- Research article
- Open Access
- Open Peer Review
Acute posthypoxic myoclonus after cardiopulmonary resuscitation
- Aline Bouwes†1, 2Email author,
- Daniël van Poppelen†1,
- Johannes HTM Koelman3,
- Michael A Kuiper1, 4,
- Durk F Zandstra5,
- Henry C Weinstein2, 6,
- Selma C Tromp7,
- Eveline GJ Zandbergen8,
- Marina AJ Tijssen3, 9 and
- Janneke Horn1
© Bouwes et al.; licensee BioMed Central Ltd. 2012
- Received: 23 January 2012
- Accepted: 20 July 2012
- Published: 1 August 2012
Acute posthypoxic myoclonus (PHM) can occur in patients admitted after cardiopulmonary resuscitation (CPR) and is considered to have a poor prognosis. The origin can be cortical and/or subcortical and this might be an important determinant for treatment options and prognosis. The aim of the study was to investigate whether acute PHM originates from cortical or subcortical structures, using somatosensory evoked potential (SEP) and electroencephalogram (EEG).
Patients with acute PHM (focal myoclonus or status myoclonus) within 72 hours after CPR were retrospectively selected from a multicenter cohort study. All patients were treated with hypothermia. Criteria for cortical origin of the myoclonus were: giant SEP potentials; or epileptic activity, status epilepticus, or generalized periodic discharges on the EEG (no back-averaging was used). Good outcome was defined as good recovery or moderate disability after 6 months.
Acute PHM was reported in 79/391 patients (20%). SEPs were available in 51/79 patients and in 27 of them (53%) N20 potentials were present. Giant potentials were seen in 3 patients. EEGs were available in 36/79 patients with 23/36 (64%) patients fulfilling criteria for a cortical origin. Nine patients (12%) had a good outcome. A broad variety of drugs was used for treatment.
The results of this study show that acute PHM originates from subcortical, as well as cortical structures. Outcome of patients admitted after CPR who develop acute PHM in this cohort was better than previously reported in literature. The broad variety of drugs used for treatment shows the existing uncertainty about optimal treatment.
- Evoked potentials
Many patients remain comatose after successful cardiopulmonary resuscitation (CPR) due to brain damage caused by hypoxemia. Acute posthypoxic myoclonus (PHM) occurs in about 19-37% of these patients, typically within the first 24 hours after CPR, but knowledge about this illness is limited [1, 2]. Acute PHM can be divided into status myoclonus and (multi)focal myoclonus. In daily practice different terms are used for status myoclonus, e.g. generalized myoclonus, myoclonus status, or myoclonic status epilepticus [1, 3, 4]. Wijdicks et al. defined status myoclonus as spontaneous or sound-sensitive, repetitive, irregular brief jerks in both face and limb present during most of the first day after CPR . Specific EEG criteria were not mentioned. Focal myoclonus, such as platysmal myoclonus has also been reported in patients after CPR . Most studies concerning acute PHM were performed before treatment with hypothermia after CPR was implemented. Nowadays, acute PHM is often suppressed during the first day after admission by the administration of sedative drugs or neuromuscular blocking agents during hypothermia treatment. Stimulus sensitive myoclonus often interferes with nursing of these patients, is deterrent to relatives, and is difficult to treat. No evidence based guidelines for treatment exist [5–7]. Lance-Adams syndrome, chronic PHM, also occurs in patients after CPR, but usually arises in the post-intensive care unit period and it is mainly seen after hypoxia as primary cause of CPR [5, 8].
Based on clinical and electrophysiological features, one can discriminate between a cortical and subcortical origin of myoclonus. Clinically, cortically generated myoclonus is mostly focal or multifocal and mainly affects parts of the body with a large cortical representation, such as hand and face. Subcortical myoclonus, especially reticular myoclonus, is generalized, predominantly affecting axial and proximal limbs. Both types of myoclonus can be stimulus sensitive [6, 9–11]. Neurophysiologic investigations such as somatosensory evoked potential (SEP), electroencephalogram (EEG), electromyography (EMG), and EEG-EMG with back-averaging enable localization of the origin of myoclonus. Giant potentials on SEP recordings and epileptiform discharges or sharp/slow waves on the EEG suggest a cortical origin of the myoclonus [9, 12, 13]. In case of a subcortical origin of myoclonus, SEP is normal and there are no consistent abnormalities seen on the EEG [9, 13].
The pathophysiology of acute PHM is poorly understood [4, 5, 11]. Literature suggests that acute PHM originates from subcortical and/or cortical structures [5, 11]. A histological study in 15 patients with status myoclonus after CPR and 11 patients without myoclonus showed significantly more neuronal loss in all cortical laminae in patients with myoclonus, the extent of anoxic-ischemic damage in the hippocampus and cerebellum was similar in both patient groups .
