|Effect of Supplementing Oxygen with Positive end Expiratory Pressure During Elective Caesarean Section under Spinal Anaesthesia on Foetus.|
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|PMID: 21547172 Owner: NLM Status: PubMed-not-MEDLINE|
|BACKGROUND: It is known fact that pre-oxygenation with positive end-expiratory pressure (PEEP) improves the Partial pressure of oxygen (PO (2)). In this regard not many studies have been done in pregnant women to know its effect on foetus. In this randomised double blind controlled study, we analysed effect of pre-oxygenation with PEEP during caesarean section on foetal umbilical venous PO (2). PATIENTS #ENTITYSTARTX00026;
METHODS: 40 term pregnant women, ASA I or II, undergoing elective Caesarean section under spinal anaes-thesia were randomly divided into PEEP and Non-PEEP groups of 20 each. PEEP group received oxygen flow of 6 L/minute with PEEP of 5 cmH (2)O using a modified Mapleson A circuit with fixed unidirectional PEEP valve at the expiratory port during pre-oxygenation and Non PEEP group received same fresh gas flow of oxygen using same breathing circuit without PEEP. Maternal arterial blood samples were collected before applying PEEP and at the end of 5 minutes of facemask application for oxygen analysis. Immediately after baby was delivered umbilical venous samples were taken for blood gas analysis.
RESULTS: Both groups were comparable in terms of maternal baseline oxygen saturation (Spo (2)) and base line Po (2). After 5 minutes PO (2)was higher in PEEP Group than non PEEP group (491.65 + 49.96 vs. 452.08 + 77.61). Umbilical venous Po (2)in PEEP group was higher than non PEEP group (34.22 + 6.50 vs. 28.29 + 6.10 mm of Hg).
CONCLUSION: Application of PEEP during pre-oxygenation for spinal anaesthesia can increase foetal umbilical venous PO(2).
|Ramesh Prabhu; Jayaraj; U Kailasanath Shenoy|
|Type: Journal Article|
|Title: Journal of anaesthesiology, clinical pharmacology Volume: 26 ISSN: 2231-2730 ISO Abbreviation: J Anaesthesiol Clin Pharmacol Publication Date: 2010 Oct|
|Created Date: 2011-05-06 Completed Date: 2011-07-14 Revised Date: 2014-01-24|
Medline Journal Info:
|Nlm Unique ID: 9516972 Medline TA: J Anaesthesiol Clin Pharmacol Country: India|
|Languages: eng Pagination: 470-4 Citation Subset: -|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): J Anaesthesiol Clin Pharmacol
Journal ID (publisher-id): JOACP
Publisher: Medknow Publications & Media Pvt Ltd, India
Copyright: © Journal of Anaesthesiology Clinical Pharmacology
Print publication date: Season: Oct–Dec Year: 2010
Volume: 26 Issue: 4
First Page: 470 Last Page: 474
PubMed Id: 21547172
Publisher Id: JOACP-26-470
|Effect of Supplementing Oxygen with Positive end Expiratory Pressure During Elective Caesarean Section under Spinal Anaesthesia on Foetus|
|U Kailasanath Shenoyaff3|
|Associate Professor, Department of Anaesthesiology, Kasturba Medical College, Manipal, India
|Resident, Department of Anaesthesiology, Kasturba Medical College, Manipal, India
|Additional Professor, Department of Anaesthesiology, Kasturba Medical College, Manipal, India
|Correspondence: Correspondence: Dr. Ramesh Prabhu, email@example.com
It is common practice to supplement oxygen to parturient before caesarean section by either nasal prongs or face mask. The effect of the positive end expiratory pressure (PEEP) on improving partial pressure of oxygen (PO2) is well established. However, not many similar studies have been done in pregnant women in this regard and also to know its effect on foetus. In this randomised double blind controlled study, we analysed effect of the application of PEEP during pre-oxygenation on the maternal PO2and umbilical venous PO2in foetus.
The prospective randomised controlled was commenced after obtaining approval from hospital ethical committee. Written informed consent was taken from all the patients.
40 term pregnant women, ASA I or II, undergoing elective lower segment Caesarean section under spinal anaesthesia were randomly divided in to PEEP and Non-PEEP groups of 20 each.
