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Perioperative Dexmedetomidine for outpatient cataract surgery: a systematic review



Cataract surgery is one of the most common procedures performed worldwide in the elderly. Various medications can provide effective anesthesia and analgesia for cataract surgery, but undesirable side effects limit the utility of each medication or combination of medications. Dexmedetomidine may serve as an anesthesia adjunct for outpatient cataract surgery in the elderly.


Searches were conducted in Cochrane, Embase, and PubMed for randomized clinical trials investigating the use of dexmedetomidine in adult patients undergoing outpatient, or ambulatory, cataract surgery with sedation and topical or peribulbar block. Ninety-nine publications were identified, of which 15 trials satisfied the inclusion criteria. A total of 914 patients were included in this review. The following data were collected: American Society of Anesthesiologists’ (ASA) physical status and age of study patients; method of blinding and randomization; medication doses and routes of administration; and intraoperative levels of sedation. We also recorded statistically significant differences between dexmedetomidine and other study medications or placebo with respect to the following outcomes: hemodynamic and respiratory parameters; pain; sedation; post-operative nausea and vomiting (PONV); discharge from post-anesthesia care unit (PACU) or recovery times; patient satisfaction; surgeon satisfaction; and effects on intraocular pressure (IOP).


Hypotension with or without bradycardia was reported following bolus doses of dexmedetomidine ranging from 0.5–1.0 mcg/kg with or without a continuous dexmedetomidine infusion. Delayed PACU discharge times were associated with the use of dexmedetomidine, but no clear association was identified between delayed recovery and higher levels of intraoperative sedation. Better analgesia and higher patient satisfaction were commonly reported with dexmedetomidine as well as reductions in IOP.


Overall, this review demonstrates better analgesia, higher patient satisfaction, and reduced IOP with dexmedetomidine for outpatient cataract surgery when compared to traditional sedatives, hypnotics, and opioids. These benefits of dexmedetomidine, however, must be weighed against relative cardiovascular depression and delayed PACU discharge or recovery times. Therefore, the utility of dexmedetomidine for outpatient cataract surgery should be considered on a patient-by-patient basis.

Peer Review reports


Cataract is a leading cause of visual impairment that currently affects almost 25 million Americans and is projected to reach almost 50 million by 2050 [1]. Approximately 2 million cataract operations are performed in the United States each year, and the majority are done in elderly patients [2, 3].

Anesthesia for cataract surgery often includes sedatives and hypnotics (such as propofol, ketamine, or midazolam) with or without opioids, along with topical analgesia or peribulbar block. Propofol and benzodiazepines may induce persistent sedation and respiratory depression, particularly when they are administered in combination with opioids in elderly patients [4]. Opioids may also lead to nausea, vomiting, and perioperative neurocognitive disorders [5].

Ambulatory, or outpatient, cataract surgery demands quick resolution of anesthesia-related effects prior to patient discharge. Postoperative pain, sedation, nausea, vomiting, as well as hemodynamic and respiratory parameters that have not returned to an acceptable percentage of baseline may delay discharge, require additional monitoring, or lead to unexpected hospital admission.

Dexmedetomidine is an alpha-2 agonist with a half-life of approximately 2 h that provides sedation and analgesia without compromising oxygenation and ventilation [6, 7]. However, reported side effects of bradycardia, hypotension, hypertension, and nausea may restrict the use of dexmedetomidine in the ambulatory surgery setting [6,7,8]. Despite the popularity of cataract surgery and the widespread use of dexmedetomidine in anesthesia, no systematic review is currently available that assembles the evidence regarding dexmedetomidine for outpatient cataract surgery.

This systematic review attempts to synthesize the results from randomized clinical trials investigating the use of dexmedetomidine for sedation in adult patients undergoing outpatient cataract surgery. Our review focuses on patient and surgeon satisfaction as well as factors that impact perioperative outcomes: hemodynamic and respiratory parameters; pain; sedation; postoperative nausea and vomiting (PONV); post-anesthesia care unit (PACU) discharge or recovery times; and intraocular pressure (IOP).


