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Dexamethasone for Post-cesarean Delivery Pain

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Sponsor
Duke University

Parole chiave

Astratto

The purpose of this study is to compare post-cesarean section consumption of pain medication between two groups of patients undergoing scheduled cesarean section at term gestation who receive a single-dose of intraoperative steroid (dexamethasone 8 milligrams) versus placebo at 24 hours after surgery. The hypothesis is that a single perioperative dose of dexamethasone 8 mg will significantly reduce postoperative opioid consumption at 24 h in women having cesarean delivery under spinal anesthesia.

Descrizione

Steroids have been used to reduce inflammation and tissue damage in a variety of conditions, have potent immunomodulatory effects, and are a mainstay in the treatment of acute allograft rejection. Dexamethasone has been shown to be a safe and effective anti-emetic therapy for patients undergoing cesarean section surgery with spinal anesthesia containing morphine.

However, recent evidence suggests that dexamethasone may also play a role in reducing post-operative pain and opioid consumption. Early studies in patients undergoing dental procedures showed that glucocorticoids were effective in reducing postoperative pain and edema. Multiple recent studies have also investigated the potential analgesic benefit of a single perioperative dose of dexamethasone, but the results have been inconsistent. The effect of single-dose, intraoperative, intravenous dexamethasone therapy on post-operative pain and opioid consumption has not yet been studied in patients undergoing cesarean section.

Pain is a significant source of morbidity for many women following cesarean section, and has serious consequences beyond the immediate post-operative period. Patients with poorly-controlled pain may have difficulty with ambulation that can lead to atelectasis, pneumonia, and venous thromboembolism.

Poor maternal pain control may also affect the infant by interfering with bonding and breastfeeding. Reduction of post-operative opioid consumption is desirable because it may also reduce the incidence of opioid-induced side effects such as sedation, constipation, nausea, vomiting and pruritus. Some evidence suggests that the severity of post-operative pain following cesarean section may predict progression to chronic pain, and postpartum depression.

Although 10 to 18% of women who undergo cesarean section will experience chronic pain following surgery, it is difficult to predict those patients who will experience this complication. Recent investigations have shown that patient responses to standardized painful stimuli prior to surgery help predict severity of post-operative pain and possibly progression to chronic pain. This type of information could potentially help to tailor the clinical management of patients at risk for severe and/or chronic post-operative pain to improve outcomes for these patients. Landau and colleagues have described a simple and minimally-invasive method of assessing response to noxious stimuli using a von-Frey filament to obtain a mechanical temporal summation score.

Date

Ultimo verificato: 05/31/2017
Primo inviato: 03/12/2013
Iscrizione stimata inviata: 03/12/2013
Primo pubblicato: 03/14/2013
Ultimo aggiornamento inviato: 06/25/2017
Ultimo aggiornamento pubblicato: 07/24/2017
Data dei primi risultati presentati: 05/24/2017
Data dei primi risultati QC presentati: 06/25/2017
Data dei primi risultati pubblicati: 07/24/2017
Data di inizio effettiva dello studio: 11/30/2012
Data di completamento primaria stimata: 05/26/2016
Data stimata di completamento dello studio: 09/20/2016

Condizione o malattia

Pain, Postoperative
Postoperative Nausea and Vomiting

Intervento / trattamento

Drug: Dexamethasone

Drug: Placebo

Fase

Fase 4

Gruppi di braccia

BraccioIntervento / trattamento
Experimental: Dexamethasone
Dexamethasone 8 mg IV given intraoperatively as a one-time dose.
Drug: Dexamethasone
Dexamethasone 8 mg IV (as a one time dose)
Placebo Comparator: Placebo
Sodium chloride 0.9% (5 ml) given IV intraoperatively as a one time dose.
Drug: Placebo
Sodium Chloride 0.9% -5 ml

Criteri di idoneità

Età idonea per lo studio 18 Years Per 18 Years
Sessi idonei allo studioFemale
Accetta volontari sani
Criteri

Inclusion Criteria:

- American Society of Anesthesiology (ASA) class 1, 2 and 3

- Gestational age > 37 weeks

- scheduled for elective cesarean delivery

- spinal or combined spinal epidural anesthesia

- 18 years or older

- speak English

Exclusion Criteria:

- BMI > 45 kg/m2

- Diabetes Mellitus (Type 1, 2 and gestational)

- mild or severe preeclampsia

- history of intravenous drug or opioid abuse

- previous history of chronic pain syndrome

- history of opioid use in the past week

- receipt of an antiemetic within 24 h prior to surgery

- Non-English speaking

Risultato

Misure di esito primarie

1. Morphine Consumption at 24 Hours Post-op [24 hours from admission to Postanesthesia care unit (PACU)]

The primary outcome will be the cumulative morphine consumption at 24 h in the two study groups. All postoperative opioids were converted to IV morphine equivalents using the following conversion factors: 100 micrograms IV = 10 mg IV morphine, 20 mg oxycodone po = 10 mg IV Morphine

Misure di esito secondarie

1. Pain Scores Between the Groups at 2 Hours. [2 hours from admission to postanesthesia care unit (PACU)]

Pain scores were measured using a numeric rating scale with a range from 0 to 10, with 0 meaning no pain and 10 indicating the most severe pain.

