Abstract
Hypotensive anesthesia is a commonly used technique that aims to reduce intraoperative blood loss, consequently improving surgical field visibility and the need for blood transfusions post-operatively. It is widely used in major maxillofacial surgeries with a high risk of intraoperative bleeding. The aim is to reduce the patient’s systolic blood pressure to 80 to 90 mm Hg and mean arterial pressure (MAP) by at least 30% of preoperative blood pressure or keeping a minimum MAP of 50–65 mmHg. Hypotensive anesthesia not only provides a bloodless surgical field but also helps to identify various anatomical structures. There are various pharmacological and non-pharmacological methods to induce hypotensive anesthesia. The decision to induce hypotensive anesthesia should be based according to the general condition of the patient, the extent of the surgery, and in coordination with the operating surgeon. The target blood pressure should be adjusted according to the patient’s preoperative status and coexisting illness. The risk of organ hypoperfusion should be kept in mind. Close intraoperative monitoring with optimal patient selection is important for good patient outcomes.
Keywords: Controlled hypotension, hypotensive agents, hypotensive drugs
INTRODUCTION
One of the key components of balanced anesthesia is maintaining the perfusion of vital organs during surgery. Blood pressure is an important vital sign that determines organ perfusion and cardiac output. Hence, normotensive anesthesia is the routine standard practice. However, in some scenarios, hypotension is induced deliberately. This technique is known as hypotensive or controlled anesthesia.[1]
Initially proposed by Gardner in the 20th century, the concept of hypotensive anesthesia has revolutionized anesthesia practice.[2] Hypotensive anesthesia is a commonly used technique that aims to reduce intraoperative blood loss, consequently improving surgical field visibility and the need for blood transfusions post-operatively.
This technique is used in many fields, like middle ear surgeries, oro-maxillary surgeries, spinal surgeries, orthopedic surgery, neuro surgeries, cardiovascular, and liver transplant surgery. It not only provides a bloodless surgical field but also helps to identify various anatomical structures.[3] The aim is to reduce the patient’s systolic blood pressure to 80 to 90 mm Hg and mean arterial pressure (MAP) by at least 30% of preoperative blood pressure or keeping a minimum MAP of 50–65 mmHg.[4] This article mainly focuses on hypotensive anesthesia in maxillofacial surgeries with major intraoperative bleeding.
Effect of hypotension on various organs
Lungs
Pulmonary Alveolar macrophages – These are phagocytes, which are located in the alveolar compartment of the lungs, protecting against inhaled pathogens and debris. They modulate inflammation by producing anti-inflammatory cytokines like interleukin-10 and promote blood flow in the lungs. They also release vasoactive mediators, nitric oxide, and prostaglandins which help to regulate blood flow and vascular tone in the lungs.
Pulmonary alveolar macrophage (PAM) reduces with the anti-Trendelenburg position or sitting position and increases dead alveolar space with the risk of hypoxia and hypercapnia.[5]
Pulmonary blood flow gravitates to the dependent areas, particularly in the head up position. Thus, non-dependent lungs are ventilated but not perfused adequately, hence increasing dead space. Further use of vasodilators to induce hypotension abolishes the hypoxic pulmonary vasoconstriction response, thus increasing intra-pulmonary shunt. All these factors combined, result in hypercarbia, an increase in arterial-end tidal carbon dioxide (etCO2) gradient and hypoxaemia. Therefore, it is important to have regular measurements of partial pressure of carbon dioxide (PaCO2) during controlled hypotension.[6]
For the same reason, the arterial oxygen tension (PaO2) may also be reduced during hypotension. Thus, a higher fraction of inspired oxygen (FiO2) may be necessary to maintain the oxygen saturation within normal limits, during hypotensive anesthesia.
CNS
Cerebral blood flow normally remains constant over a MAP range of 60 to 150 mm Hg. In patients with chronic hypertension, the autoregulation curve is shift to the right. While in patients with controlled blood pressure on antihypertensive treatment, the curve tends to shift back toward normal. It is recommended to keep the patient in normocapnia status [CO2 partial pressure (PaCO2) between 35–40 mmHg][7]
Renal
As per the recent studies, there is a strong relation between intraoperative hypotension and postoperative acute kidney injury (AKI). Moreover, autoregulation of renal blood flow is impaired during general anesthesia, and renal blood flow is compromised with even moderate decreases in arterial blood pressure. Hence, it is recommended to maintain MAP >65 mmhg.[8]
CVS
Increase myocardial oxygen demand due to any reason requires simultaneous increase in the coronary artery blood flow. This may be hampered by hypotensive anesthesia which may reduce coronary blood flow due to the decrease in afterload or/and preload.
