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DONOHOE - SHAKEN BABY SYNDROME (SBS) AND NON-ACCIDENTAL INJURIES (NAI)

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A doctor in Australia who is speaking out and testifying for these

wrongly accused parents and caregivers!

Sheri

SHAKEN BABY SYNDROME (SBS) AND NON-ACCIDENTAL INJURIES (NAI)

DR MARK DONOHOE

This document is a de-identified extract from medical reports prepared in

1999 by Dr Mark Donohoe in selected and typical cases of alleged shaking and

injuries to infants. It's purpose is to provide a framework for

assessing assumptions and evidence required for determining that

particular injuries were caused by intentional and violent shaking.

It is accompanied by a more

general assessment of the " quality of evidence " in the

research so far published (to late 1998) in the peer-reviewed medical

literature, along with a listing of the references reviewed for both

SBS/NAI and Terson's

syndrome.

1 THE SHAKEN BABY SYNDROME

It is not possible to address the specifics of any particular case without

addressing the general medical and scientific literature regarding the

so-called shaken baby syndrome (SBS). I have performed

such a review of the medical literature in order to assess the quality of

evidence related to

the diagnosis of SBS, and include this as Appendix I, along with the

references reviewed. The question which needs to be answered is not,

could this be a case of shaken baby syndrome? , because this is clearly

one possibility. The questions which need to be answered would appear to

be:

1/ does this case represent anything other than SBS? ; and

the related question

2/ how certain are we that this was a case of SBS, as opposed to

anything else?

This report seeks to reach an objective answer to these questions in this

particular case.

1.1 HISTORICAL ISSUES AND EVIDENCE FOR SBS

For doctors dealing with potentially abused children, the error of assuming

abuse, even when none has occurred, is acceptable and (some would argue)

necessary. It is certainly preferable to the alternative of failing to

identify abuse which has occurred. In the past, the medical profession seems

to have failed to identify cases of abuse, resulting in tragic outcomes for

families and for the children not identified in particular.

In the last decade or so, a concerted effort has been made to address this

historical blind-spot, and a number of advocacy groups for the rights of the

child have emerged. Public educational campaigns have arisen, bringing the

risks of shaking to the attention of the public, and the medical profession,

particularly in hospital emergency settings, tends to scrutinise all cases

of childhood injury or unexplained illness for evidence of abuse. On the

whole, this has been a positive change, and may have resulted in

decreases in death

or injury of babies and children, although this has yet to be demonstrated.

As with all 'swings of a pendulum', however, there are associated

dangers of such increased surveillance for abuse. The most obvious risk is

that cases not associated with abuse will be incorrectly assumed to

be abuse, and that

the totality of evidence in cases will be ignored in favour of apparently

incriminating evidence. I say this because it is, even in

theory, impossible to attain perfection in the correct attribution of

cause of injury. In the past, actual abuse cases were missed as a

result. Now, cases

unrelated to abuse are occasionally incorrectly attributed to abuse. The

medical tests which are supportive of the diagnosis of non-accidental injury

(NAI) have been pushed by many advocates as being proof of NAI generally,

and SBS in particular. The diagnosis of NAI and SBS rests on a number of

factors, including medical and social history, family circumstances,

medical examination, a wide range of test results, and the results

of investigations

and interviews by experienced multi-disciplinary teams. The diagnosis of NAI

or SBS cannot ever rest upon the results of a few isolated investigations

alone, as has been the case in recent years.

There are two main reasons for pursuing suspected NAI vigorously, namely:

identifying and punishing any perpetrator, should the person be found;

and decreasing further risk to the abused child and other children in

the family. While the medical profession may well be acting in the

interests of the child by assuming NAI even when it has not

occurred, one must recognise

the potential for harm to the family and child where such

assumptions prove to

be incorrect. The decision on whether or not NAI has occurred, and who is

responsible for it if it has occurred, must be made by the legal process,

and such judgements must be dispassionate and based on evidence, rather

than assertion by those wishing to protect the child. While it is

self-evident

that the safety and rights of the child must be protected in every case, the

rights of the parents and carers cannot be ignored or forgotten in so doing.