Literature search

The authors (JHJ and RA) independently performed initial literature searches in PubMed, Embase, and Cochrane databases for articles published before January 1, 2019, using the following key terms in the English language: “dexmedetomidine” and “cataract surgery.” Additionally, the bibliographies of recovered publications were screened for relevant titles, which were then also reviewed. Eligible studies included randomized clinical trials of adult patients undergoing outpatient, or ambulatory, cataract surgery with sedation supplemented by topical analgesia or peribulbar block.

Data collection

The following data were collected from each randomized clinical trial: age and American Society of Anesthesiologists’ (ASA) physical status of study patients; method of blinding and randomization; medication doses and routes of administration; and intraoperative level of sedation. We also recorded statistically significant differences between dexmedetomidine and other study medications or placebo with respect to the following outcomes: hemodynamic and respiratory parameters; pain; sedation; PONV; discharge from PACU or recovery times; patient satisfaction; surgeon satisfaction; and IOP. The methods by which the studies measured each outcome (such as Visual Analog Score, Numeric Rating Scale, Aldrete’s scoring system, and Ramsay Sedation Scale) were also noted. Data regarding outcomes not expected to impact patient discharge from an ambulatory surgery center (such as incidence of dry mouth) were not recorded.


Ambulatory surgery was defined as surgery after which the patients were discharged from the PACU to home and was considered synonymous with outpatient surgery for the purposes of this review. Unless the authors specifically stated otherwise, it was assumed that all patients were discharged from the PACU to home. Adverse events were only recorded if they were experienced by dexmedetomidine-treated patients. Adverse events of other study medications were not recorded given the heterogeneity of medications analyzed, and the focus of this review was on the effects of dexmedetomidine.

Assessment of study quality

The quality of each study was assessed with 3 measures and given a score between 0 and 5 [9]. One point was awarded if the study was randomized and another point was awarded if the study utilized a double-blind approach. Additional points were given based on the appropriateness of randomization and blinding and if the study included a clear description of withdrawals or dropouts (or specifically stated that there were none). Points were not awarded for inappropriate randomization or blinding.


Study selection

Literature searches in PubMed, Cochrane, and Embase databases identified 99 articles published prior to January 1, 2019. One additional publication was identified after reviewing the bibliographies of recovered studies. After removing duplicates from database searches, 31 publications were screened and 16 were excluded due to the following reasons: ophthalmic procedures other than cataract surgery included in the study (number (n) = 2), primary outcome regarding the effects of dexmedetomidine on regional anesthesia for ophthalmic surgery (n = 2), outcomes not applicable to this review (n = 4), clinical trials without retrievable results (n = 3), study patients received general anesthesia (n = 2), and pediatric patient population (n = 3). All of the remaining 15 eligible studies were included for qualitative synthesis. The method used to identify and screen publications is displayed in Fig. 1: Identification and Screening of Publications. Additional information regarding study designs and demographic information are shown in Table 1.

Fig. 1
figure 1

Identification and Screening of Publications

Table 1 Study Design, Quality Score, and Demographic Data of Included Studies

Quality of studies

Although each study in this review utilized a randomized design, the method of randomization was frequently inappropriate and led to decreased quality scores. Failure to describe withdrawals and dropouts also accounted for low quality scores as noted in Table 1. Most studies utilized a double-blind approach that was considered appropriate.

Routes of administration, dosing, and titration of medications

Two studies titrated dexmedetomidine, remifentanil, and midazolam to pre-determined target levels of sedation as defined by Bispectral index (BIS) scores 70–80 and > 85 [10, 11]. Of the remaining studies, 7 titrated medications to Ramsay Sedation Scale (RSS) scores of 2 or 3 [12,13,14,15,16,17,18]. Two studies administered intramuscular (IM) dexmedetomidine 45 min prior to the regional block [19, 20]. One study employed patient-controlled sedation [21]. Another study utilized target effect site concentrations to titrate remifentanil [22]. Table 2 shows the medication doses, routes of administration, total medication administered, and intraoperative levels of sedation.