Parturients with cardiopulmonary diseases, pre-eclampsia, anaemia, haemoglobinopathies, history of smoking, ante-partum haemorrhage, multiple gestations, antenatally diagnosed placental anomalies, hyper maturity of placenta, with foetal distress and any condition which likely to compromise foetal oxygenation were excluded from the study.
All patients kept 8 hours Pre-operative fasting. Observer (Resident Anesthesiologist) premedicated Parturient with tab ranitidine 150mg and tab. metoclopramide 10mg orally hr before surgery. Parturients were randomly divided into either of the two groups by drawing shuffled sealed lots and were shifted in left lateral position to the operating room and standard monitors were connected. Baseline vitals were recorded. Intravenous line was secured on non-dominant hand and all patients were preloaded with 15ml kg-1 body weight lactated Ringer's solution. An arterial line was secured in radial artery of non-dominant hand with 20 gauge cannula and maternal arterial blood sample was taken for baseline blood gas analysis. Spinal anaesthesia was performed in left lateral position with 2 ml of 0.5% bupivacaine (heavy) by observer 2 (Consultant Anesthesiologist). We aimed for a sensory block of T4 -T5 dermatome level. Immediately after giving the spinal anaesthesia patients were positioned supine with 15° lateral tilt of operating table. Hypotension (more than 20% decrease in mean arterial blood pressure from the baseline) was managed with boluses of ringer's lactate solution(crystalloid) followed by boluses of 6mg ephedrine as required and the intervention details were recorded.
After positioning supine, PEEP group received oxygen flow of 6 L/minute with 5 cmH2O PEEP using a modified Mapleson's A circuit with a fixed unidirectional PEEP valve (Armstrong medical™) (figure 1) at the expiratory port during pre-oxygenation and Non PEEP group received the same fresh gas flow of oxygen without PEEP using the same breathing circuit. Observer 2 applied facemask and maintained it tight sealing during the pre-oxygenation till baby delivery. All patients breathed oxygen via mask at normal tidal volume and rate during pre-oxygenation with closed mouth.
Another maternal arterial blood sample was collected at the end of 5 minutes of facemask application for Po2analysis.
Inability to maintain tight mask fit at any time, inadequate spinal anaesthesia and further administration of general anaesthesia were excluded from the study.
The timings of spinal anaesthesia, pre-oxygenation, uterine incision, baby delivery and intervals between these were noted using a stopwatch.
Immediately after delivery of the baby obstetrician triple clamped the umbilical cord with an extra cord clamp at 10 centimetres proximally towards the placental side. The umbilical cord was cut between the two distal clamps. Umbilical venous samples were taken for blood gas analysis between the two clamps by obstetrician.
Observer 3 (Resident Paediatrician) who was blinded regarding the pre-oxygenation sequence assessed the newborn's Apgar score at 1 and 5 minutes and recorded the birth weight.
After the delivery, the mothers in PEEP group were made to breathe 100% oxygen via the same circuit with out PEEP for 3 minutes and those in Non-PEEP group were made to breathe from the same circuit with 5 cm H2O PEEP for 3 minutes to assess the compliance of the mothers to simple mask holding and mask holding with application of PEEP. Compliance to mask holding and compliance to PEEP application were recorded separately
Maternal and umbilical cord blood samples were analysed using Roche omni C™ blood gas analyser immediately after sampling.
Independent sample t-test was used in analysing the demographic data, comparison of time intervals, maternal and umbilical blood gas analysis data, birth weight of newborn. Pearson Chi-square test was used in analysing the comparison of crystalloid bolus requirement. Fisher's Exact test was used in the comparison of requirement of ephedrine and atropine as well as analysing the maternal compliance to PEEP application and conventional mask holding. Mann Whitney U test was used in analysing the Apgar scores.
Data was expressed in mean mean ± standard deviation and median as necessary and p< 0.05 is considered significant. (Data was analysed using SPSS for Windows release 11.0.0. (19 Sep 2001).)
40 term pregnant women of ASA physical status I and II were analysed in the study. All parturients of both groups were comparable in terms of age, weight, height, body mass index, parity and gestational age. Table 1 shows analysis of spinal anaesthesia to baby delivery interval, uterine incision to baby delivery interval, start of pre-oxygenation to baby delivery interval. There was no significant difference between groups of these intervals.
There was no significant difference in requirement of crystalloid and ephedrine boluses for treating hypotension between the groups.