There is a clear risk in assuming that abuse has occurred in cases where the

evidence is weak, and where alternative opinions have not been adequately

pursued and excluded. The cases which I have so far reviewed would never

have been investigated for potential abuse had it not been for the medical

findings, as there was no evidence of or suggestion of abuse. In such cases,

NAI has been assumed where other alternative explanations not only exist,

but are arguably more likely than NAI.

Finally, the tendency of the medical profession to ignore the possibility of

adverse reactions to vaccines, especially those containing thiomersal (a

mercury preservative), is important. In more than half of the cases I have

reviewed, there is an apparent temporal relationship between the injury and

prior vaccination with thiomersal-containing polyvalent vaccines or

multiple simultaneous vaccinations. The vaccine typically leads to pyrexia

and crying immediately following vaccination, and the infant is given

paracetamol (acetaminophen) at increasing doses for control of crying

and pyrexia in the

following days. In most of these cases, a broad spectrum antibiotic has also

been prescribed in the same period. It has been suggested that the

alternative explanation should be preferred, namely that the vaccination

itself caused no injury, but induced crying which lasted for days, leading

to frustration and eventual shaking by a parent or carer. Even if this is

accepted, it raises a most interesting issue of ultimate causation. Had the

vaccine(s) not been administered, the adverse reaction and crying would not

have occurred, and there would have been no risk or likelihood of shaking or

injury of any type. The acceptance of such crying and pyrexia as a " normal

and expected " consequence of polyvalent vaccinations in up to 20% of

infants does nothing to address the consequences of the crying and the

increased risk of injury to the child from such a common event. It

is disingenuous

to argue that " the disease would have been worse " than the

vaccination, because the disease may

or may not have occurred, and is a part of normal life of a child, whereas

vaccination is a procedure requiring informed consent. If one identifiable

risk of vaccination is that of shaking and injury following prolonged crying

(assuming that shaking did occur as a result of the vaccine-induced crying),

then this needs to be conveyed to parents of children being vaccinated as

part of the informed consent. If they are made aware of the potential for

prolonged crying and pyrexia, and are told of the risks associated with

shaking which may be a consequence of this crying, then the risk itself may

be reduced.

Thus, it is arguable that vaccination is an independent predictor (or risk

factor) for neurological injuries in infants, whether it is directly

causative or predisposes to other outcomes which are causative. A

recognition of the association (direct or indirect) may allow for action

and warnings which may decrease the likelihood of adverse outcomes.

1.2 AXIOMS AND ASSUMPTIONS REGARDING ALLEGATION OF SBS

The case for this infant being the victim of intentional shaking rests upon

certain axioms and assumptions, which may be reduced to the following:

1/ subdural haemorrhage (SDH) does not occur in a normal, healthy infant;

2/ combined with retinal haemorrhage (RH) is pathognomonic of

non-accidental injury (NAI);

3/ in the absence of identifiable external trauma, SDH and RH are only

caused by violent " acceleration/deceleration " actions caused by an

adult, otherwise known as 'shaken baby syndrome';

4/ SBS must be intentional, or at least they would appear intentional and

excessive to any dispassionate observer;

5/ the diagnosis of 'shaken baby syndrome' can be made with absolute

certainty on the basis of ophthalmological and radiological

assessment alone.

6/ the severity of shaking required to cause these findings would have been

obvious, and was unrelated to any shaking or corporal punishment admitted to

by family members. I shall address each of these statements separately, and

attempt to assess the evidence for and against each statement.

1.2.1 SPONTANEOUS SUBDURAL HAEMORRHAGE (SDH) DOES NOT OCCUR IN A NORMAL,

HEALTHY INFANT

Clearly, SDH should not occur in a 'normal healthy infant',

although there is no medical or scientific evidence to back this assertion

one way or the other. There is a logical difficulty, of course, in

that any such cases

which did occur in a 'normal healthy infant' would almost

certainly be attributed to NAI, whether or not there was other evidence

to support such an attribution. This is a part of a broader defect of

logic in NAI cases, that

all unexplained injuries can be assumed to be NAI, which has been allowed to

continue in an effort to protect the child. There is evidence that SDH does

occur in normal, healthy neonates as a result of birth trauma, and even in

cases of normal, uncomplicated vaginal delivery. There is clear evidence

that SDH can be caused by anatomical, infectious and biochemical

disorders which cause no obvious symptoms prior to the intracranial

bleeding. In such

circumstances, the infant appears 'normal and healthy'

(although probably not robustly healthy) despite the underlying,

predisposing pathology.

