4) published studies were in English and (5) randomized controlled trials (RCTs) or observational cohort studies. Exclusion criteria were: 1) case reports and review articles; 2) studies with no information on OSA status; and 3) studies with no information on postoperative pulmonary complications (PPCs) and/or residual NMB.

Studies were selected independently by 2 reviewers (RH and AT) who screened the titles and abstracts to determine whether the studies met the eligibility criteria. Disagreements in screening and data extraction were resolved by consulting another author (MS or JW). A citation search by manual review of references from primary or review articles was also performed.

The following information was collected from each study: author, year of publication, type of study, sample size of OSA and non-OSA group, OSA status (diagnosed or suspected), apnea hypopnea index (AHI), PSG data, and sleep questionnaire data, type of surgery, age, gender, body mass index, NMBD used and dose, NMBD reversal agent used and dose, neuromuscular monitoring, postoperative complications, incidence and type of complication.

PPCs included were airway obstruction, hypoxemia and desaturation, decreased inspiratory capacity, respiratory muscle weakness, residual NMB, increased secretions, bronchospasm, atelectasis, pleural effusion, pulmonary edema, respiratory failure, apnea, respiratory failure, re-intubation, postoperative mechanical ventilation and intensive care unit (ICU) admission. We contacted the authors of the studies for missing data. Only one responded [24].

The risk of bias was evaluated using the Cochrane risk of bias tool [24] for RCTs. For observational cohort studies, the Newcastle-Ottawa tool [25] was used to rate risk of bias and study quality by assessing the selection, comparability and outcome of each study. For evaluation of the quality of evidence, we utilized the Oxford Center for Evidence Based Medicine Levels of Evidence [26].

Our initial electronic search identified 4123 articles, of which four studies were included in the qualitative synthesis (Fig. 1). Forty-five articles were further obtained through citation search and one was included. Three studies describing PPCs in OSA and non-OSA patients were excluded because the number of OSA patients with PPCs was not clearly shown [27‐29]. Finally, five studies with at total of 1126 patients were included in this systematic review [30‐34].

Among the 5 included studies, 2 were RCTs [32, 33] with 426 patients and 3 were observational studies [30, 31, 34] with 700 patients. These were single-center studies from various countries including the United States, Brazil, Turkey and Spain. The types of surgery included were intra-abdominal, bariatric, musculoskeletal, head and neck and otolaryngology surgeries. Descriptive data of the study population are summarized in Table 1. Altogether, 587 diagnosed or suspected OSA patients and 539 non-OSA patients were included. Three studies reported postoperative complications in OSA vs. non-OSA patients who received NMBD [30‐32] and 2 reported postoperative complications in OSA patients administered sugammadex vs. neostigmine [33, 34]. One study [30] used the Berlin questionnaire along with preoperative polysomnography to diagnose OSA, and in another study [31], the authors used STOP-BANG criteria for OSA risk assessment. In the other three studies, patients were already diagnosed with OSA. All the included studies used the TOF watch for intraoperative NMB monitoring. In PACU, only Pereira et al. used the TOF Watch for residual NMB monitoring. Unal et al. performed clinical assessment of muscle strength in PACU.

The definitions of postoperative pulmonary complications varied between the different studies (Table 2). Some studies did not define the PPCs or included minor symptoms that are not consistent with previous studies reporting PPCs. Only one study described cardiac complications [33]. The details of postoperative adverse events from each study are shown in Table 3.

The risk of bias in both RCTs was moderate overall (Table 4). The risk of bias was fair in the observational studies by Ahmed et al. [30] and Llaurado et al. [34] and that of Pereira et al. [31] was good (Table 5). The quality of all studies was moderate to low (Table 1).

Are patients with OSA who received NMBD as part of general anesthesia at higher risk for postoperative complications than patients without OSA?

We identified one RCT [32] and 2 observational studies [30, 31] with 378 diagnosed or suspected OSA patients and 345 non-OSA patients. Since the studies were heterogeneous and differed in study design, types of surgery, and outcomes reported, a meta-analysis was not performed.