Both groups were comparable in terms of maternal baseline oxygen saturation (Spo2) and base line Po2. After 5 minutes Po2in PEEP Group was higher than non PEEP group (491.65±49.96 vs. 452.08±77.61) but it was statistically not significant as shown in table 2. The minimum and maximum values for maternal arterial blood oxygen tension at 5 minutes of pre-oxygenation in PEEP group were 358 and 593 mmHg respectively where as those for Non-PEEP group were 289 and 548 mmHg.
We analysed data regarding the need of reassurance for the mother while undergoing either of the techniques as shown in figure 3. It was found that there was no statistically significant difference between either techniques regarding patient compliance.
Umbilical venous oxygen saturation in PEEP group was 57.69±14.39% where as in non PEEP group it was 46.36±14.99 and umbilical venous oxygen tension in PEEP group was 34.22±6.50 mm of Hg where as in non PEEP group it was 28.29±6.10 mm of Hg. The differences between the groups were statistically significant as shown in table 3. (One umbilical blood gas result excluded because of the technical error during sample analysis).
Studies have established the fact that by increasing maternal PaO2, foetal PO2 can be increased as oxygen diffuses across the placenta by pressure gradient6, 7, 8, 9. Study by Ramanathan S et al regarding the optimum FIO2 for Caesarean section under epidural anaesthesia showed a linear increase in foetal oxygenation with the appraisal of maternal PaO27. Later, the existence of such an increase and its merits and demerits were questioned by many other studies10–11.
In our study, we evaluated whether the application of PEEP improves maternal and foetal PO2in comparison with a control of Non-PEEP group during spinal anaesthesia. We started supplementing 100% oxygen after established spinal anaesthesia and this may not exactly replicate a pre-oxygenation before general anaesthesia. This is because in our study, the spinal anaesthesia was aimed at T4 -T5 dermatomal level, which might interfere with the normal breathing12.
Shelley and Gutsche states that 6 min of oxygen inhalation is required for equilibration of foetal oxygen levels after the change in maternal values13. Myers et al studying Rhesus monkeys showed that maternal administration of oxygen increases foetal tissue PO2beginning within 60 seconds and equilibrating with 3 minutes14. Longo and Power constructed a systems model of placental O2transfer and suggest that foetal oxygen levels completely respond within 75 seconds to changes in umbilical oxygen supply15. Norris et al have shown that in the parturient both 3 min of oxygen breathing and the four-deep breath, 30-s technique are adequate for pre-oxygenation prior to rapid sequence induction of general endotracheal anaesthesia for Caesarean section16. Considering those factors we decided to take maternal blood samples after 5 minutes of pre-oxygenation for blood gas analysis. Maternal PaO2 in PEEP group after 5 minutes of pre-oxygenation was slightly more than Non-PEEP group (491.65±49.96 versus 452.08±77.6). Even though the values were not showing a significant difference statistically, a difference of 39 mmHg is seen between the groups which can be of clinical importance in a difficult intubation situation.
The umbilical venous PO2 in PEEP group was found to be significantly higher than Non-PEEP group (34.22±6.50 versus 28.29±6.10). This showed that pre-oxygenating with PEEP increases the umbilical venous PO2. There were no findings of foetal distress and all babies were having a normal Apgar score. The umbilical venous blood pH also was comparable between both groups. Question may arise as when there is no significant difference in the maternal PO2 how can there be a significant difference in the umbilical venous PO2? A probable explanation for this is as the mother is breathing 100% O2 there could have been formation of absorption atelectasis which was prevented by applying PEEP. So in our patients the elevated PaO2 at 5 minutes of oxygen may not have sustained in Non-PEEP group because of possible atelectasis formation17–19. But such an existence of atelectasis is not analysed directly in our study.
We consider that the compliance of the mother to the pre-oxygenation techniques will be a significant confounding factor for the efficacy of the techniques. We collected data regarding the need of reassurance for the mother for either of the techniques. An interchanging of the techniques of oxygen application was conducted immediately after the delivery. Our study showed that there was a clinically significant increase in the number of mothers needed reassurance with PEEP application when compared with Non-PEEP group. We consider that non- compliance can be a factor which needs attention in subjecting an already distressed mother to the PEEP application. In such a situation one has to weigh the risks and benefits of the PEEP, individualising to the situation.