Hence, hypotensive anesthesia is associated with significant intraoperative risk of myocardial infarction.[6]
Pros of hypotensive anesthesia
The main goal of hypotensive anesthesia is to decrease the MAP either by reducing the cardiac output or by reducing the systemic vascular resistance or both. However, inducing hypotension purely by decreasing cardiac output is not an ideal method, because the maintenance of adequate blood flow to organ is essential. Systemic vascular resistance can be decreased by peripheral vasodilatation of the resistance blood vessels.[9]
The maxillofacial region is highly delicate and vascular, which requires quite precise and accurate surgery. There is a risk of a generous amount of blood loss, which demands the instant availability of various blood products.[6] This is not only a concern in terms of availability issues but also the risk of transmission of infectious diseases and other complications associated with blood transfusion.[10] Besides this, uncontrolled bleeding in head and neck surgeries can lead to hematoma formation which can further compromise the airway.
Therefore, induced hypotension becomes important in such a scenario. It decreases the overall duration of surgery thus leading to improved quality of the surgical field[11] while avoiding major complications. The integrity of vital structures is maintained, and tissue regeneration and healing are also quick.
Cons of hypotensive anesthesia
Not every patient planned for surgery can tolerate hypotensive anesthesia; therefore, careful patient selection is a must. The risk of hypotension-associated hypoperfusion of vital organs like the brain, heart, and kidney is well known. Patients with ischemic heart disease, fixed cardiac output state, and vascular disease are more susceptible to this.[12] Moreover, patients with known hypertension have less tolerance for low blood pressure due to their higher set autoregulation point. In addition, they have contracted blood volume which can further exaggerate hypotension. Hence, modification of the hypotensive technique by keeping a higher safety margin along with adequate volume replacement should be performed in these patients.[1]
If the decrease in cerebral blood flow is more than the decrease in the cerebral metabolic requirement for oxygen, cerebral ischemia may develop. In normotensive adult patients, cerebral ischemia can arise at a MAP threshold of 40–50 mmHg in the orthostatic position and 45–55 mmHg in the supine position.[13]
Cerebral ischemia may be detected by the clinical availability of several non-invasive near-infrared spectroscopy (NIRS)-based cerebral oximetry devices that can give early warning of reduced oxygen delivery. Blasi et al.[14] conducted a study and found that remifentanil-based general anesthesia with propofol or sevoflurane changed the muscle microcirculation in different ways. These changes were measured by non-invasive quantitative NIRS effectively, which is a technique that considers the optical tissue properties of an individual.
Zhang conducted a randomized control trial in FESS patients and found that a 30% decrease from the baseline MAP leads to a decrease in the intraoperative blood loss, improved quality of the surgical field, and the shortening of the duration of surgery in the hypotensive group. However, the fall in regional cerebral oxygen saturation (monitored by NIRS) from the baseline was only ~ 5%, which was within safe levels, and no cerebral desaturation events were noted in the intervention group.[15]
Tang et al.[16] conducted a study in patients (<60 years age) undergoing noncardiac surgery to note the association of intraoperative hypotension with postoperative AKI and observed that there was a significant risk of postoperative AKI when intraoperative MAP was less than 55 mm Hg for more than 20 min.
Similarly, Walsh et al.[17] found a graded relationship between more than 5 min spent with a MAP of less than 55 mm Hg or a MAP of 55 mm Hg to 59 mm Hg and stage I AKI and myocardial injury.
In an observational study of 5,127 patients, Sun et al.[18] found that postoperative AKIN stage I AKI was associated with an intraoperative MAP of less than 55 mm Hg for more than 10 min and a MAP of less than 60 mm Hg for 11 min to 20 min.
A retrospective cohort analysis was performed by Salmasi et al.[19] to assess relationship between various absolute and relative characterizations of intraoperative hypotension and myocardial injury after noncardiac surgery (MINS) as well as AKI. They found that even a MAP of 65 mm Hg which is a clinically acceptable pressures correlated with both MINS and AKI. At lower pressures, the association was stronger, and even a low pressure for a short time was associated with poor outcomes.
The goal is to keep the target blood pressure moderately low to allow a reduction in bleeding without disturbing the microcirculatory autoregulation of the vital organs, i.e. heart, brain, or kidney.[20]
Contraindications of hypotensive anesthesia
Controlled hypotension is not safe to practice in certain conditions. Those can either be related to patient, drug, or anesthesia limitations.
