Back to Search Results

10/1/2018

Fluid Management at Hysteroscopy

Author: Michelle Meglin, MD

Mentor: Ashlyn Savage, MD
Editor: Natalie Bowersox, MD

Registered users can also download a PDF or listen to a podcast of this Pearl.
Log in now, or create a free account to access bonus Pearls features.

During hysteroscopy, systemic absorption of uterine distension fluid occurs largely through disrupted endometrial and myometrial venous sinuses because of the pressure gradient between the uterine cavity and open sinuses or vessels. Higher intrauterine pressure, longer procedure duration, deep myometrial penetration, and large uteri are associated with increased fluid absorption. The lowest intrauterine pressure that provides adequate visualization should be used, and when possible that pressure should be below the mean arterial pressure.

Distension media are categorized by viscosity, tonicity, and electrolyte status. Normal saline is a low viscosity, isotonic solution, with electrolytes, and is best suited for use with bipolar electrocautery or mechanical instruments.  It cannot be used with monopolar electrocautery due to current dispersion by activated ions in the media. Monopolar electrocautery requires use of electrolyte-free fluids including hypotonic (1.5% glycine and 3% sorbitol) and isotonic solutions (5% mannitol).

Excessive absorption of hypotonic electrolyte free fluids, such as 1.5% glycine and 3% sorbitol (less commonly used in current practice), can cause hypo-osmolality, hyponatremia, cerebral edema, hypotonic encephalopathy, permanent neurologic injury, heart failure, pulmonary edema, and death. Careful monitoring of fluids is recommended. While 5% mannitol is less likely to cause hypo-osmolality, it can lead to hyponatremia. Premenopausal women are more likely to have permanent brain damage or die from hyponatremic encephalopathy than post-menopausal women. Excessive absorption of normal saline is not associated with hyponatremia; however, it can cause volume overload, right-sided heart failure, pulmonary edema, and death.

Fluid deficit can be estimated by manual calculation or by use of an automated fluid management system. With manual calculation, the volume of fluid collected in the perineal bag is subtracted from the known quantity infused every 15 minutes during the procedure. There are limitations with manual calculation, so automated fluid management systems that use calibrated electronic weighing scales are preferred.

When using hypotonic solutions, the maximum allowed fluid deficit is 1000mL for healthy patients and 750mL for elderly patients or those with medical comorbidities. For normal saline, the maximum allowed fluid deficit is 2,500mL for healthy patients and 750mL for those with cardiovascular disease. The procedure should be terminated when approaching the allowable fluid deficit.  In the event of a rapid increase in fluid deficit, the occurrence of a uterine perforation should be considered.

Fluid absorption can be reduced by pre-operative treatment with GnRH agonists and intraoperative injection of dilute vasopressin. If excessive absorption of fluid occurs with a hypotonic fluid, serum electrolytes should be obtained, and the patient should be evaluated for volume overload. Asymptomatic hyponatremia can be treated with fluid restriction and careful monitoring of urine output. Treatment of symptomatic hyponatremia requires infusion of 3% sodium chloride (0.5-2mL/kg/hr) and management by a multidisciplinary team including a specialist in intensive care. Fluid overload from normal saline can be managed by fluid restriction; IV furosemide (20-40mg) is indicated if there is clinical or radiological evidence of pulmonary edema.

Further Reading:  

American Association of Gynecologic Laparoscopists, Munro MG, Storz K, et al. AAGL Practice Report: Practice Guidelines for the Management of Hysteroscopic Distending Media. J Minim Invasive Gynecol. 2013 Mar-Apr;20(2):137-48. doi: 10.1016/j.jmig.2012.12.002.

Kho KA. Minimally Invasive Surgery Fundamentals. Williams Gynecology. 4th ed. New York, NY: McGraw-Hill Education LLC. 2020.

Initial Approval:  July 2018. Reaffirmed January 2020; Revised September 2021; Reaffirmed March 2024.

 

********** Notice Regarding Use ************

The Society for Academic Specialists in General Obstetrics and Gynecology, Inc. (“SASGOG”) is committed to accuracy and will review and validate all Pearls on an ongoing basis to reflect current practice.

This document is designed to aid practitioners in providing appropriate obstetric and gynecologic care. Recommendations are derived from major society guidelines and high-quality evidence when available, supplemented by the opinion of the author and editorial board when necessary. It should not be construed as dictating an exclusive course of treatment or procedure to be followed.

Variations in practice may be warranted when, in the reasonable judgment of the treating clinician, such course of action is indicated by the condition of the patient, limitations of available resources, or advances in knowledge or technology. SASGOG reviews the articles regularly; however, its publications may not reflect the most recent evidence. While we make every effort to present accurate and reliable information, this publication is provided “as is” without any warranty of accuracy, reliability, or otherwise, either express or implied. SASGOG does not guarantee, warrant, or endorse the products or services of any firm, organization, or person. Neither SASGOG nor its respective officers, directors, members, employees, or agents will be liable for any loss, damage, or claim with respect to any liabilities, including direct, special, indirect, or consequential damages, incurred in connection with this publication or reliance on the information presented.

Copyright 2024 The Society for Academic Specialists in General Obstetrics and Gynecology, Inc. All rights reserved.  No re-print, duplication or posting allowed without prior written consent.

 

Back to Search Results