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Is Permissive Hypotension Truly Harmless? Early Biomarker Evidence of Subclinical Kidney Injury in Rhinologic Surgery

Relationship Between Permissive Hypotension and Acute Kidney Injury in Rhinologic Surgeries: Evaluation With Serum NGAL and Cystatin C Levels

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07328620
Enrollment
35
Registered
2026-01-09
Start date
2025-03-01
Completion date
2025-07-30
Last updated
2026-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury, Hypotension

Keywords

Permissive Hypotension, Subclinical Kidney Injury, NGAL, Cystatin C, Rhinologic Surgery, Surgical Field Visibility, Boezaart Score

Brief summary

This study aims to investigate the effects of permissive hypotension, which is routinely used in rhinologic surgeries such as rhinoplasty, septoplasty, and functional endoscopic sinus surgery (FESS), on renal function. Although permissive hypotension has been widely practiced to improve surgical field visibility and reduce intraoperative blood loss, its specific definition is not standardized in the literature. In most studies, maintaining mean arterial pressure (MAP) within the range of 50-65 mmHg is considered permissive hypotension. MAP values below 60 mmHg have been associated with increased risk of cardiac and renal complications. However, in otherwise healthy patients, such episodes are frequently tolerated without clinically apparent renal dysfunction. The kidneys have a strong compensatory reserve capacity, and early tubular injury may not be detected by conventional renal function tests such as serum creatinine. Therefore, the use of more sensitive biomarkers is necessary to detect potential subclinical injury. In this prospective observational study, serum NGAL and cystatin C levels will be measured from routine preoperative and postoperative (12-24 hours) blood samples obtained from adult patients undergoing rhinologic procedures. A ≥25% increase in these biomarkers from baseline will be considered indicative of subclinical acute kidney injury. Additionally, intraoperative hemodynamic data will be monitored, and the duration of MAP \<60 mmHg and MAP \<65 mmHg will be recorded. At the end of the procedure, surgical field conditions will be evaluated using the Boezaart Surgical Field Score. The relationship between these parameters and biomarker changes will be analyzed. The goal of this study is to determine whether early, clinically silent renal injury may occur during permissive hypotension and to provide insight into its potential implications for future renal function. All interventions and blood samplings are part of routine care, and no additional procedures will be performed for research purposes.

Detailed description

Permissive hypotension is a commonly used anesthetic technique in rhinologic surgeries to optimize surgical conditions by reducing bleeding and improving visualization. Although widely applied, a standardized definition is lacking in the literature. Many studies define permissive hypotension as maintaining mean arterial pressure (MAP) between 50-65 mmHg. MAP values lower than 60 mmHg may compromise tissue perfusion and oxygenation, particularly in the renal medulla, possibly predisposing patients to ischemic stress. Despite this, in patients without significant comorbidities, these controlled reductions typically do not result in clinically evident kidney dysfunction, which supports the continued use of this technique in suitable cases. However, due to the high renal reserve, subclinical kidney injury may still occur without notable changes in serum creatinine or urine output. The early detection of renal injury may be possible through biomarkers such as neutrophil gelatinase-associated lipocalin (NGAL) and cystatin C, which are more sensitive to structural renal injury. This study is designed to evaluate such potential biomarker changes during permissive hypotension applied for rhinologic surgery. Study Design and Methods: This is a prospective observational, single-center study including 35 adult patients aged 18-65 years who are scheduled to undergo elective rhinoplasty, septoplasty, or FESS. Patients with a history of chronic kidney disease, uncontrolled hypertension or diabetes mellitus, or contraindications to hypotensive anesthesia will be excluded. Informed consent will be obtained preoperatively. All blood sampling and hemodynamic monitoring will be performed as part of routine clinical care, and no additional intervention will be introduced. Data Collection and Measurements: Preoperative routine blood samples will be analyzed for renal biomarkers including serum NGAL and cystatin C, in addition to standard biochemistry profiles. Serum NGAL levels will be measured using a validated ELISA method (Elabscience, USA), and serum cystatin C levels will be analyzed using the Siemens Atellica Neph 630 analyzer with a nephelometric method. Intraoperative hemodynamic variables will be recorded every 5 minutes throughout anesthesia, and total durations of MAP \<60 mmHg and MAP \<65 mmHg will be calculated. Postoperatively, between 12 and 24 hours, routine blood sampling will again be performed, and NGAL and cystatin C levels will be re-evaluated. At the end of surgery, surgical field visibility will be assessed by the otorhinolaryngology surgical team using the Boezaart Surgical Field Score. Outcome Measures: The primary outcome of this study is the presence of subclinical renal injury, defined as a ≥25% increase in plasma NGAL and/or cystatin C from preoperative baseline to the postoperative 12-24-hour measurement. Secondary outcomes include the association between biomarker changes and intraoperative hypotension exposure (duration of MAP \<60 mmHg and MAP \<65 mmHg), as well as the relationship between hypotension and surgical field quality assessed with the Boezaart Score. Safety and Adverse Event Monitoring: All procedures are routine clinical practices and carry no additional risk to participants. In the event of postoperative impairment of renal function, standard clinical management will be followed, including fluid optimization and nephrology consultation when appropriate. Data Confidentiality: All collected data will be de-identified and stored securely with restricted access limited to the research team.

