A randomized trial of crystalloid versus colloid solution for prevention of hypotension during spinal or low-dose combined spinal-epidural anesthesia for elective cesarean delivery

International Journal of Obstetric Anesthesia

Volumn 16, Issue 1, 2007, Pages 8-12

  Ko, J S ^a   Kim, C S ^a   Cho, H S ^a   Choi, D H ^a  

^a Sungkyunkwan University School of Medicine   (South Korea)

Author keywords

Cesarean delivery; Colloid; Combined spinal epidural anesthesia; Crystalloid; Preload; Spinal anesthesia

Indexed keywords

BUPIVACAINE; EPHEDRINE; FENTANYL; HETASTARCH; RINGER LACTATE SOLUTION;

ADULT; ARTICLE; CESAREAN SECTION; CHRONOTHERAPY; CLINICAL TRIAL; COLLOID; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CRYSTALLOID; DOUBLE BLIND PROCEDURE; ELECTIVE SURGERY; EPIDURAL ANESTHESIA; FEMALE; HUMAN; HYPOTENSION; INCIDENCE; INTERMETHOD COMPARISON; LOW DRUG DOSE; MAJOR CLINICAL STUDY; NAUSEA; NAUSEA AND VOMITING; RANDOMIZED CONTROLLED TRIAL; SPINAL ANESTHESIA; SYMPTOM;

ADULT; ANALYSIS OF VARIANCE; ANESTHESIA, EPIDURAL; ANESTHESIA, SPINAL; ANESTHETICS, COMBINED; BUPIVACAINE; CESAREAN SECTION; DOUBLE-BLIND METHOD; FEMALE; FENTANYL; HETASTARCH; HUMANS; HYPOTENSION; ISOTONIC SOLUTIONS; NAUSEA; PREGNANCY; PROSPECTIVE STUDIES;

EID: 33845442877     PISSN: 0959289X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijoa.2006.07.004     Document Type: Article

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