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England and Wales High Court (Queen's Bench Division) Decisions |
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You are here: BAILII >> Databases >> England and Wales High Court (Queen's Bench Division) Decisions >> Anderson v North West Strategic Health Authority [2015] EWHC 3563 (QB) (08 December 2015) URL: http://www.bailii.org/ew/cases/EWHC/QB/2015/3563.html Cite as: [2015] EWHC 3563 (QB) |
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QUEEN'S BENCH DIVISION
CARLISLE DISTRICT REGISTRY
Strand, London, WC2A 2LL |
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B e f o r e :
____________________
JAMIE-LEE ANDERSON |
Claimant |
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- and - |
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NORTH WEST STRATEGIC HEALTH AUTHORITY |
Defendant |
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Mr Watson QC (instructed by Ward Hadaway) for the Defendant
Hearing dates: 18th to 25th November 2015
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Crown Copyright ©
The Hon Mr Justice Turner:
INTRODUCTION
BACKGROUND
i) the fact that the pregnancy had lasted 32 weeks;ii) the ruptured membranes;
iii) loss of vaginal blood; and
iv) variable accelerations[1] in the CTG readings.
He asked for a vaginal examination to be carried out and queried the possible use of oxytocin to induce labour. He considered the risk of the need for a caesarean section. Whether this was explained to Andrea at the time is an issue between the parties but it is not one which needs to be resolved for the purposes of this judgment. In any event, she was thereafter transferred to the labour ward.
THE RUPTURED MEMBRANES
BLEEDING
CARDIOTOCOGRAPHY
FIGO
"1.4. Certain patterns of electronically monitored FHR recordings are strongly associated with specific changes in fetal condition. However, not infrequently uncertainty exists in respect to interpretation. Unnecessary operative interventions might be the result of incorrect interpretation and overestimation of the diagnostic potential of electronic FHR monitoring. Therefore it cannot be emphasized enough that understanding and interpretation of a FHR record is not an easy matter and that formal training in the underlying physiology and the practise of FHR monitoring is indispensable for all those supposed to make decisions on FHR records. Furthermore it needs to be stressed that whereas certain FHR patterns are sensitive indicators of fetal hypoxia, the specificity is low. It is rarely possible to quantitate hypoxia on the basis of FHR records alone and information derived from FHR records only represents one piece of information which always has to be interpreted in the context of the clinical situation."
"Baseline fetal heart rate is the mean level of the fetal heart rate when this is stable, accelerations and decelerations being absent. It is determined over a time period of 5 or 10 min and expressed in beats/min (bpm).
Variability. …in clinical practice variability means long term variability. .. Long term variability is characterized by the frequency and the amplitude of the oscillations. Although the frequency may be important, it is difficult to assess correctly. Therefore variability is usually only quantitated by description of the amplitude of the oscillations around the baseline heart rate.
Accelerations. Transient increase in heart rate of 15 beats/min or more and lasting 15 s or more.
Decelerations. Transient episodes of slowing of fetal heart rate below the baseline level of more than 15 beats/min and lasting 10 s or more."
Definition of intrapartum fetal cardiotocogram
Normal pattern
Baseline heart rate between 110 and 150 beats/min.
Amplitude of heart rate variability between 5 and 25 beats/min.
Suspicious pattern
Baseline heart rate between 170 and 150 beats/min or between 110 and 100 beats/min.
Amplitude of variability between 5 and 10 beats/min for more than 40 min.
Increased variability above 25 beats/min.
Variable decelerations.
Pathological pattern
Baseline heart rate below 100 or above 170 beats/min.
Persistence of heart rate variability of less than 5 beats/min for more than 40 min.
Severe variable decelerations or severe repetitive early decelerations.
Prolonged decelerations.
Late decelerations: the most ominous trace is a steady baseline without baseline variability and with small decelerations after each contraction.
BOYLAN
"If conservative measures do not succeed in correcting the fetal heart rate abnormality, then delivery or scalp pH and blood gas measurement[2] should be undertaken, the course of action determined by the severity of the abnormality and the likely proximity of delivery."
"There is good evidence…that abnormal patterns in the preterm fetus are correlated, to a greater extent than term fetuses, with abnormal outcome."
GIBB AND ARULKUMARAN
"The most critical feature, however, is the evolution of the trace with time. A change in the baseline rate and change in the baseline variability are the key signs of developing hypoxia and acidosis…
Much time is wasted in discussion over whether decelerations are early, late or variable and whether they can be pigeon-holed into "good", "bad" and "possibly good". Such discussion is fruitless. It is not each contraction itself that is critical but it is the evolution of the trace with time. The baseline rate between contractions, baseline variability and presence or absence of accelerations is critical."
THE CRUCIAL PERIOD
THE MANAGEMENT PLAN
THE CTG TRACES FROM 11.26
THE CLINICAL PICTURE
i) the suspected placental abruption;ii) the ruptured membranes;
iii) the premature onset of labour;
iv) earlier decelerations which can be found within CTG traces commencing at 4.55 and 6.10 respectively; and
v) the CTG trace pattern after 11.26/7.
i) there had been no record of fresh vaginal bleeding over a period of about 36 hours immediately prior to labour;ii) the liquor produced during labour remained clear of blood;
iii) the risk that a significant abruption would occur did not increase as the labour progressed. It is arguable that it, in fact, decreased.