Interventions

None listed

Sponsors

Gazi University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults aged 18-65 years * Scheduled for elective rhinologic surgery (rhinoplasty, septoplasty, or functional endoscopic sinus surgery) * ASA physical status I-II * Able to provide written informed consent * Undergoing controlled hypotension anesthesia as part of routine clinical management

Exclusion criteria

* Known chronic kidney disease (baseline creatinine above normal range or documented CKD) * Uncontrolled hypertension or uncontrolled diabetes mellitus * Contraindications to controlled hypotensive anesthesia * Pregnant or breastfeeding women * History of major cardiovascular disease affecting renal perfusion (e.g., severe heart failure) * Use of nephrotoxic medications preoperatively that may interfere with renal biomarker interpretation * Perioperative complications requiring deviation from routine anesthetic management (e.g., major bleeding or hemodynamic instability)

Design outcomes

Primary

MeasureTime frameDescription
Change in serum NGAL and cystatin C concentrations indicating biomarker-defined subclinical renal stressPreoperative baseline to postoperative 12-24 hoursSerum NGAL concentration (ng/mL) measured by ELISA assay and serum cystatin C concentration (mg/L) measured by automated nephelometric assay will be assessed preoperatively and at postoperative 12-24 hours. A relative increase of ≥25% from baseline will be used as an interpretive biomarker threshold, primarily for NGAL and more cautiously for cystatin C.

Secondary

MeasureTime frameDescription
Duration of mean arterial pressure below 60 mmHg during anesthesiaIntraoperative periodThe total duration (minutes) of intraoperative mean arterial pressure (MAP) \<60 mmHg recorded at 5-minute intervals from standard anesthesia monitoring.
Duration of mean arterial pressure below 65 mmHg during anesthesiaIntraoperative periodThe total duration (minutes) of intraoperative mean arterial pressure (MAP) \<65 mmHg recorded at 5-minute intervals from standard anesthesia monitoring.
Correlation between intraoperative hypotension duration and renal biomarker changesIntraoperative period to postoperative 12-24 hoursCorrelation between cumulative duration of MAP \<60 mmHg and \<65 mmHg (minutes) and percentage change in serum NGAL (ng/mL) and cystatin C (mg/L) concentrations from baseline.
Correlation between surgical field quality and intraoperative hypotensionEnd of surgeryCorrelation between Boezaart Surgical Field Score (0-5 scale) and cumulative duration of MAP \<60 mmHg and \<65 mmHg (minutes).

Countries

Turkey (Türkiye)

Contacts

STUDY_DIRECTORHasan K Pampal, M.D.

Gazi University Faculty of Medicine, Department of Anesthesiology and Reanimation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 5, 2026