In summary our study showed that application of PEEP during pre-oxygenation for spinal anaesthesia can increase maternal arterial PO2and foetal umbilical venous PO2 when compared to Non-PEEP Group and is tolerated by majority of the individuals studied.
Authors disclosure: Authors have no conflict of interest & financial consideration.
|1.||Herriger A,Frascarolo PH,Spahn D,Magnusson L. The effect of positive airway pressure during pre-oxygenation and induction of anaesthesia upon duration of non-hypoxic apnoeaAnaesthesiaYear: 200459243714984521|
|2.||Cressey DM,Berthoud Mc,Reilly CS. Effectiveness of continuous positive airway pressure to enhance pre-oxygenation in morbidly obese womenAnaesthesiaYear: 2001566708911437769|
|3.||Gander S,Franscarolo P,Suter M,Spahn DR,Magnusson L. Positive end-expiratory pressure during induction of general anaesthesia increases duration of nonhypoxic apnoea in morbidly obese patientsAnesth AnalgYear: 2005100580415673897|
|4.||Coussa m,Proietti S,Schnyder P,Franscarolo P,Suter M,Spahn DR,Magnusson L. Prevention of atelectasis during induction of anesthesia in morbidly obese patientsAnesth AnalgYear: 2004981491515105237|
|5.||Ferrandiere M,Hazouard E,Ayoub J,et al. Non-invasive ventilation corrects alveolar hypoventilation during spinal anesthesiaCan J AnaesthYear: 200653404816575042|
|6.||Baraka A. Correlation between maternal and foetal Po2 and Pco2 during Caesarean sectionBr J AnaesthYear: 19704243485431544|
|7.||Ramanathan S,Gandhi S,Arismendy J,Chalon J,Turndorf H. Oxygen transfer from mother to fetus during Cesarean section under epidural anesthesiaAnesth AnalgYear: 198261576817201255|
|8.||Backe SK,Lyons G. Oxygen and elective Caesarean sectionBr J AnaesthYear: 2002884511881882|
|9.||Edelstone DI,Peticca BB,Goldblum LJ. Effects of maternal oxygen administration on fetal oxygenation during reductions in umbilical blood flow in fetal lambsAm J Obstet GynecolYear: 1985152335184003479|
|10.||Khaw KS,Wang CC,Ngan Kee WD,Pang CP,Rogers MS. Effects of high inspired oxygen fraction during elective Caesarean section under spinal anaesthesia on maternal and fetal oxygenation and lipid peroxidationBr J AnaesthYear: 200288182311883375|
|11.||Khaw KS,Ngan Kee WD,Lee A,et al. Supplementary oxygen for elective Caesarean section under spinal anaesthesia: useful in prolonged uterine incision-to-delivery interval?Br J AnaesthYear: 20049245182215013959|
|12.||Kelly MC,Fitzpatrick KT,Hill DA. Respiratory effects of spinal anaesthesia for Caesarean sectionAnaesthesiaYear: 199651112029038445|
|13.||Shelly WC,Gutsche BB. James FM III,Wheleer AS,Philadelphia,Davis FAAnesthesia for febrile parturient, Obstetric Anesthesia: The complicated patientYear: 1982297316|
|14.||Myers RE,Stange L,Joelsson I,Huzell B,Wussow C. Effects upon the fetus of oxygen administration to the motherActa obstet gynecol scandYear: 19775619520317994|
|15.||Longo LD,Power GG. Placental oxygen transfer, A systems approachRev Perinat MedYear: 19761134|
|16.||Norris MC,Dewan DM. Preoxygenation for cesarean section: a comparison of two techniquesAnesthesiologyYear: 19856282794003814|
|17.||Dery R,Pelletier J,Jacques A,Clavet M,Houde J. Alveolar collapse induced by denitrogenationCan J AnaesthYear: 1965125313|
|18.||Reber A,Engberg GWegenius G,Hendenstierna G. Lung aeration: The effect of pre-oxygenation and hyper oxygenation during total intravenous anaesthesiaAnaesthesiaYear: 19965173378795314|
|19.||Magnusson L,Spahn DR. New concepts of atelectasis during general anaesthesiaBr J AnaesthYear: 200391617212821566|
Inter-group comparison of maternal oxygen saturation and arterial blood oxygen tensions
Keywords: Pre-oxygenation, Positive end-expiratory pressure, Caesarean section, Foetus.
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