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Effect of Neuromuscular Block and Arterial PCO2 on Surgical Rating Scale (SRS), Following Reversal With Sugammadex

Effect of Deep Neuromuscular Block and Variations in Arterial PCO2 on the Surgical Rating Scale (SRS), Extubation Conditions and Postoperative Conditions Following Reversal With Sugammadex

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01968447
Acronym
BLISSS2
Enrollment
40
Registered
2013-10-24
Start date
2014-02-28
Completion date
2015-10-31
Last updated
2020-03-16

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

Conditions

Prostate Cancer, Renal Cancer

Brief summary

The purpose of this study is to study the effect of variations in the arterial CO2 concentration during deep neuromuscular block on the surgical conditions as assessed by the surgical rating scale

Detailed description

Surgical conditions in laparoscopic surgery are largely determined by the depth of neuromuscular relaxation during surgery. This is especially true in procedures which are confined to a narrow working field such as retroperitoneal laparoscopic surgery (eg. renal and prostatic surgery). In the previous study (BLISS study) deep neuromuscular block (NMB) has shown to provide superior surgical conditions compared to moderate NMB. Moreover, rapid reversal of a deep NMB at the end of surgery was possible with Sugammadex (4mg/kg). The deep NMB did not lead to any delay in extubation time and did not cause any prolongation of stay in the recovery room when the block was reversed with Sugammadex Rapid, safe and complete reversal of profound NMB blockade was not possible until the discovery of Sugammadex. Sugammadex is a modified γ-cyclodextrin. It was developed to selectively bind free plasma rocuronium, a non-depolarizing steroidal neuromuscular blocking agent. The BLISS study was the first study in which the effect of deep NMB on surgical conditions was assessed. Surgical conditions in this study were scored by one surgeon on a newly applied surgical rating scale which ranges from one to five. Although the BLISS study showed that a deep NMB provided better surgical conditions than a moderately deep NMB overall, there was a high variability in surgical rating scores. More over, even at the deep NMB, SRS scores of 3 (moderate, but acceptable conditions) were noted. This indicates that surgical conditions are influenced by other factors as well. Involuntary movement of the diaphragm is possibly such a major disturbant of the surgical field. Previous studies have shown a relative resistance to neuromuscular blocking agents of the diaphragm compared to the musclus adductor pollicis on which neuromuscular block is generally monitored. Hence contractions of the diaphragm may occure despite a deep NMB. This may be due to (high) arterial carbon dioxide (CO2) concentrations, which stimulate the respiratory neuronal pool in the brainstem and consequently activate the phrenic nerve. In normal circumstances, the respiratory centers try to maintain an arterial CO2 pressure of 40 mmHg. With intentional hyperventilation, the arterial CO2 pressure may be lowered to 10-20 mmHg. A low arterial CO2 pressure diminishes the respiratory drive and consequently phrenic nerve activity. This is supported by previous observations which showed increased abdominal muscle relaxation produced by hyperventilation. We therefore designed this study to evaluate the effect of arterial CO2 variation with concurrent deep NMB on the surgical conditions. Arterial CO2 tensions may be altered by adjusting the ventilator settings. Eg. by increasing minute ventilation volume, arterial CO2 concentration will lower. Regular arterial blood samples will be drawn to monitor arterial CO2 concentration. We hypothesize that a Deep NMB combined with hypocapnia will result in a significant improvement of surgical conditions as rated on the surgical rating scale by one surgeon compared to deep NMB and normocapnia Additional secondary end-points of the study include the effect of arterial CO2 variation on: * economic parameters (time to spontaneous breathing, time to extubation, duration of surgery, and time in the post-anesthesia care unit) * perioperative hemodynamics, abdominal pressure * postoperative conditions (respiratory conditions, hemodynamics, arterial oxygen saturation, pain, sedation, nausea and vomiting) * To assess the ability of anesthesiologists and surgeons to rate the surgical field using video snippets of the surgical field.