Absolute contraindications
include cerebrovascular disease with severe carotid stenosis,[21]
symptomatic or severe aortic or mitral stenosis
stage IV chronic kidney disease
known drug allergy
lack of experience or knowledge in the subject
Relative
Cerebrovascular disease
Uncontrolled Diabetes mellitus
Severe hypertension
Coronary artery disease
Anemia, hemoglobinopathies, polycythaemia
Hepatic disease
Renal disease
Severe lung disease
Pregnancy
Inadequate monitoring
Hypovolemia
Monitoring and perioperative preparation
Hypotensive anesthesia demands meticulous monitoring of the patient. This includes arterial oxygen saturation, electrocardiography, end tidal carbon dioxide monitoring, temperature, urine output, and non-invasive or invasive measurement of blood pressure (depending on the procedure and patient’s comorbidities).
Before the induction of hypotension, a period of cardiovascular stability must be ensured by giving titrated dose of anesthetic drugs for induction and maintenance. Since non-invasive blood pressure is intermittent, episodes of hypotension may be missed. Hence, invasive blood pressure monitoring is necessary especially if a rapid-onset hypotensive agent is used. Radial artery pressure is usually preferred since it accurately measures central arterial pressure and is easy to cannulate.[22]
To ensure adequate perfusion of vital organs during hypotensive anesthesia, cardiac output (CO) monitoring can also be done if available. Few methods for CO monitoring are described below:
Lithium dilution cardiac output (LiDCO): Where lithium chloride is injected and CO is calculated by measuring the concentration change over time.
Flowtrac – It is a minimally invasive method to measure CO. It utilizes a proprietary algorithm to analyze the pulse pressure waveform obtained from an arterial catheter and provide real-time CO monitoring.[23]
The patient should be positioned carefully. The nasotracheal tube should be fixed gently with minimum pressure on the nares to avoid skin necrosis. Similarly, air cushion should be placed in pressure areas like sacrum to prevent pressure sores.
Pharmacological methods
There are various strategies for achieving hypotensive anesthesia. Newer techniques rely on the natural hypotensive effect of the anesthetic drugs. The ideal drug should be short-acting, dose-dependent, with minimal effect on vital organs, and quick excretion without any residual toxic metabolites.[24] This comprises mainly drugs which are either used alone or as an adjunct to limit dose requirement and side effects of other drugs.[25]
Inhalational anesthetic agents include isoflurane, sevoflurane, and desflurane which are used commonly. They are primarily vasodilators, thus decreasing systemic vascular resistance. However, volatile anesthetics when used alone in high doses for controlled hypotension can cause hepatic or renal injury and delayed recovery from anesthesia.[26]
Recent studies have combined inhalation agents with drugs like nitro-glycerine, adenosine, morphine, labetalol, and esmolol to reduce the concentration and side effects of each drug. A study conducted by Rossi et al.[27] shows that desflurane reduces blood loss in comparison with sevoflurane and contributes to a better surgical field. Overall, the use of inhalation anesthetic agents solely as hypotensive agent is controversial, and an adjuvant is required to induce truly controlled hypotension.
Propofol
It is one of the most commonly used intravenous anesthetic agent which acts by enhancing the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) through GABA type A (GABAA) receptors. Hypotension is a well-known side effect associated with the use of propofol which is often desirable in surgeries requiring deliberate hypotension. It has rapid onset and recovery, hence, mostly used as a part of total intravenous anesthesia (TIVA). Complete and smooth recovery without any residual effects makes it a good choice for day-care surgery.[28,29]
Opioids – Popularly used in anesthesia for their analgesic effects, few opioids can induce hypotension which may not be desirable routinely. However, they have been used successfully as adjuvant to other hypotensive agents where controlled hypotension is indicated. Out of the commonly available opioids like morphine, fentanyl, alfentanil, sufentanil, and remifentanil, the latter has gained popularity due to its rapid onset and long elimination half-life.[30]
Remifentanil is an ultra-short-acting mu receptor agonist. It has context sensitive half-life of about 5 min. It is used mostly as an adjuvant with propofol in TIVA. Degoute et al.[24] conducted a study using remifentanil and propofol in TIVA and found that they provided good surgical conditions and desired hypotension for tympanoplasty.