Table 2 Route of Administration, Doses, Titration Method, and Total Medication Administered of Included Studies

Intravenous bolus doses of dexmedetomidine were given over 10–20 min and ranged from 0.5–1.0 mcg/kg [10, 12,13,14,15,16, 18, 21,22,23]. Continuous infusions of dexmedetomidine ranged from 0.05–0.7 mcg•kg− 1•hr.− 1 [10,11,12,13,14, 16, 17, 22,23,24]. Variability was also noted in the dosing of midazolam. Bolus doses of intravenous midazolam ranged from 20 to 50 mcg/kg [12, 16, 20]. Two studies titrated continuous infusions of midazolam at 25 mcg•kg− 1•hr.− 1 and 2.5–35.0 mcg•kg− 1•hr.− 1 to BIS > 85 and RSS 2, respectively [11, 16]. There was considerable variety in the total amount of dexmedetomidine and midazolam administered among studies that reported these values as shown in Table 2. Total doses of fentanyl, remifentanil, alfentanil, propofol, and ketamine were not reported in any of the studies. Although medication doses could be estimated from calculations using the average duration of surgery and patient weight, when reported, these calculations were not performed for this review.

Hemodynamic and respiratory parameters

Cardiovascular depression was noted with dexmedetomidine as evidenced by statistically significant decreases in arterial pressure, heart rate, or both. Administration of dexmedetomidine by continuous infusion without initial bolus was not associated with statistically significant decreases in arterial pressure when compared to remifentanil, midazolam, and saline [11, 24]. However, when compared to propofol-alfentanil (combination of propofol and alfentanil), dexmedetomidine infusion titrated to RSS 3 without initial bolus dose led to statistically significant decreases in systolic blood pressure intraoperatively and postoperatively [17]. Additionally, hypotension was reported as an adverse event in 5 patients spanning 2 studies that used continuous infusions of dexmedetomidine at 0.4 mcg•kg− 1•hr.− 1and 0.6 mcg•kg− 1•hr.− 1 without initial boluses; arterial pressures that defined hypotension in these studies, however, were not specifically provided [17, 24]. Omitting a continuous infusion of dexmedetomidine was not associated with preserved arterial pressure or heart rate in any of the studies included in this review [15, 18,19,20]. Table 3 displays the effects of dexmedetomidine on arterial pressure and heart rate compared to other study medications and placebo.

Table 3 Effects of Dexmedetomidine on Arterial Pressure, Heart Rate, and Respiratory Parameters

Heart rate was preserved in 2 studies that did not administer a bolus dose of dexmedetomidine [17, 24]. However, one study comparing the effects of dexmedetomidine to midazolam or saline in 90 patients did not bolus dexmedetomidine, and reported statistically significant decreases in intraoperative and postoperative heart rates [11]. Bradycardia was reported as an adverse event in 5 studies and frequently required atropine treatment [15, 17, 19,20,21].

No statistically significant differences in oxygen saturation (SpO2), end-tidal carbon dioxide (ETCO2) values, or respiratory rates were reported in studies investigating the respiratory effects of dexmedetomidine compared to saline; no sedation; midazolam and fentanyl; propofol and alfentanil; and ketamine and propofol (ketofol) [10,11,12,13,14,15, 17,18,19, 21]. However, there were inconsistent results among studies investigating changes in ETCO2 and SpO2 when comparing dexmedetomidine to midazolam, placebo, and remifentanil [20, 22, 24]. One study demonstrated statistically significant decreases in oxygen saturation with IM dexmedetomidine 1 mcg/kg compared to midazolam 20 mcg/kg and placebo [20]. Better ventilation as evidenced by lower ETCO2 values and increased respiratory rates was noted in dexmedetomidine-treated patients compared to those receiving remifentanil titrated to a target effect site concentration of 1 ng/ml [22]. However, another study comparing dexmedetomidine to remifentanil infusion at 0.05 mcg•kg− 1•min− 1 reported statistically significant decreases in oxygen saturation in dexmedetomidine-treated patients 35–45 min after induction [24].