Such disorders, predisposing to SDH, include:

1 arteriovenous malformations (AVM) or shunts (AVS);

2 certain infections such as malaria, hepatitis, septicaemia;

3 intravascular coagulopathy due to bacterial endotoxin;

4 certain malignancies, such as leukaemia;

5 clotting disorders;

6 accidental or intentional poisoning;

7 liver disease, such as microvesicular steatosis, hepatitis, etc;

8 gastrointestinal disorders, causing malabsorption, affecting trace

elements, ascorbate or fat soluble nutrients (esp vitamins E and K);

9 metabolic disorders, such as Reye's syndrome, diabetes, disorders

of energy metabolism;

10 inherited disorders, such as enzyme defects or chromosomal defects;

11 vascular and connective tissue disorders.

This list is not intended to be exhaustive. It is also possible that more

than one predisposing factor existed, and that it was a combination of

factors which led to the intracranial haemorrhage. For example, a mild

factor XIII deficiency, when combined with malabsorption or Reye's

syndrome,

would be likely to result in a greater risk of intracranial bleeding

than would any one of these factors alone.

In an infant under six months, such disorders may be asymptomatic,

or may simply

result in a non-specific failure to thrive. In some of these diseases, the

first presentation is that of an intracranial bleed. It is only possible to

exclude these other causes by careful history taking, examination,

appropriate and extensive testing, including assessment of nutritional

status, enzyme levels, and assessing pathology of the liver, gut, kidneys,

muscle, brain and heart. It is my view, based on the cases I have reviewed,

that there is a tendency to assume that NAI has occurred in infants with SDH

and RH, and as a consequence of that assumption, there is a general failure

in the first instance to pursue other potential causes or contributions to

the injury as vigorously as would be expected.

Further, once the allegation of abuse has been made, and police or welfare

services have become involved, there is a general unwillingness to consider

any other plausible causes of the injury. In a sense, the parents or carer

are assumed to be guilty, and have no logical way of " proving "

their innocence. Investigations are continued, even if the infant dies,

but those investigations are usually directed at building a stronger

case for NAI

(such as bone scan, MRI, autopsy), rather than identifying alternative

causes or contributory factors.

1.2.2 SDH COMBINED WITH RETINAL HAEMORRHAGE (RH) IS PATHOGNOMONIC OF

" NON-ACCIDENTAL INJURY " (NAI);

This is frequently the claim made by medical experts involved in the

prosecution of SBS cases. Unless this relationship is proven, there is

reasonable doubt that anyone shook or otherwise injured this infant. The

term " pathognomonic " implies a two-way relationship between the

symptoms and signs on one hand, and the disease in question on the other

hand. Pathognomonic symptoms or signs not only allow recognition of

a disease, but

differentiate it from all other diseases or disorders. Technically, it

implies 100% specificity for the tests establishing the diagnosis.

The combination of SDH and RH strongly support a diagnosis of NAI, but in no

way constitute proof that NAI occurred. The value of the diagnosis of SDH

and RH is that their presence can markedly increase the confidence of

a diagnosis

of NAI, given other circumstances or findings which may indicate NAI. Even

if we assume that all non-accidental injuries involving shaking or blunt

trauma to the head of babies cause subdural haemorrhage and retinal

haemorrhage, it

does not follow that all cases of SDH and RH are caused by NAI.

One must know what other diseases or circumstances may cause SDH and RH.

Since the mechanism of RH is unknown (Riffenburgh 1991), it is important

that the specific hallmarks of NAI be delineated, as proposed recently

(Rohrbach 1997). Rohrbach (1997) has stated, " Intraretinal

haemorrhages alone are

typical, though not pathognomonic for the " battered-child syndrome " .

According to Rohrbach, the combination of the following provides increased

certainty of NAI, although there are clearly shortcomings in this single

case study:

1 retinal haemorrhage;

2 crater-like appearance of central retina;

3 haemorrhagic retinoschisis; and

4 intrascleral haemorrhages in the area of the circle of Zinn-Haller.

The ophthalmologists examining the infant needs to be questioned as to

whether the changes seen in the particular case match these proposed

criteria.