Vasodilators – like nitro-glycerine (NTG) and sodium nitroprusside rapidly control BP because of their short onset and duration of action. They produce nitric oxide which causes vascular smooth muscle relaxation. Among these, sodium nitroprusside for a long time has been a drug of choice for hypotensive anesthesia. However, side effects like tachyphylaxis and cyanide toxicity impose challenges in the administration of these drugs. Nitro-glycerine in comparison with sodium nitroprusside has a slightly slower action, but it does not cause myocardial ischemia, rebound hypertension, or any toxic metabolites.[31]
Betablocker – They have been used efficiently for reducing blood pressure during surgery either alone or in combination with other agents. Based on their duration of action and selectivity, many β-blockers are in clinical use.
Labetalol blocks both α and β receptors. α-receptors blockage leads to vasodilatation, of blood vessels, thus causing hypotension, while β-receptor blockage prevents reflex increase in heart rate. Studies have demonstrated better hemodynamic, decrease bleeding, and improved surgical visibility with the use of labetalol as compared to other agents. It is generally given in a dose of 0.25 mg/kg followed by continuous infusion of 0.5–2 mg/min which can be titrated up to 10 mg/min. It has a long elimination half-life of 5.5 hours which may cause delayed postoperative hypotension that maybe a cause of concern.[32]
Esmolol is a short-acting cardio-selective drug with antagonist action on the β-1 receptor. It has negative chronotropic and inotropic action, thus reducing CO, and heart rate, eventually decreasing blood pressure. It can be given intravenously as a bolus or infusion and the blood pressure returns to normal once the infusion is stopped. Dose is 1000 mcg/kg bolus over 30 seconds, followed by 150 mcg/kg per min infusion, with a maximum dose of 300 mcg/kg per min. Its ability to prevent reflex tachycardia and rebound hypertension makes it a good choice among β-blockers for hypotensive anesthesia. However, β-blockers need to be avoided in patients with a history of asthma due to the risk of bronchospasm associated with them.[33]
Dexmedetomidine, an adrenergic receptor (α-2-AR) agonist, offers a promising role in hypotensive anesthesia. This is due to its wide spectrum of properties which includes sedation, analgesia, anxiolysis, and sympatholytic action at both central and peripheral levels. It preserves cardiovascular and respiratory functions and lacks any major side effects. Besides this, it is easy to administer and quite predictable with other anesthetic agents.[34] Various studies have proven that dexmedetomidine decreases surgical bleeding while maintaining hemodynamic stability, thus providing desirable surgical field.[35,36]
This makes it a near-ideal agent for hypotensive anesthesia. However, it may cause bradycardia which may limit its use in certain circumstances. Postoperative sedation and dry mouth are a few side effects associated with the use of dexmedetomidine. It can be given in a loading dose 1 mcg/kg/I.V infusion over 10 min followed by a maintenance dose of 0–0.2 0.7 mcg/kg/hour.[37] Sajan et al.[38] compared dexmedetomidine and labetalol for induced hypotension in ear nose and throat surgeries and found better hemodynamic with dexmedetomidine and faster recovery with labetalol.
Clonidine is another α-2 adrenoceptor agonist which is commonly used in clinical practice to treat hypertension, migraine and menopausal flushing. It is less selective to α-2 receptor as compared to dexmedetomidine (220:1 vs. 1620:1), hence a less potent hypotensive agent.
Goswami et al.[39] compared the efficacy of dexmedetomidine and clonidine infusion to produce hypotensive anesthesia in patients undergoing orthognathic surgery and surprisingly found no significant difference between the two groups. However, dexmedetomidine provided better surgical field and surgeon satisfaction and reduced the need of rescue analgesia which was an additional advantage.
Magnesium sulfate
It has been well-recognized as a versatile drug for a long time. Its mechanism of action includes antagonism of the non-competitive N-methyl-D-aspartate receptors, decrease catecholamine release, and anti-nociceptor action, thus decreasing response to noxious stimuli. It is a vasodilator and decreases systemic vascular resistance, thus producing hypotensive effects. Besides this, it has also anti-arrhythmic action. Hence, it can be used as an adjuvant for controlled hypotension. Elsharnouby et al.[40] conducted a study to study the hypotensive effect of magnesium sulfate in FESS patients where it was given in a dose 40 mg kg−1 i.v. as a bolus preinduction and 15 mg kg−1 h−1 by continuous i.v. infusion intraoperatively.
Lidocaine is a commonly used amide local anesthetic agent. It is also used to treat ventricular arrythmia and blunt the hypertensive response of laryngoscopy. Its negative inotropic action on the heart along with the sympatholytic effect may contribute to hypotension.