Analgesia, sedation/cognitive dysfunction, and ponv

There were inconsistent results among studies that investigated pain perception during regional blocks and postoperative analgesia with dexmedetomidine compared to other study medications as shown in Table 4 [11, 13,14,15,16, 18, 20, 21, 24]. One study demonstrated better analgesia as measured by Verbal Pain Scale (VPS) score in patients receiving bolus doses of fentanyl 0.5 mcg/kg and midazolam 20 mcg/kg followed by midazolam infusion at 5–15 mcg•kg− 1•hr.− 1 compared to those receiving dexmedetomidine 0.6 mcg/kg followed by continuous dexmedetomidine infusion at 0.1–0.5 mcg•kg− 1•hr.− 1 titrated to RSS 3 [13].

Table 4 Effects of Dexmedetomidine on Analgesia, Sedation/Cognitive Dysfunction, Nausea/Vomiting, and PACU Discharge/Recovery Time

Better cognitive outcomes as measured by performance on Mini-Mental State Examination (MMSE) were noted in a study comparing dexmedetomidine to remifentanil [10]. Increased intraoperative levels of sedation as measured by Observer Assessment of Alertness/Sedation Scale (OAA/S) and BIS were noted when dexmedetomidine was compared to remifentanil [24]. Increased sedation was also noted with dexmedetomidine compared to saline as measured by BIS and RSS [15, 23]. Increased postoperative sedation lasting up to 3 h postoperatively as measured by 4-point sedation score was reported in one study comparing dexmedetomidine to midazolam and saline [11].

Three studies commented on the incidence of PONV [11, 13, 20]. One study found no statistically significant difference in the subjective assessment of nausea in patients receiving IM dexmedetomidine compared to IM midazolam or placebo, but confidence intervals are unknown [20]. Another study comparing dexmedetomidine to midazolam and saline stated that PONV was not experienced by any patients, while another study reported nausea in 2 patients (2.5%) [11, 13].

Pacu discharge and recovery times

Four studies investigated the time necessary to achieve a pre-determined target Aldrete score [12, 13, 15, 18]. One study noted that dexmedetomidine-treated patients required more time to achieve an Aldrete score of 10 when compared to midazolam-treated patients [median interquartile range (IQR): 45 (36–54) vs 21 (10–32) min, P < 0.01] [12]. Prolonged PACU discharge times were also noted in a study comparing dexmedetomidine to ketofol [mean time to achieve Aldrete score 9 (standard deviation (SD)): 24.9 (4.5) vs 16.1 (2.1) min, P < 0.001] [18]. These findings were not consistent with one study that utilized intravenous dexmedetomidine 1 mcg/kg followed by patient-controlled sedation with dexmedetomidine, which demonstrated no statistically significant differences in Aldrete scores at 30 min postoperatively compared to patients who received no sedation [21]. However, it is not clear from this study if the Aldrete scores achieved in 30 min were acceptable to discharge the patient, such as an Aldrete score 9 or 10 [21].

Intraocular pressure

Seven studies in our review demonstrated significant reductions in IOP [13, 15, 18,19,20,21, 23]. One study reported a 3.8 mmHg decrease in IOP compared to control after a 1 mcg/kg bolus of dexmedetomidine [21]. Intramuscular dexmedetomidine was also shown to reduce IOP, and the greatest reductions were noted in patients who received 1 mcg/kg and 1.5 mcg/kg [mean IOP (SD): 6.8 (3.1) and 6.8 (3.0), respectively] [19]. Another study reported statistically significant decreases in IOP for patients who received dexmedetomidine [mean IOP (SD): 17.10 (1.92) to 13.81 (1.63), P < 0.0001] compared to those who received saline [mean IOP (SD):16.90 (4.11) to 15.41 (3.93), P > 0.05] [15]. Ketofol was also shown to reduce IOP at a rate similar to dexmedetomidine [18].