THE CTG TRACES
i) Although FIGO undoubtedly provided a useful guide to the classification and interpretation of CTG patterns, it did not purport to have a monopoly of wisdom on the appropriate parameters of categorisation;ii) Where interpretation is dependant on the duration of any given deceleration, care must be taken not to adhere too slavishly to a mechanistic stopwatch approach. A line must be drawn somewhere but this does not, for example, justify the clinician treating a deceleration lasting a second or two longer than another as automatically representing a step change in risk terms. Drawing such a line is an inevitable consequence of applying a digital scale to assess an analogue risk.
iii) Even with the aid of engineering and mathematical analysis, the categorisation of any individual trace can be controversial. For example, the measurement of deceleration must be made from the baseline level and not from such transient level as may have been reached immediately before the deceleration. Accordingly, for the clinician, there is inevitably an element of judgment by eye leaving some scope for legitimately differing views.
iv) The judgements of clinicians are formed in the context of busy obstetric units without the luxury which has been afforded to this court of CTG engineering analysis and hours of time within which to analyse the traces.
v) Simply because any given trace may fall into an "abnormal" category does not of itself require an intervention by the clinician. The pattern of traces is important and the assessment of the overall picture involves an exercise in clinical judgment that is incapable of being reduced to a readily defined algorithm.
vi) Such guidance as the literature provides puts considerable emphasis on the categorisation of CTG patterns but is understandably more reticent concerning the proper clinical response. Doubtless, this is at least in part because the CTG traces must be seen in the context of all of the information available to the clinician and not in isolation.
THE BALANCING ACT
APPLYING THE BOLAM TEST
i) Dr Thomas and Mr MacKenzie are both highly distinguished experts in their field as was amply demonstrated by their impressive CVs.ii) Despite relatively mildly articulated suggestions made by each side that the expert instructed by the other had lost objectivity or had otherwise fallen short in discharging his duty to the court, I formed the strong view that each was doing his objective best to assist me to reach the right conclusion.
i) In his report, Dr Thomas conceded that "There may be those who would contend that the CTG between 11.30 and 12.35 hours was suspicious rather than pathological." In giving evidence he further conceded that an obstetrician who had formed that view could not be said thereby to have reached a conclusion outside the range of opinion which could be held by a reasonable body of obstetricians.ii) In justifying his view that, despite such potential choice of categorisation, the case for an emergency caesarean was clear cut, he relied upon the additional factors of the suspected placental abruption, the ruptured membranes and the premature onset of labour as being decisive. However, as I have found, the additional risk caused by the breach the membranes was modest. The risk posed by the threat of abruption of the placenta was not insignificant but had not increased as the labour had progressed. The additional vulnerability of the preterm fetus was a relevant factor but one the assessment of which was very much a matter of clinical judgment. Dr Thomas certainly convinced me that a reasonable body of clinicians would have expedited a caesarean section against this background but he failed to persuade me that a conservative approach fell beyond the pale of Bolam reasonableness. The CTG patterns had undoubtedly deteriorated but Dr Dufour had noted this and discussed the way forward with Mr Brown in full knowledge of the complicating factors identified by Dr Thomas. Bearing in mind the caveats I have identified in approaching the categorisation and interpretation of CTG patterns, I reject the contention that the clinicians' conservative approach was wrong.
iii) I may well (and probably would) have reached a different conclusion if the CTG traces had recorded a change in the baseline rate and change in the baseline variability of the fetal heartbeat. These are the key signs of developing hypoxia and acidosis. However, it is to be noted that Dr Thomas, again with scrupulous fairness, endorsed in cross examination the Gibb proposition which advocates the critical importance of the evolution of the trace over time over debates about "whether decelerations are early, late or variable and whether they can be pigeon-holed into "good", "bad" and "possibly good". I stress that I am not suggesting that it is only where the CTG pattern reveals a change in the baseline rate and change in the baseline variability of the fetal heartbeat that urgent action may be mandated. I am merely using this hypothetical scenario as an example of circumstances in which, in contrast to the present case, a claimant may be able to surmount the challenge of establishing a breach of duty.
CONCLUSION
Note 1 He later explained that this was an error and that he intended to record “decelerations” rather than “accelerations”. I accept his evidence on this. [Back] Note 2 In the present case, it is agreed between the parties that taking a fetal blood sample was not an option which fell to be considered by the clinicians. [Back] Note 3 Although this publication post dates the events with which this court is concerned, it is not suggested that the views of the authors fell outside the scope of reasonable medical opinion in 1989. [Back] Note 4 As it happens, the suspicion of a partial abruption was found after delivery to have been unfounded but this revelation is not material to the consideration of what account should have been taken of the risk at the time the relevant clinical judgements were being made. [Back]