Karami et al.[41] recently conducted a study to compare labetalol and lidocaine for the induction of controlled hypotension in tympanoplasty. They noted that both the drugs effectively achieved controlled hypotension during surgery with improved surgical conditions.
Similarly, Hamed M et al. compared magnesium sulfate and lidocaine for controlled hypotension in patients undergoing FEES and found that lidocaine provided better surgical field clarity and shorter extubation time.[42]
Few other studies in past have also reported successful use of lidocaine to achieve controlled hypotension.[43] However, more studies with large sample size are needed to establish its role in hypotensive anesthesia.
Newer drugs, like fenoldopam, adenosine and alprostadil, are presently being evaluated for controlled hypotension. However, a higher treatment cost and associated side effects limit their development in this field.
Table 1 Summarizes the commonly used drugs for hypotensive anesthesia.
Table 1.
Commonly used drugs for hypotensive anesthesia
| Drug | Onset time | Duration of action | Side effects | Patient contraindications | Adjustment for special population |
|---|---|---|---|---|---|
| Propofol | 30 sec-1 min | 5–10 min | Propofol infusion syndrome after prolong infusion, bradycardia | Severe renal or hepatic disease | Dose reduction in elderly patients, liver disease, heart failure |
| Remifentanil | 1–3 min | 5–10 min | Respiratory depression (dose-dependent) | Obstructive sleep apnea | Dose reduction in elderly patients, and respiratory disease |
| NTG | 1–2 min | 10–30 min | reflex tachycardia, venous congestion methemoglobinemia and cyanide toxicity (rare) | Patients with increase intracranial tension, Severe anemia | Decrease dose in patients with heart failure, chronic obstructive airway disease (COPD) |
| Labetalol | 2-5 min | 4-8 hours | Bradycardia, heart block | Severe bradycardia, Bronchial asthma, heart block | May have long duration of action in patients with liver and renal dysfunction due to slow metabolism Caution in asthma |
| Esmolol | 1–2 min | 10–20 min | Bradycardia, heart block | Severe asthmatics | Caution in asthma |
| Dexmedetomidine | 5–10 min | 15–30 min | Hypotension, bradycardia, dry mouth, and nausea decrease lacrimation | Current high cost relative to generic medications | In patients with heart block or ventricular dysfunction (ejection fraction <30) – continuous monitoring of ECG, BP, SPO2 is essential |
| Magnesium sulfate | 1–2 min Peak effect within 5-10 min | 30 min-1 h after a single iv dose | Bradycardia, Respiratory depression Muscle weakness | Severe renal impairment Myasthenia gravis Heart block | Reduced dose in renal disease, elderly patient |
| Lidocaine | 3–5 min | 1–2 hours | C.N.S and cardiovascular toxicity | Severe heart block and liver disease | Reduced dose in liver disease, elderly patient |
Non-pharmacological methods
There are several maneuvers to control bleeding. Commonly used is reverse Trendelenburg or head up position where head is reclined 15 degrees from horizontal to allow venous drainage from the surgical field. The blood pressure falls by 2 mm hg for every inch of head raise.[20] However, this technique may be associated with a risk of air embolism. Valsalva maneuver is another method that can help to identify bleeding points, aids in postoperative drainage, and also maintains hemostasis. Pre-donation of autologous blood may decrease the requirement for homologous blood, but this requires extensive preparation and does not reduce the infection risk.[11]
Checklist summarizing the key steps[44]
Preoperative preparation
Thorough knowledge and familiarity of anesthesia team planning the case under hypotensive anesthesia
Check essential investigations, including hemoglobin (Hb), urea, and electrolytes. Ensure minimum Hb of 10g/dL
Adequate premedication can be used to assist induction
ABG sampling in major surgery (both preop and postop)
Ensure patient is normovolumic
Rule out drug allergy
Intraoperative preparation
Ensure smooth induction and intubation
Adequate iv access (especially if plan to start hypotensive agent through infusion)
Maintain adequate depth of anesthesia
Proper padding of pressure areas to prevent skin necrosis
Patient should be positioned with the head elevated about 20º above the heart
Ideally intraarterial blood pressure monitoring should be done
Non-invasive monitoring is sufficient in short and minor surgery
Careful estimation of the blood loss
Discontinue hypotensive anesthesia before wound closure
CONCLUSION
Since each individual is unique, being familiar with the specificity of a patient and modifying anesthesia practice according to his requirements is a component of good anesthesia practice. The hypotensive anesthesia technique is widely used in major maxillofacial surgeries with a high risk of intraoperative bleeding. The decision to induce hypotensive anesthesia should be based according to the general condition of the patient, the extent of the surgery, and in coordination with the operating surgeon. Mere deepening of the anesthesia plane by increasing the concentration of inhalation agents or intravenous agents is not a reasonable practice as it could delay a patient’s arousal from anesthesia and have adverse cardiovascular effects. The target blood pressure should be adjusted according to the patient’s preoperative status and coexisting illness. The risk of organ hypoperfusion should be kept in mind. Close intraoperative monitoring with optimal patient selection is important for good patient outcomes. Other strategies to minimize blood loss can be considered in patients not suitable for hypotensive anesthesia. A risk-benefit analysis should be performed. Once the desired bloodless field is achieved, further drop in blood pressure should be avoided.