Conditions apart from NAI which may result in SDH and RH include: bleeding

disorders; meningitis; septicaemia; leukaemia; galactosaemia; hypertension;

and Henoch-Schonlein purpura. RH may also occur simply as a consequence of

the intracranial bleeding. A number of papers which deal with the mechanism

of the RH have suggested that the increasing intracranial pressure and

subarachnoid haemorrhage lead to retinal haemorrhages (i 1986), and

these may be accompanied by SDH.

In fact, this association is known as " Terson's syndrome " .

A number of papers (Giangiacomo 1985, Weingeist 1986, i 1986,ahn

1993, Poepel 1994) point out the similarities between Terson's

syndrome and the

retinopathy of shaken baby syndrome, with some suggesting that SBS should be

considered in the differential diagnosis of Terson 's syndrome. Thus,

there are other plausible and reasonable explanations for the combination

of SDH and RH in an infant. Any of the factors listed above as

potential causes of

SDH must be considered a plausible cause of the RH as well. The presence of

SDH and RH is insufficient to prove any particular cause. It is likely that

the majority of cases in which SDH and RH are found in infants under one year

of age are NAI, but this is a statistical association. In any given case,

these findings are only supportive of NAI. The case must stand or fall on

other factors which would lead one to suspect NAI.

1.2.3 IN THE ABSENCE OF EVIDENCE OF IDENTIFIABLE EXTERNAL TRAUMA, SDH AND RH

ARE ONLY CAUSED BY VIOLENT " ACCELERATION/DECELERATION "

ACTIONS CAUSED BY AN ADULT, KNOWN AS " SHAKEN BABY SYNDROME " ;

Most studies show a high proportion of NAIs are associated with other signs

of trauma or abuse, either in the damaged infant or in other family members.

In a recent British retrospective study (Jayawant 1998), about 60% showed

signs of other trauma (bruising, fractures, resolving old SDH, etc). Other

authors have suggested similar or higher percentages as showing signs of

trauma or abuse, especially in cases of severe cerebral damage and death

( 1990, Duhaime 1987, Lancon 1998).

As noted above, factors which may cause or contribute to SDH or SAH in an

infant are likely to cause RH as well. A recent study (Jayawant 1998) noted

an 80% association between SDH and RH, suggesting that RH is not an

independent risk predictor, but a marker of severity and extensiveness of

intracranial bleeding.

A number of authors (Duhaime 1987, Lancon 1998, Closset 1992) have suggested

that shaking without impact does not generate sufficient forces to cause the

types of injuries seen in SBS cases. Many others disagree, holding that

shearing forces tend to rupture the fragile veins across the dural space.

These other authors propose ways in which shaking with a rotatory component,

possibly at particular frequencies, or with rapid deceleration caused by

soft impact (eg pillow, etc), could cause such shearing.

In fact, if this view of rotation at particular frequencies is correct, it

is likely that the forces required to cause the damage observed may be less

important than had previously been thought.

There is no case definition for SBS, and this tends to cause problems in

deciding if a particular case is one of SBS. Many authors have taken the

view that any unexplained presentation of SDH and RH in an infant is

NAI until proven

otherwise. While useful as a medical " rule of thumb " , it

should be noted that this leads to a reversal of the burden of proof if

applied in a legal setting, and can result in the assumption of guilt

in blameless carers. If

all unexplained cases are defined as NAI or SBS, then the circular

definition results in carers having to prove their innocence, which is

logically impossible for this condition. The essential ingredient of

SBS would appear

to be strong evidence of shaking and NAI. The majority of studies, however,

assume that all unexplained cases of SDH and RH are SBS and NAI, and do not

determine the degree of confidence that the assumption is correct.

In addition, the actions said to be required to cause NAI have changed over

time from fore-aft shaking with impact, to severe and prolonged fore-aft

shaking without impact, to rotatory acceleration-deceleration without

impact, and more recently to rotatory acceleration-deceleration with soft

object impact. Without a clear case definition, and without a means

of proving whether an

unobserved carer performed the particular actions required, the attribution

of unexplained SDH and RH to SBS is neither provable nor disprovable. It is

not a question which can be scientifically decided with current knowledge

and techniques, and does not meet Popper 's test of a valid scientific

hypothesis (that an experiment can be defined which could disprove the

hypothesis, were it to be incorrect). The diagnosis rests on the

presence of sufficient

" other factors " which would raise suspicion of NAI, and the clinical,

ophthalmological and radiographic findings become supportive, rather than

diagnostic, in such circumstances.