Preoperative decreases in IOP from dexmedetomidine were not sustained postoperatively. Dogan et al. identified no statistically significant differences in IOP between patients who received dexmedetomidine or the combination of fentanyl and midazolam at 1 h and 24 h following surgery [13]. These findings of non-sustained reductions in IOP are supported by another study comparing the effects of IM dexmedetomidine to IM placebo and IM midazolam, which reported similar mean IOP values in the operated eye in all groups 24 h after surgery [20].

Patient and surgeon satisfaction

Compared to patients who received propofol-alfentanil, patients who received dexmedetomidine reported higher satisfaction scores [Iowa Satisfaction with Anesthesia Scale (ISAS) mean (SD): 50.3 (6.2) vs 42.7 (8.7), P < 0.001] [17]. Other studies corroborate this finding of higher patient satisfaction with dexmedetomidine compared to no sedation, saline, and midazolam [12, 14, 15, 21]. No statistically significant difference in patient satisfaction was noted when dexmedetomidine was compared to ketofol [mean 7-point Likert-like verbal rating scale (SD): 6.3 (0.5) vs 6.1 (0.7), P = 0.084] [18]. Furthermore, no statistically significant difference in patient satisfaction was noted when dexmedetomidine was compared to remifentanil [22].

Surgeon satisfaction was higher in 2 studies comparing dexmedetomidine to saline [14, 15]. There was no statistically significant difference in surgeon satisfaction when comparing dexmedetomidine to the combination of ketamine and propofol, or ketofol, [mean 7-point Likert-like verbal rating scale (SD): 6.4 (0.6) vs 6.2 (0.8), P = 0.067] or midazolam [median 7-point Likert-like verbal rating scale (IQR): 5 (4–6) vs 5 (4–6)] [12, 18]. Lower surgeon satisfaction was noted when dexmedetomidine was compared to remifentanil and midazolam-fentanyl [13, 22]. However, reasons for surgeon dissatisfaction were not specifically stated. Table 5 provides study details regarding patient and surgeon satisfaction.

Table 5 Effects of Dexmedetomidine on Patient and Surgeon Satisfaction


There is noteworthy inconsistency in medication classes, doses, routes of administration, and outcomes analyzed in randomized clinical trials investigating the use of dexmedetomidine for sedation in outpatient cataract surgery. Although strict selection criteria could allow for meta-analysis, the number of relevant studies would be substantially reduced. In attempt to capture relevant outcomes for outpatient cataract surgery, we reviewed the impact of dexmedetomidine on hemodynamic parameters, respiratory parameters, pain, sedation, PONV, PACU discharge times, patient satisfaction, surgeon satisfaction, and IOP.


Hemodynamic and respiratory parameters

Cardiovascular depression secondary to dexmedetomidine is consistent with the known effects of alpha-2 agonists and, particularly, the perioperative administration of dexmedetomidine [6, 7]. Our review demonstrates statistically significant decreases in arterial pressures and heart rates associated with dexmedetomidine in multiple studies utilizing various medication dosages and titration schemes. However, these decreases in arterial pressures and heart rates may not be clinically significant or negatively impact a patient’s perioperative course.

Although there appears to be some association between the bolus administration of dexmedetomidine and decreases in arterial pressures and heart rates, these findings are not supported by all studies. Specific data regarding arterial pressures, heart rates, and associated standard deviations are not retrievable from all publications. Many investigators graphically displayed these data without providing absolute values, thus precluding meta-analyses.