Interventions

OTHERhypocapnia

Hyperventilation to the level of hypocapnia

Normal ventilation to the level of nromocapnia

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
Leiden University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* (i) Patients diagnosed with renal or prostatic disease who are will undergo an elective laparoscopic renal surgical procedure or laparoscopic prostatectomy; * (ii) ASA class I-III * (iii) \> 18 years of age; * (iv) Ability to give oral and written informed consent.

Exclusion criteria

* (i) Known or suspected neuromuscular disorders impairing neuromuscular function; * (ii) Allergies to muscle relaxants, anesthetics or narcotics; * (iii) A (family) history of malignant hyperthermia; * (iv) Women who are or may be pregnant or are currently breast feeding; * (v) Renal insufficiency, as defined by serum creatinine x 2 of normal, or urine output \< 0.5 ml/kg/h for at least 6 h. When available, other indices will be taken into account as well such as glomerular filtration rate \< 60 ml/h and proteinuria (a ratio of 30 mg albumin to 1 g of creatinine). * (vi) Previous retroperitoneal surgery at the site of the current surgery. * (vii) Body mass index \> 35 kg/m2 * (viii) Chronic obstructive pulmonary disease GOLD 2-4 or a FEV1 less than 70% predicted or VC less than 70% predicted * (ix) chronic pulmonary disease with altered lung physiology (eg. sarcoidosis, cycstic fibrosis, obstructing pulmonary tumors, previous lung surgery)

Design outcomes

Primary

MeasureTime frameDescription
Surgical Rating ScalePeroperativeDuring a procedure, the surgical condition will be scored by one surgeon using a 5-point surgical rating scale. The rating scale is a 5-point ordinal scale ranging from 1 = poor condition to 5 = optimal surgical conditions. The surgeon will score the condition at 15 minute intervals.The values given on the surgical rating scale are averaged and the average value is used in the data analysis.

Secondary

MeasureTime frameDescription
Respiratory Functionfrom the end of surgery untill 2 hours postoperativeThe effect of low versus normal pCO2 concentrations on the postoperative respiratory function will be studied. Postoperative saturations are obtained at 15 minutes intervals. The data are averaged over time.
Pain Intensity on an 11-point Scale in the Postoperative Periodfrom the end of surgery untill 2 hours postoperativeThe effect of low versus normal pCO2 concentrations on postoperative pain will be studied. Painscores are obtained at 15 minutes intervals and are expressed as a number on a 10 point scale (numeric rating scale; 1 (low)-10(maximum)). The data is avaraged over time
HemodynamicsperoperativeHemodynamic conditions are studied during low arterial CO2 concentration and normal arterial CO2 concentration. The average of the measured mean arterial pressures at 15 minute intervals during anesthesia are presented
Nauseafrom the end of surgery untill 2 hours postoperativeThe effect of low versus normal pCO2 concentrations on the incidence of postoperative nausea will be studied. The incidence is expressed as the percentage of people experiencing nausea per arm.
Vomitingfrom the end of surgery untill 2 hours postoperativeThe effect of low versus normal pCO2 concentrations on the incidence of postoperative vomiting will be studied. The incidence of vomiting is expressed as a precentage of the patients per arm.
Sedationfrom the end of surgery untill 2 hours postoperativeThe effect of low versus normal pCO2 concentrations on postoperative sedation will be studied using the using the validated Leiden Observer's Assessment of Alertness/Sedation (0 (awake) - 6 (unarousable)) scale at 15 min intervals. The data are averaged over time.