Conflicts of interest
There are no conflicts of interest.
Funding Statement
Nil.
REFERENCES
- 1.Barak M, Yoav L, Abu el-Naaj I. Hypotensive anaesthesia versus normotensive anaesthesia during major maxillofacial surgery: A review of the literature. ScientificWorldJournal. 2015;2015:480728. doi: 10.1155/2015/480728. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Gardner WJ. The control of bleeding during operation by induced hypotension. JAMA. 1946;132:572–4. doi: 10.1001/jama.1946.02870450026007. [DOI] [PubMed] [Google Scholar]
- 3.Schaberg SJ, Kelly JF, Terry BC, Posner MA, Anderson EF. Blood loss and hypotensive anesthesia in oral-facial corrective surgery. J Oral Surg. 1976;34:147–56. [PubMed] [Google Scholar]
- 4.Degoute CS. Controlled hypotension: A guide to drug choice. Drugs. 2007;67:1053–76. doi: 10.2165/00003495-200767070-00007. [DOI] [PubMed] [Google Scholar]
- 5.Hu G, Christman J. Alveolar macrophages in lung inflammation and resolution. Front Immunol. 2019;10:2275. doi: 10.3389/fimmu.2019.02275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Barbarisi M, Abbenante D, Piccialli F, Coppolino F, Giaccari L, Pace M, et al. Controlled hypotension in maxillofacial surgery: A commentary. J Oral Maxillofac Anesth. 2023:2. doi: 10.21037/joma-23-6. [Google Scholar]
- 7.Rodrigo C. Induced hypotension during anaesthesia with special reference to orthognathic surgery. Anesth Prog. 1995;42:41–58. [PMC free article] [PubMed] [Google Scholar]
- 8.Kim B, Sangha G, Singh A, Bohringer C. The effect of intraoperative hypotension on postoperative renal function. Curr Anesthesiol Rep. 2023;13:181–6. doi: 10.1007/s40140-023-00564-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Ragupathy K, Baskar R. Hypotensive anaesthesia in orthognathic surgery—A review. J Dent Med Sci. 2015;14:107–9. [Google Scholar]
- 10.Tobias JD. Controlled hypotension in children: A critical review of available agents. Paediatr Drugs. 2002;4:439–53. doi: 10.2165/00128072-200204070-00003. [DOI] [PubMed] [Google Scholar]
- 11.Prasant MC, Kar S, Rastogi S, Hada P, Ali FM, Mudhol A. Comparative study of blood loss, quality of surgical field and duration of surgery in maxillofacial cases with and without hypotensive anaesthesia. J Int Oral Health. 2014;6:18–21. [PMC free article] [PubMed] [Google Scholar]
- 12.Choi WS, Samman N. Risks and benefits of deliberate hypotension in anaesthesia: A systematic review. Int J Oral Maxillofac Surg. 2008;37:687–703. doi: 10.1016/j.ijom.2008.03.011. [DOI] [PubMed] [Google Scholar]
- 13.Drummond JC. Blood pressure and the brain: How low can you go? Anesth Analg. 2019;128:759–71. doi: 10.1213/ANE.0000000000004034. [DOI] [PubMed] [Google Scholar]
- 14.De Blasi RA, Palmisani S, Boezi M, Arcioni R, Collini S, Troisi F, et al. Effects of remifentanil-based general anaesthesia with propofol or sevoflurane on muscle microcirculation as assessed by near-infrared spectroscopy. Br J Anaesth. 2008;101:171–7. doi: 10.1093/bja/aen136. [DOI] [PubMed] [Google Scholar]
- 15.Zhang L, Yu Y, Xue J, Lei W, Huang Y, Li Y, et al. Effect of deliberate hypotension on regional cerebral oxygen saturation during functional endoscopic sinus surgery: A randomized controlled trial. Front Surg. 2021;8:681471. doi: 10.3389/fsurg.2021.681471. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Tang Y, Zhu C, Liu J, Wang A, Duan K, Li B, et al. Association of intraoperative hypotension with acute kidney injury after noncardiac surgery in patients younger than 60 years old. Kidney Blood Press Res. 2019;44:211–21. doi: 10.1159/000498990. [DOI] [PubMed] [Google Scholar]