The ability to provide sedation and analgesia while also maintaining oxygenation and spontaneous ventilation is a commonly cited advantage of dexmedetomidine over alternative hypnotics, sedatives, and opioids [6, 7]. Multiple studies in this review demonstrated preserved oxygenation and ventilation [12, 17, 21, 22]. Statistically significant decreases in oxygen saturation in dexmedetomidine-treated patients were noted in two studies [20, 24]. However, the mean oxygen saturation did not fall below 93.14% (± 4.71%) in one study that reported the nadir [24]. Adverse respiratory events, such as the need for emergent intubation, were not reported in any study.

Post-operative cognitive dysfunction and sedation

Dexmedetomidine has been recommended as a safe therapy for reducing the incidence of post-operative delirium in the elderly after non-cardiac surgery in patients admitted to the ICU [25]. POCD and delirium have been associated with inflammatory mediators, which may be suppressed by dexmedetomidine [26, 27]. The incidence of POCD following cataract surgery has been reported at 4.4% and identified risk factors include advanced age and benzodiazepine pre-medication [28]. Overall, the commonest medications resulting in delirium (in the aging brain) include benzodiazepines, morphine, and anti-cholinergics [29]. Mansouri et al. identified no difference in the occurrence of POCD between midazolam and dexmedetomidine following cataract surgery under general anesthesia, although both were superior to placebo [30]. Unfortunately, the studies included in this review primarily focused on intraoperative levels of sedation and cognitive dysfunction, thus limiting our ability to draw conclusions regarding dexmedetomidine and postoperative neurocognitive disorders following cataract surgery.

The studies included in this review attempted to standardize the dosing of medications by targeting specific levels of intraoperative sedation. However, the methods used to assess sedation were variable. One study titrated dexmedetomidine and remifentanil to a BIS of 70–80 and described improved cognitive outcomes with dexmedetomidine as demonstrated by higher performance on MMSE [10]. Another study titrated dexmedetomidine and midazolam to a BIS greater than 85 and described persistent postoperative sedation on a 4-point scale [11]. Inconsistent study methods in assessing sedation preclude meta-analysis of these outcomes.


Nausea is a known side effect of dexmedetomidine [6]. Only one study investigated the subjective assessment of nausea utilizing VAS and found no statistically significant difference between IM midazolam, IM dexmedetomidine, and IM placebo; however, the number of patients who experienced nausea was not provided and the confidence intervals for this result are unknown [20]. After combining the number of patients studied in 2 trials that defined nausea as an adverse event, only 2 patients (1.18%) reported nausea [11, 13].



Pain is one of the most powerful predictors of return to normal activity after surgery [31]. Although pain after cataract surgery is often considered minimal, Porela-Tiihonen reported that 34% of patients had some pain and 9% had more than moderate pain (VAS > 4) in the first few hours after cataract surgery [32].

Better analgesia was noted in patients treated with dexmedetomidine compared to remifentanil, midazolam, saline, and placebo in several studies [11, 14, 21, 24]. These findings are consistent with the known pharmacodynamic properties of dexmedetomidine. However, multiple studies reported no statistically significant difference in analgesia when comparing dexmedetomidine to saline, placebo, midazolam, and ketofol [15, 16, 18, 20]. Peribulbar blocks can provide complete analgesia for cataract surgery, which may limit the ability to identify statistically significant differences in analgesia between dexmedetomidine and other medications or placebo in patients following cataract surgery. Most studies did not investigate analgesia beyond 1 h postoperatively, at which time the peribulbar block may start to dissipate and potentially reveal differences in analgesia between study medications or placebo. Only one study compared dexmedetomidine to the common pairing of midazolam and fentanyl, which exhibited better analgesia [13].

Intraocular pressure

Dexmedetomidine reduces intraocular pressure by its central action [33]. Kim et al. reported that dexmedetomidine attenuated the increases in IOP associated with steep Trendelenburg positioning during laparoscopic radical prostatectomy [34]. Reduced eye pressure may improve surgical operating conditions and decrease the risk for elevated IOP following cataract surgery [35].

Multiple studies in our review demonstrated significant reductions in IOP [13, 15, 18,19,20,21, 23]. However, these decreases in IOP were not sustained postoperatively. These findings may be related to the relatively short half-life of dexmedetomidine, the short duration of surgery during which dexmedetomidine was infused, or both.