Countries

Netherlands

Participant flow

Participants by arm

ArmCount
Hypocapnia
arterial pCO2 of 3.5 kPa or 26.3 mmHg hypocapnia
20
Normocapnia
arterial PCO2 of 6.5-7.0 kPa or 48.8-52.5 mmHg normocapnia
20
Total40

Baseline characteristics

CharacteristicNormocapniaHypocapniaTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
8 Participants10 Participants18 Participants
Age, Categorical
Between 18 and 65 years
12 Participants10 Participants22 Participants
Age, Continuous62 years65 years64 years
Region of Enrollment
Netherlands
20 participants20 participants40 participants
Sex: Female, Male
Female
6 Participants3 Participants9 Participants
Sex: Female, Male
Male
14 Participants17 Participants31 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 200 / 20
serious
Total, serious adverse events
0 / 200 / 20

Outcome results

Primary

Surgical Rating Scale

During a procedure, the surgical condition will be scored by one surgeon using a 5-point surgical rating scale. The rating scale is a 5-point ordinal scale ranging from 1 = poor condition to 5 = optimal surgical conditions. The surgeon will score the condition at 15 minute intervals.The values given on the surgical rating scale are averaged and the average value is used in the data analysis.

Time frame: Peroperative

ArmMeasureValue (MEAN)Dispersion
HypocapniaSurgical Rating Scale4.86 units on a scaleStandard Deviation 0.4
NormocapniaSurgical Rating Scale4.75 units on a scaleStandard Deviation 0.4
p-value: 0.59Mixed Models Analysis
Secondary

Hemodynamics

Hemodynamic conditions are studied during low arterial CO2 concentration and normal arterial CO2 concentration. The average of the measured mean arterial pressures at 15 minute intervals during anesthesia are presented

Time frame: peroperative

ArmMeasureValue (MEAN)Dispersion
HypocapniaHemodynamics85 millimeters of mercuryStandard Deviation 10
NormocapniaHemodynamics81 millimeters of mercuryStandard Deviation 9
Secondary

Nausea

The effect of low versus normal pCO2 concentrations on the incidence of postoperative nausea will be studied. The incidence is expressed as the percentage of people experiencing nausea per arm.

Time frame: from the end of surgery untill 2 hours postoperative

ArmMeasureValue (NUMBER)
HypocapniaNausea3.6 percentage of patients
NormocapniaNausea5.9 percentage of patients
Secondary

Pain Intensity on an 11-point Scale in the Postoperative Period

The effect of low versus normal pCO2 concentrations on postoperative pain will be studied. Painscores are obtained at 15 minutes intervals and are expressed as a number on a 10 point scale (numeric rating scale; 1 (low)-10(maximum)). The data is avaraged over time

Time frame: from the end of surgery untill 2 hours postoperative

ArmMeasureValue (MEAN)Dispersion
HypocapniaPain Intensity on an 11-point Scale in the Postoperative Period4.1 units on a scaleStandard Deviation 3.3
NormocapniaPain Intensity on an 11-point Scale in the Postoperative Period4.0 units on a scaleStandard Deviation 3.1
Secondary

Respiratory Function

The effect of low versus normal pCO2 concentrations on the postoperative respiratory function will be studied. Postoperative saturations are obtained at 15 minutes intervals. The data are averaged over time.

Time frame: from the end of surgery untill 2 hours postoperative

ArmMeasureValue (MEAN)Dispersion
HypocapniaRespiratory Function98.6 percentage of oxygen saturationStandard Deviation 2.1
NormocapniaRespiratory Function98.5 percentage of oxygen saturationStandard Deviation 2
Secondary

Sedation

The effect of low versus normal pCO2 concentrations on postoperative sedation will be studied using the using the validated Leiden Observer's Assessment of Alertness/Sedation (0 (awake) - 6 (unarousable)) scale at 15 min intervals. The data are averaged over time.

Time frame: from the end of surgery untill 2 hours postoperative

ArmMeasureValue (MEAN)Dispersion
HypocapniaSedation2.4 units on a scaleStandard Deviation 0.9
NormocapniaSedation2.3 units on a scaleStandard Deviation 0.8
Secondary

Vomiting

The effect of low versus normal pCO2 concentrations on the incidence of postoperative vomiting will be studied. The incidence of vomiting is expressed as a precentage of the patients per arm.

Time frame: from the end of surgery untill 2 hours postoperative

ArmMeasureValue (NUMBER)
HypocapniaVomiting0 percentage of patients
NormocapniaVomiting3.9 percentage of patients

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026