- 17.Walsh M, Devereaux PJ, Garg AX, Kurz A, Turan A, Rodseth RN, et al. Relationship between intraoperative mean arterial pressure and clinical outcomes after noncardiac surgery: Toward an empirical definition of hypotension. Anesthesiology. 2013;119:507–15. doi: 10.1097/ALN.0b013e3182a10e26. [DOI] [PubMed] [Google Scholar]
- 18.Sun LY, Wijeysundera DN, Tait GA, Beattie WS. Association of intraoperative hypotension with acute kidney injury after elective noncardiac surgery. Anesthesiology. 2015;123:515–23. doi: 10.1097/ALN.0000000000000765. [DOI] [PubMed] [Google Scholar]
- 19.Salmasi V, Maheshwari K, Yang D, Mascha EJ, Singh A, Sessler DI, et al. Relationship between intraoperative hypotension, defined by either reduction from baseline or absolute thresholds, and acute kidney and myocardial injury after noncardiac surgery: A retrospective cohort analysis. Anesthesiology. 2017;126:47–65. doi: 10.1097/ALN.0000000000001432. [DOI] [PubMed] [Google Scholar]
- 20.Rodrigo C. Anesthetic considerations for orthognathic surgery with evaluation of difficult intubation and technique for hypotensive anesthesia. Anesth Prog. 2000;47:151–6. [PMC free article] [PubMed] [Google Scholar]
- 21.Bergstrom C. Controlled hypotension. In: Freeman BS, Berger JS, editors. Anesthesiology Core Review: Part Two Advanced Exam. McGraw-Hill Education; 2016. Available from: https://accessanesthesiology.mhmedical.com/content.aspx?bookid=1750§ionid=117318734 . [Last accessed on 2024 Dec 18] [Google Scholar]
- 22.Piñeiro-Aguilar A, Somoza-Martín M, Gandara-Rey JM, García-García A. Blood loss in orthognathic surgery: A systematic review. J Oral Maxillofac Surg. 2011;69:885–92. doi: 10.1016/j.joms.2010.07.019. [DOI] [PubMed] [Google Scholar]
- 23.Sangkum L, Liu GL, Yu L, Yan H, Kaye AD, Liu H, et al. Minimally invasive or noninvasive cardiac output measurement: An update. J Anesth. 2016;30:461–80. doi: 10.1007/s00540-016-2154-9. [DOI] [PubMed] [Google Scholar]
- 24.Degoute CS, Ray MJ, Manchon M, Dubreuil C, Banssillon V. Remifentanil and controlled hypotension; Comparison with nitroprusside or esmolol during tympanoplasty. Can J Anaesth. 2001;48:20–7. doi: 10.1007/BF03019809. [DOI] [PubMed] [Google Scholar]
- 25.Testa LD, Tobias JD. Pharmacologic drugs for controlled hypotension. J Clin Anesth. 1995;7:326–37. doi: 10.1016/0952-8180(95)00010-f. [DOI] [PubMed] [Google Scholar]
- 26.Patel SS, Goa KL. Sevoflurane. A review of its pharmacodynamic and pharmacokinetic properties and its clinical use in general anaesthesia. Drugs. 1996;51:658–700. doi: 10.2165/00003495-199651040-00009. [DOI] [PubMed] [Google Scholar]
- 27.Rossi A, Falzetti G, Donati A, Orsetti G, Pelaia P. Desflurane versus sevoflurane to reduce blood loss in maxillofacial surgery. J Oral Maxillofac Surg. 2010;68:1007–12. doi: 10.1016/j.joms.2008.12.012. [DOI] [PubMed] [Google Scholar]
- 28.Claeys MA, Gepts E, Camu F. Haemodynamic changes during anaesthesia induced and maintained with propofol. Br J Anaesth. 1988;60:3–9. doi: 10.1093/bja/60.1.3. [DOI] [PubMed] [Google Scholar]
- 29.Ankichetty SP, Ponniah M, Cherian V, Thomas S, Kumar K, Jeslin L, et al. Comparison of total intravenous anesthesia using propofol and inhalational anesthesia using isoflurane for controlled hypotension in functional endoscopic sinus surgery. J Anaesthesiol Clin Pharmacol. 2011;27:328–32. doi: 10.4103/0970-9185.83675. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Giriyapur P, Madhusudhana R. Controlled hypotension for functional endoscopic sinus surgery with two different doses of fentanyl. Cureus. 2023;15:e33859. doi: 10.7759/cureus.33859. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Abu-Sinna RG, Abdelrahman TN. Comparison of the hypotensive efficacy of propofol infusion versus nitroglycerin infusion in functional endoscopic sinus surgery. Ain-Shams J Anesthesiol. 2020;12:65. [Google Scholar]
