Hemodynamic Effects of Surgical Position in Prone vs. Supine Percutaneous Nephrolithotomy
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Prone Position Percutaneous Nephrolithotomy, Supine Position Percutaneous Nephrolithotomy (Galdakao-modified Valdivia).
- Кому может быть актуально
- Состояния в реестре: Percutaneous Nephrolithotomy (PCNL), Surgical Positioning, Prone Position, Supine Position. Базовые параметры: 18 лет — 80 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Turkey (Türkiye)
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
The Effect of Surgical Position on Hemodynamics in Percutaneous Nephrolithotomy Performed in Prone and Supine Positions
Обзор
This prospective, randomized controlled study evaluates the hemodynamic effects of prone and supine positions during percutaneous nephrolithotomy (PNL) for large kidney stones. Surgical position may influence intraoperative and postoperative hemodynamic stability. Prone positioning can increase intrathoracic pressure and reduce venous return, whereas supine positioning may provide greater hemodynamic stability. A total of 84 patients will be randomized to undergo PNL in prone or supine positions. Primary outcomes include changes in hemodynamic parameters during surgery. Results may guide surgical position selection, especially in patients with potential hemodynamic risk.
Подробное описание
Percutaneous nephrolithotomy (PNL) is a widely used minimally invasive surgical technique for the treatment of large and complex renal calculi. Traditionally, PNL has been performed in the prone position; however, the supine position has gained popularity in recent years due to potential anesthetic and surgical advantages. Surgical positioning can significantly influence cardiovascular and respiratory function, potentially leading to intraoperative and postoperative hemodynamic fluctuations.
Previous literature suggests that the prone position may increase intrathoracic pressure and impair venous return, potentially compromising hemodynamic stability, while the supine position may provide a more stable cardiovascular profile. However, existing data are limited, and results remain inconclusive, particularly in direct comparative studies.
This prospective, randomized controlled clinical trial aims to compare the effects of prone and supine positions during PNL on patients' intraoperative and postoperative hemodynamic parameters. The study will enroll 84 patients aged 18-80 years with American Society of Anesthesiologists (ASA) physical status I-III undergoing elective PNL. Patients will be randomly assigned to either the prone (n=42) or supine (n=42) position.
Inclusion criteria include patients with renal calculi suitable for PNL and meeting the study's eligibility requirements. Exclusion criteria include pregnancy, uncontrolled coagulopathy, previous renal surgery, severe cardiac, pulmonary, or neurological disease, preoperative urinary tract infection, surgery duration outside 60-120 minutes, and multiple access tracts.
Preoperative evaluation will include demographic data, stone characteristics, and relevant laboratory and imaging findings. Intraoperative data will include systolic and diastolic blood pressure, heart rate, arterial blood gas analysis, operative time, anesthesia duration, access details, irrigation volume, and any transfusion or complications. Postoperative parameters will include nephrostomy duration, length of hospital stay, and presence of residual stones as assessed by postoperative CT scan.
Surgical techniques will be standardized for both positions. Prone PNL will involve initial lithotomy positioning for ureteral catheter placement followed by prone positioning for renal access under fluoroscopic guidance. Supine PNL will be performed in the Galdakao-modified Valdivia position with similar access and fragmentation protocols.
The primary outcome is the difference in intraoperative and postoperative hemodynamic stability between positions. Secondary outcomes include complication rates, residual stone rates, and hospital stay duration.
This study aims to provide high-quality evidence to guide surgeons and anesthesiologists in selecting the optimal patient position for PNL, particularly in individuals with higher hemodynamic risk.
Вмешательства
- Процедура Prone Position Percutaneous Nephrolithotomy
Patients in this arm will undergo percutaneous nephrolithotomy (PNL) in the prone position. The procedure begins with ureteral catheter placement in lithotomy position, followed by prone positioning for renal access under C-arm fluoroscopic guidance. Stone fragmentation will be performed using pneumatic or ultrasonic lithotripters, and nephrostomy placement will be completed according to standard protocol. - Процедура Supine Position Percutaneous Nephrolithotomy (Galdakao-modified Valdivia)
Patients in this arm will undergo percutaneous nephrolithotomy (PNL) in the Galdakao-modified Valdivia supine position. Following general anesthesia, the ipsilateral side will be elevated 20-30°, with the ipsilateral leg extended and the contralateral leg abducted. Ureteral catheter placement will be followed by renal access under C-arm fluoroscopy. Stone fragmentation and removal will be performed using the same standardized lithotripsy and irrigation protocols as in the prone group.
Первичные конечные точки
- Change in Hemodynamic Parameters (Intraoperative) [Срок оценки: From induction of anesthesia to the end of surgery (approximately 60-120 minutes)]
- Change in Arterial Blood pH [Срок оценки: Preoperative, intraoperative, postoperative day 1]
- Change in Diastolic Blood Pressure (Intraoperative) [Срок оценки: From induction of anesthesia to the end of surgery (approximately 60-120 minutes]
- Change in Mean Arterial Pressure (Intraoperative) [Срок оценки: From induction of anesthesia to the end of surgery (approximately 60-120 minutes)]
- Change in Heart Rate (Intraoperative) [Срок оценки: From induction of anesthesia to the end of surgery (approximately 60-120 minutes)]
- Change in Arterial pO₂ [Срок оценки: Preoperative, intraoperative, postoperative day 1]
- Change in Arterial HCO₃- [Срок оценки: Preoperative, intraoperative, postoperative day 1]
- Change in Oxygen Saturation [Срок оценки: Preoperative, intraoperative, postoperative day 1]
- Change in Arterial pCO₂ [Срок оценки: Preoperative, intraoperative, postoperative day 1]
Вторичные конечные точки (7)
- Operative Time [Срок оценки: From initial skin incision until completion of stone removal (approximately 30-180 minutes).]
- Anesthesia Duration [Срок оценки: From induction of anesthesia until termination of anesthesia and awakening of the patient (approximately 60-240 minutes).]
- Intraoperative Blood Loss [Срок оценки: Intraoperative period (from skin incision to completion of surgery, approximately 30-180 minutes).]
- Complication Rate [Срок оценки: From intraoperative period through hospital stay and up to 30 days postoperatively.]
- Residual Stone Rate [Срок оценки: At postoperative 1 month, assessed by CT scan.]
- Length of Hospital Stay [Срок оценки: From hospital admission until discharge (typically 2-10 days).]
- Nephrostomy Tube Duration [Срок оценки: From postoperative day 0 (day of surgery) until nephrostomy tube removal, typically within 7-14 days.]
Критерии участия
Критерии включения
- ASA physical status I-III
- Presence of renal calculi indicated for PNL
Критерии исключения
- Pregnancy
- Uncontrolled coagulopathy
- Previous renal surgery
- Severe cardiac, pulmonary, or neurological disease
- Preoperative urinary tract infection (non-sterile urine culture)
- Surgery duration <60 minutes or >120 minutes
- Preoperative blood transfusion
- Multiple access tracts
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
Turkey (Türkiye) · 1 центр
- Gaziosmanpaşa Training and Research Hospital — Istanbul
Идентификаторы
NCT: NCT07138872 · AIBU-SBF-ABK-01