Recovery time

Our review demonstrates a tendency for prolonged recovery in patients who received dexmedetomidine, which may limit its utility in the ambulatory surgery setting. When compared to ketofol or midazolam, patients treated with dexmedetomidine required longer times to achieve an Aldrete score of 9 or 10, respectively [12, 18]. In these studies demonstrating prolonged recovery, medications were titrated to RSS 3, which was a common sedation target of other studies included in this review. These findings may be the clinical manifestations of differences in context-sensitive half-times between medications. Overall, PACU discharge and recovery times were infrequently reported by investigators.


Patients who received dexmedetomidine generally reported higher satisfaction scores [12, 14, 15, 17, 21]. Each of the articles included in this review studied patients undergoing monitored anesthesia care, a form of anesthesia in which patient cooperation with the surgeon is critical. Therefore, despite unknown validity and reliability, we considered surgeon satisfaction to be a key component in comparing sedative agents. Surgeons most frequently reported no statistically significant difference in satisfaction associated with the administration of dexmedetomidine compared to other agents [11, 12, 16, 18, 21]. However, lower satisfaction was noted by surgeons when dexmedetomidine was compared to remifentanil [22]. The combination of midazolam and fentanyl was the only study medication group other than saline that was associated with higher patient and surgeon satisfaction scores [13]. Specific reasons for patient or surgeon dissatisfaction were not provided, thus limiting our ability to further analyze these outcomes.


This systematic review is limited by inconsistent study medications, doses, routes of administration, and primary study outcomes of randomized clinical trials. Additionally, the publications included in this review demonstrate variability in the quality of randomization, double-blinding, and reporting of withdrawals and dropouts. These limitations preclude meta-analyses.


Dexmedetomidine offers several advantages over traditional sedatives, hypnotics, and opioids in adult patients undergoing outpatient cataract surgery, such as better analgesia, preserved respiratory function, reduced intra-ocular pressure, and higher patient satisfaction. However, dexmedetomidine is frequently associated with cardiovascular depression, particularly when administered in bolus doses ranging from 0.5–1.0 mcg/kg, and may delay PACU discharge. The advantages and disadvantages of perioperative dexmedetomidine for outpatient cataract surgery should be considered on a patient-by-patient basis.

Availability of data and materials

The datasets supporting the conclusions of this article are included within the article.



American Society of Anesthesiologists’


Bispectral index


Diastolic blood pressure


End-tidal carbon dioxide


Heart rate






Intraocular pressure


Interquartile range


Iowa Satisfaction with Anesthesia Scale

IV :







Mean arterial pressure




micrograms per kilogram

mcg•kg− 1•hr.− 1 :

micrograms per kilogram per hour

mcg•kg− 1•min− 1 :

micrograms per kilogram per minute





mm Hg:

millimeters of mercury


Mini-mental state examination




Numeric rating scale


Observer assessment of alertness/sedation scale


Post-anesthesia care unit


Postoperative cognitive dysfunction


Post-operative nausea and vomiting


Pro re nata


Ramsay sedation scale


Systolic blood pressure


Standard deviation


Standard error

SpO2 :

Oxygen saturation


Visual analog scale


Verbal pain scale


Verbal rating scale


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We would like to thank our colleagues within the Department of Anesthesiology and Pain medicine at the UC Davis Medical Center for their help and support.


No funding was obtained for this study. This study was performed at the UC Davis Medical Center using the equipment and resources available.

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RA helped review the available medical literature on this topic and prepare the manuscript. JHJ helped review the available medical literature on this topic and prepare the manuscript. All authors have read and approved the manuscript, and ensure that this is the case.

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Correspondence to James Harvey Jones.

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Jones, J.H., Aldwinckle, R. Perioperative Dexmedetomidine for outpatient cataract surgery: a systematic review. BMC Anesthesiol 20, 75 (2020).

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