In a RCT of 352 patients, Sudre et al. found that OSA vs. non-OSA patients were at higher risk of developing respiratory failure (OR 6.88, 95% CI 2.36–20.05, P = 0.0004) [32]. In an observational study of 40 patients, Ahmed et al. reported that OSA was not an independent risk for postoperative hypoxemia in the first 24 h after laparoscopic bariatric surgery (P = 0.97) [30]. In another observational study of 340 patients, Pereira et al. [31] showed that patients with high risk of OSA (STOP-Bang score ≥ 3) vs. low risk patients (STOP-Bang 0–2) more frequently experienced residual NMB (24% vs. 17%, P = 0.035), and mild/moderate hypoxia (9% vs. 3%, P = 0.012). There was no significant difference in other respiratory complications between OSA vs. non-OSA patients who received NMBD [30‐32]. Based on the included studies, OSA vs. non-OSA patients who have received NMBD may be at higher risk of hypoxemia, residual NMB and respiratory failure (Oxford LOE between 2 and 3) (Table 1).

Does the choice of NMBD reversal agent affect the risk of postoperative complications in OSA patients?

We identified one RCT [33] and one observational study [34] with a total of 206 OSA patients that evaluated the impact of reversal agents on postoperative complications (Table 2). Two reversal agents, sugammadex and neostigmine, were compared.

In the RCT of 74 OSA patients, Unal et al. found that sugammadex decreases the incidence of PPCs {desaturation, hypoxemia, apnea, airway manipulation, airway usage, re-intubation, CPAP (continuous positive airway pressure), invasive mechanical ventilation (Table 3)}. Eight patients (21.6%) had significant bradycardia (P = 0.028) with six requiring treatment with atropine [33]. In an observational study of 145 OSA patients undergoing laparoscopic bariatric surgeries, sugammadex was found to decrease the incidence of postoperative chest radiograph changes {atelectasis, pleural effusions (P = 0.007)} compared with a historical cohort receiving neostigmine. No difference in clinical outcomes including postoperative mechanical ventilation or hospital stay was found [34]. Oxford LOE for both studies was between low to moderate (Table 1).

There is growing concern that residual NMB is associated with adverse respiratory outcomes in patients undergoing anesthesia [22, 35‐38]. Residual NMB is particularly important to avoid in OSA patients since OSA is associated with an increased risk of postoperative respiratory and cardiac events, ICU transfers, and longer hospital stay [6‐8, 39, 40]. Anatomical risk factors increase vulnerability to airway collapse during sedation or sleep in OSA patients. The retropalatal, retroglossal and hypopharyngeal regions of the upper airway in OSA patients are the most common sites of collapse during sleep or sedation, causing obstruction [41]. This collapse can occur because of variations in transmural pressure, such as decreased intraluminal pressure or increased external tissue pressure, or a reduction in the longitudinal tension on the pharynx [42]. Magnetic resonance imaging (MRI) studies show that the airway in OSA patients is different from the normal airway because of thicker lateral pharyngeal walls with an anteroposterior elliptical configuration, unlike the horizontal configuration in the normal airway leading to airway narrowing [42].

Upper airway dilators are more vulnerable to the effects of NMBD compared to the respiratory pump muscles [6, 15]. Even at levels producing mild blockade, as measured by train of four ratio (TOFR) 0.7–.9, NMBD increased upper airway collapsibility and impaired compensatory genioglossus response to negative pharyngeal pressure challenges [43]. Due to the pathophysiology of the disease, patients with OSA may have increased vulnerability to the effects of NMBD and reversal agents [42, 43]. In a large retrospective database study of 530,089 patients with 32,789 diagnosed OSA patients, Memtsoudis et al. [8] found a 5-fold increase in intubation and mechanical ventilation in OSA patients after orthopedic surgery and a 2-fold increase after general surgery compared with non-OSA patients. They concluded that OSA is an independent risk factor for developing pulmonary complications [8].

In our review, two observational studies found contrary results for hypoxemia [30, 31]. Ahmed et al. found that OSA patients were not at higher risk of developing hypoxemia than non-OSA patients. A significant limitation is the small sample size (n = 41; OSA = 31, non-OSA =9). Also, the use of supplemental oxygen at 3 l per min via nasal cannula for 24 h postoperatively in all patients may have masked the occurrence of desaturation episodes. The incidence of hypoxemia was significantly higher in morbidly obese patients with or without OSA, suggesting the importance of morbid obesity as an independent risk factor for PPCs [30]. Pereira et al. concluded that mild/moderate hypoxia was the only PPC in the immediate postoperative period that occurred more frequently in patients with suspected OSA [31]. Schumann et al. studied the relation between metabolic syndrome and surgical factors (duration and type of surgery) with PPCs in bariatric patients [44]. They found that increasing age, BMI, ASA status, metabolic syndrome, OSA, asthma, congestive heart failure, surgical factors were independently associated with PPCs. PPCs and metabolic syndrome were significantly associated with increased postoperative mortality [42]. Many other studies have also reported that OSA patients are at a higher risk for hypoxemia than non-OSA patients [5, 35‐38].

