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Anesthesia Management in Patients Undergoing Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy

S

Sanliurfa Mehmet Akif Inan Education and Research Hospital

Status

Completed

Conditions

Hyperthermic Intraperitoneal Chemotherapy
Cytoreductive Surgery
Anesthesia

Study type

Observational

Funder types

Other

Identifiers

NCT06398678
MAIEAHANEST

Details and patient eligibility

About

A combined approach of cytoreductive surgery (SRC) and hyperthermic intraperitoneal chemotherapy (HIPEC) represents a potential treatment option for patients diagnosed with primary or secondary gastrointestinal or gynaecological malignancies with peritoneal involvement. While the surgical phase of the operation macroscopically addresses the cancerous tissue, the HIPEC phase targets the microscopic tumour cells that remain after surgery (1). The surgical procedure known as SRC and HIPEC is one of the most complex surgical procedures, presenting numerous challenges for both the surgical and anaesthesia teams. The haemodynamic, haematological and metabolic changes that occur before, during and in the early postoperative period are associated with an increased risk of morbidity and mortality. It is therefore crucial for anaesthesia management to maintain normovolemia during surgery, compensate for hypothermia in the surgical phase and hyperthermia in the HIPEC phase, and maintain metabolic and haemodynamic balance throughout the entire procedure.

The objective of this study was to retrospectively examine the anaesthesia management and clinical outcomes in patients who underwent cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC) in order to create literature information that can facilitate the early recognition and prevention of haemodynamic, haematological and metabolic problems that occur especially in the intraoperative and postoperative period.

Enrollment

50 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with primary or secondary gastrointestinal or gynecologic malignancies with peritoneal involvement.
  • Over 18 years of age

Exclusion criteria

  • Over 80 years of age
  • those with heart, lung and liver diseases

Trial design

50 participants in 1 patient group

Patients who had undergone cytoreductive surgery.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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