- 32.Miller M, Kerndt CC, Maani CV. StatPearls. Treasure Island (FL): StatPearls Publishing; 2024. Labetalol. [Updated 2023 Jul 10] Available from: https://www.ncbi.nlm.nih.gov/books/NBK534787/ [Google Scholar]
- 33.Nazir O, Wani MA, Ali N, Sharma T, Khatuja A, Misra R, et al. Use of dexmedetomidine and esmolol for hypotension in lumbar spine surgery. Trauma Mon. 2016;21:e22078. doi: 10.5812/traumamon.22078. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Bajwa SJ, Kaur J, Kulshrestha A, Haldar R, Sethi R, Singh A. Nitroglycerine, esmolol and dexmedetomidine for induced hypotension during functional endoscopic sinus surgery: A comparative evaluation. J Anaesthesiol Clin Pharmacol. 2016;32:192–7. doi: 10.4103/0970-9185.173325. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Shams T, El Bahnasawe NS, Abu-Samra M, El-Masry R. Induced hypotension for functional endoscopic sinus surgery: A comparative study of dexmedetomidine versus esmolol. Saudi J Anaesth. 2013;7:175–80. doi: 10.4103/1658-354X.114073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Turan G, Dincer E, Ozgultekin A, Uslu C, Akgun N. Comparison of dexmedetomidine, remifentanyl and esmolol in controlled hypotensive anaesthesia. Eur J Anaesthesiol. 2008;25:65–6. [Google Scholar]
- 37.El-Gohary MM, Arafa AS. Dexmedetomidine as a hypotensive agent: Efficacy and hemodynamic response during spinal surgery for idiopathic scoliosis in adolescents. Egypt J Anaesth. 2010;26:305–11. [Google Scholar]
- 38.Sajan CR, Soundarya PK, Mohamed A, Krishna PT. A Randomized control trial to compare the efficacy of dexmedetomidine and labetalol for induced hypotensive anesthesia in ear, nose, and throat surgeries. Arch Med Health Sci. 2023;11:37–43. [Google Scholar]
- 39.Goswami D, Yadav P, Bhatt R, Lakshmanan S, Roychoudhury A, Bhutia O. Comparison of efficacy of dexmedetomidine and clonidine infusion to produce hypotensive anesthesia in patients undergoing orthognathic surgery: A randomized controlled trial. J Oral Maxillofac Surg. 2022;80:55–62. doi: 10.1016/j.joms.2021.06.035. [DOI] [PubMed] [Google Scholar]
- 40.Elsharnouby NM, Elsharnouby MM. Magnesium sulphate as a technique of hypotensive anaesthesia. Br J Anaesth. 2006;96:727–31. doi: 10.1093/bja/ael085. [DOI] [PubMed] [Google Scholar]
- 41.Karami A, Fattahi SZ, Hosseini H, Rahmati M, Jahangiri R, Asmarian N, et al. Comparison of labetalol and lidocaine in induction of controlled hypotension in tympanoplasty: A randomized clinical trial. Braz J Otorhinolaryngol. 2024;90:101403. doi: 10.1016/j.bjorl.2024.101403. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Hamed MA. Comparative study between magnesium sulfate and lidocaine for controlled hypotension during functional endoscopic sinus surgery: A randomized controlled study. Anesth Essays Res. 2018;12:715–8. doi: 10.4103/aer.AER_103_18. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Omar AM. Can systemic lidocaine be used in controlled hypotension? A double-blinded randomized controlled study in patients undergoing functional endoscopic sinus surgery. Egypt J Anaesth. 2013;29:295–300. [Google Scholar]
- 44.Shimelis ST, Amare HG, Nurhussen RA. Deliberate hypotension as a mechanism to decrease intraoperative surgical site blood loss in resource limited setting: A systematic review and guideline. Int J Surg Open. 2021;29:55–65. [Google Scholar]