1.2.4 SBS MUST BE INTENTIONAL, OR AT LEAST THEY WOULD APPEAR INTENTIONAL TO

ANY DISPASSIONATE OBSERVER;

This is, again, neither provable nor disprovable. Any concept of intention

is not a medical or scientific issue, as it can only be decided by the

person accused of shaking. As such, this becomes a matter for

determination through

the legal process. As the issue is one of degree (some degree of shaking and

head movement in infants being an aspect of normal play and day to day

life), the matter cannot be decided as it could for impact injuries,

suffocation or penetrating injuries (which are not part of a

continuum of normal life

activities). There are few data or cases in which the precise actions or

forces used to create the injuries have been determined or observed. The

lack of observational or experimental data make it impossible to determine

what an independent, dispassionate observer would perceive. It may be a

reasonable assumption that the rareness of the SBS-type injury

(estimated incidence in

Britain at less than one in 4,000 children per year - Jayawant 1998) would

imply excessive force. This may be a false assumption, however, if the

damage arises from a particular type of action, rather than simply being a

function of applied force. Rhythmic rotation of the baby at a

particular frequency,

for example, would be expected to lead to an amplification of applied force

and relative motion between brain and skull in the infant. Such shaking may

appear to be benign, yet cause significant damage to the dural vessels.

1.2.5 THAT THE DIAGNOSIS OF " SHAKEN BABY SYNDROME " CAN BE

MADE CONFIDENTLY ON THE BASIS OF CLINICAL AND X-RAY ASSESSMENT ALONE.

As noted above, typical clinical and radiological changes seen in SBS cannot

" make the diagnosis " , but can strongly support the diagnosis

made by other means. If the social and family circumstances are suggestive

of NAI, then the medical investigations and clinical findings can

increase the confidence

that a NAI has occurred, and can help define the likely process of the

NAI. The question arises as to how one goes about excluding a

diagnosis which has no

formal definition, and no unique defining characteristics.

A recent paper (Jayawant 1998) defines a number of characteristics of

supposed and " proven " NAI in children in a retrospective study, and the

findings of this would appear to suggest a set of criteria which, if

applied, may increase the precision of the diagnosis.

Nine factors suggesting NAI are identified in children who have suffered

SDH, namely:

Social and Family Issues

1. Sex of the child allegedly abused? (two thirds are male)

2. Sex of the alleged abuser? (four fifths are male)

3. Is there a past known history of abuse of this child or siblings by this

alleged abuser? (about one eighth have previously abused)

4. Is the explanation/history internally consistent? (over half of carers

change their stories two or three times)

5. Did the alleged perpetrator admit to shaking? (about half do, eventually)

Investigations and clinical findings

6. Haemoglobin at presentation less than 10 g/L (seen in half of NAI cases)

7. Skeletal survey (positive in 60% of NAI cases tested)

8. Evidence of some trauma or previous trauma (seen in about 60% of NAI)

9. Retinal haemorrhages (present in 80% of cases)

Of the nine proposed key factors in identification of NAI, the number found

in any particular case may be important in determining likelihood of

SBS/NAI.

1.2.6 THE SEVERITY OF SHAKING REQUIRED TO CAUSE THESE FINDINGS WOULD HAVE

BEEN OBVIOUS, AND WAS UNRELATED TO ANY SHAKING OR

CORPORAL PUNISHMENT ADMITTED TO BY FAMILY MEMBERS.

This can only be decided from an assessment of the social and family

circumstances, and a knowledge of the family's past history and even

around the time of the alleged injury. Evidence would be required that one

of those with access to the infant in the period during which the

injury is thought

to have occurred had previously shaken or abused either the baby or

another member of the family.

Additionally, the person would need to be proven to have the strength

necessary to shake the child in the manner thought to be required to induce

the injury. Without such evidence, and based solely upon the presence of

subdural haemorrhage and retinal haemorrhage, it would seem that the

attribution of the pathology to intentional abuse cannot be sustained.

Dr Mark Donohoe

20/8/01

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