2. Time to Administration of First Rescue Analgesic Request Between the Groups. [PACU admission to discharge from PACU an average of 2 hours]

Time in minutes from admission to PACU to the first request by the patient for oral oxycodone (analgesia) administration for pain

3. Cumulative Opioid Consumption at 48 Hours Between the Groups [Admission to PACU through 48 hours]

The secondary outcome was the cumulative morphine consumption at 48 h in the two study groups. All postoperative opioids were converted to IV morphine equivalents using the following conversion factors: 100 micrograms IV = 10 mg IV morphine, 20 mg oxycodone po = 10 mg IV Morphine

4. Pain Scores Between the Groups at 24 Hours. [24 hours from PACU admission]

Pain scores were measured using a numeric rating scale with a range from 0 to 10, with 0 meaning no pain and 10 indicating the most severe pain.

5. Pain Scores Between the Groups at 48 Hours. [48 hours from PACU Admission]

Pain scores were measured using a numeric rating scale with a range from 0 to 10, with 0 meaning no pain and 10 indicating the most severe pain.

6. Cumulative Opioid Consumption at 24 Hours Between MTS Groups [24 hours from admission to Postanesthesia care unit (PACU)]

Mechanical temporal summation (MTS) was assessed using A 180 g Von Frey Filament was applied to the volar aspect of the dominant forearm, and subjects were asked to rate pain scores (NRS 0-100, 0 = no pain and 100= worst pain possible) after the 1st and 11th tap. A difference < 1 was recorded as MTS negative, and a difference > or = 1 was recorded as MTS positive.

7. Incidence of Chronic Persistent Pain at 8 Weeks [8 weeks from the day of surgery]

Patients answered a questionnaire at 8 weeks to determine whether they still had persistent surgical site pain 8 weeks following surgery

8. Incidence of Chronic Persistent Pain at 6 Months [6 months from the day of surgery]

Patients answered a questionnaire at 6 months to determine whether they still had persistent surgical site pain 6 months following surgery

9. Pain Scores Between MTS Groups [24 hours after PACU admission]

Mechanical temporal summation (MTS) was assessed using A 180 g Von Frey Filament was applied to the volar aspect of the dominant forearm, and subjects were asked to rate pain scores (NRS 0-100, 0=no pain and 100=worst pain possible) after the 1st and 11th tap. A difference < 1 was recorded as MTS negative, and a difference > or = 1 was recorded as MTS positive.

10. Incidence of Intraoperative Nausea and Vomiting (IONV) and Need for Rescue Antiemetics. [From spinal anesthesia placement to end of surgery, approximately 70 minutes]

Incidence of intraoperative nausea and vomiting and need for rescue antiemetics were recorded during surgery. Patient who reported a nausea score on a 11 point NRS where 0=no nausea and 10 = the worse nausea possible. Patients who retched or vomited were reported to have vomited. Patients receiving any antiemetic during surgery were recorded as those requesting ( needing) rescue antiemetic.

11. Incidence of Intraoperative Pruritus [From spinal anesthesia placement to end of surgery, approximately 70 minutes]

pruritus was defined as patients reporting a pruritus score of greater than o on a numerical rating scale with o=no pruritus and 10= worst pruritus

12. Incidence of Postoperative Pruritus [48 hours from admission to PACU]

Incidence of postoperative pruritus was calculated based on their postoperative pruritus scores measured at 2 hours, 24 hours and 48 hours. Median of the scores recorded at three time points was calculated. If median score >0 then patient experienced postoperative pruritus.

13. Need for Intraoperative Analgesic Supplementation [From spinal anesthesia placement to end of surgery, approximately 70 minutes]

Need for intraoperative analgesic supplementation was determined by patients who required intraoperative analgesics for pain

14. Incidence of Post-operative Nausea and Vomiting (PONV) and Need for Rescue Antiemetics [2, 24 and 48 hours from PACU admission]

Patients who had experienced Postoperative nausea either reported postoperative nausea scores at 2, 24 and 48 hours from >0, reported an episode of vomiting or received an antiemetic were recorded as experiencing PONV. Patients who received at least one rescue antiemetic postoperatively were recorded as requiring a rescue antiemetic

15. Incidence of Wound Complications [24 hours from PACU admission]

Patients were assessed for signs of surgical wound inspection by the obstetric team following surgery

16. Blood Pressure Measurements Obtained by the Standard of Care Non-invasive Blood Pressure Monitor Compared With the Continuous Noninvasive Arterial Pressure (CNAP) [Intraoperatively]

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