Residual NMB was monitored in all the included studies by TOFR using acceleromyography before reversal agent, and on admission in the PACU [30‐32]. In the general population, residual NMB increases the incidence and risk of PPCs in a dose dependent manner [16]. To avoid PPCs, neuromuscular monitoring is important to reduce residual NMB; this is even more important in OSA patients as it has been reported as an associated risk factor for early PPCs requiring invasive airway placement or intensive respiratory care [7, 35]. Ideally, before extubation, any residual NMB should be ruled out by quantitative neuromuscular monitoring in a train of four (TOF) supramaximal peripheral nerve stimulations administered over two seconds [45]. A consensus statement on the perioperative use of neuromuscular monitoring was recently published by a panel of clinician scientists with expertise in NMB monitoring [46].^. They recommended that whenever a NMBD is administered, neuromuscular function must be monitored by observing the evoked muscular response to peripheral nerve stimulation [46]. The American Society of Anesthesiologists recommends that: 1) patients at increased perioperative risk from OSA should be extubated while awake; 2) full reversal of NMB should be verified before extubation; and 3) when possible, extubation and recovery should be carried out in the lateral, semi-upright, or other non-supine positions [47].

Several studies have examined sugammadex vs. neostigmine in patients without OSA. Brueckmann et al. and Sabo et al. found that the use of sugammadex vs. neostigmine for NMBD reversal reduced residual NMB in PACU [48, 49]. In a systematic review of 17 RCTs of non-OSA patients, Abad-Gurumeta et al. found a significant reduction in residual NMB with sugammadex vs. neostigmine but no difference in the rate of adverse respiratory events that required tracheal re-intubation [50]. We found some, albeit limited evidence to support a reduction in PPCs in OSA patients receiving sugammadex vs. neostigmine. In a 2017 Cochrane review, significantly less bradycardia occurred in patients who received sugammadex vs. neostigmine [36]. In the OSA patients, Unal et al. also reported less bradycardia in the sugammadex vs. neostigmine group [33].

In the morbidly obese patients, Gaszynski et al. found that sugammadex reversed rocuronium more quickly than neostigmine with a mean time to 90% of TOF (2.7 vs. 9.6 min, P < 0.05), and a higher TOF at the PACU (109.8% vs 85.5%, P < 0.05) [51]. In the obese vs. patients with a normal body mass index, the duration of action of NMBD may be prolonged which may lead to increased incidence of residual NMB in PACU [52]. In both studies, PPCs and the number of OSA patients were not described [51, 52]. In contrast, in a review of 27 studies with over 1400 patients receiving sugammadex, Monk et al. reported that there were no clinically significant differences in recovery times to a TOFR of 0.9 between patients with and without obesity, following reversal of NMBD with sugammadex [53].

The Society of Anesthesia and Sleep Medicine recommended that OSA patients should be identified and optimized preoperatively and the diagnosed OSA patients who are already on home CPAP device should continue with CPAP perioperatively [54]. These precautions should be taken when NMBD are administered for OSA patients.

There were few studies evaluating the effect of NMBD on postoperative complications in OSA vs. non-OSA patients, and the effect of different reversal agents on postoperative complications in patients with OSA. The sample size of included studies was small. There was a lack of consistent definitions for PPCs among the different studies, and some studies reported symptoms such as cough or breath-holding which are not accepted definitions of PPCs [55]. Most studies used rocuronium in standard intubation and maintenance doses, however, benzylisoquinolines were used by Llaurado et al. (cisatracurium) and Sudre et al. (atracurium) only in the control group to compare with rocuronium. In addition, the effect of opioids and residual anesthetics on postoperative pulmonary complications was not evaluated in the studies. OSA patients with co-existing morbidities such as chronic obstructive pulmonary disease, renal or liver disease were not evaluated. As OSA is associated with significant comorbidities, such as morbid obesity, obesity hypoventilation syndrome, pulmonary hypertension and cardiovascular diseases, it is unclear what the contribution of OSA or its comorbidities are towards PPCs [52]. Only Pereira et al. measured TOF in the PACU. Finally, one study used the STOP-Bang questionnaire to identify high risk OSA and the diagnosis was not confirmed by polysomnography [31].