For optimal treatment in patients with acute PHM, discrimination between cortical and subcortical origin of myoclonus would be helpful. Cortical myoclonus is primarily treated with levetiracetam or piracetam; subcortical myoclonus is usually treated with clonazepam [5–7, 14].
The aim of this study was to investigate the origin of acute PHM in patients after CPR by retrospectively analyzing SEP and EEG recordings.
Data were collected from the database of the prospective multicenter cohort study PROgnosis after PostAnoxic Coma II (PROPAC II study) . In the PROPAC II study 391 adult patients admitted after CPR were included between December 2007 and August 2009. All patients were treated with hypothermia. The research protocol and consent procedures of the PROPAC II study were approved by the medical ethics committees of the Academic Medical Center (NL19644.018.07) and all collaborating hospitals: Medical Center Leeuwarden, Onze Lieve Vrouwe Gasthuis, St. Antonius Hospital, Rijnstate Hospital, Medical Center Alkmaar (METC Noord-Holland), Kennemer Gasthuis (METC Noord-Holland), Spaarne Hospital (METC Noord-Holland), Reinier de Graaf Groep (METC Zuidwest Holland), and Sint Lucas Andreas Hospital. Informed consent was obtained from a legal representative shortly after the patient’s hospital admission. When the patient regained consciousness and was able to judge the situation properly, informed consent was also obtained from the patient.
For the present study, patients reported to have focal myoclonus or status myoclonus at 24–48 and/or 48–72 hours after CPR were considered to have acute PHM. Data from those patients were retrieved from the database. Myoclonus was scored on the case record form with no further differentiation of the severity and clinical characteristics; there was no score option for multifocal myoclonus. Patients who were scored to have both focal myoclonus and status myoclonus were considered to have status myoclonus. The following variables were used: gender, age, presenting cardiac rhythm, time to return of spontaneous circulation, medical history of epilepsy, use of sedative drugs or neuromuscular blocking agents during SEP.
Neurologic outcome was assessed with the Glasgow Outcome Scale (GOS) after six months . Good outcome was defined as GOS 4–5 (good recovery or moderate disability). At the time of data collection for this study, survivors were contacted by phone and asked if any form of myoclonus persisted.
Neurologic examination, including the motor score was performed 48 and 72 hours after CPR. In the PROPAC II study, cortical N20 responses of median nerve SEP were recorded with standard procedures during office hours in patients who remained comatose after regaining normal body temperature . For this study, SEP recordings were retrieved and assessed by JK. The SEP was documented as absent (bilaterally absent cortical N20 responses after left and right median nerve stimulation, with present cervical potential), present (cortical N20 response present on at least one side) or undeterminable (technically insufficient recording). If the N20 was present, the amplitudes of the P27/N35 potentials (after right sided stimulation) were scored as < 2 μV, 2–5 μV or > 5 μV. Left-right differences were scored. Giant potentials were defined as a P27/N35 potential > 5 μV. Absent SEPs were not further analyzed.
An EEG was not a standard examination for the PROPAC II study and therefore subject to physicians’ decision. Available EEG recordings were retrieved and evaluated by JH, all EEGs were recorded during normothermia. Presence of epileptic activity, status epilepticus, generalized periodic discharges, burst suppression, isoelectric/low voltage activity (< 20 μV), and background reactivity were scored.
Neurophysiologic criteria for cortical origin of the myoclonus were giant SEP potentials or epileptic activity, status epilepticus, or generalized periodic discharges on the EEG.
Medication administered for myoclonus or epileptic seizures was reported 48 and 72 hours after CPR and categorized as: sodium valproate, clonazepam, other benzodiazepines, phenytoin, levetiracetam, and propofol. The clinical effect of the administered drugs was not evaluated.
Patient characteristics were summarized using descriptive statistics. Variables were expressed as mean and standard deviation, or when not normally distributed, as medians and inter-quartile ranges.
Total number of patients, n
Age, y, mean (SD)
Male, n (%)
Initial rhythm, n (%)
Primary cause of CPR, n (%)
Time from collapse to BLS, min, median, (IQR)
Time to ROSC, min, median (IQR)
Medical history of epilepsy, n (%)
GOS after 6 months, n (%)
2 Vegetative state
3 Severe disability
4 Moderate disability
5 Good recovery
Acute posthypoxic myoclonus
Focal myoclonus, n
Status myoclonus, n
Present 24–48 h
Present 48–72 h
Present 24–48 h and 48–72 h
Characteristics of the performed somatosensory evoked potentials
Total number of performed SEPs
< 2 μV
> 5 μV (giant potential)
Characteristics of the performed electroencephalograms
Total number of performed EEGs
Generalized periodic discharges
Low voltage activity/isoelectric
Unable to assess
The criteria for a cortical origin of the myoclonus were fulfilled in 24/64 (38%) patients in whom SEP and/or EEG was performed.
Treatment of myoclonus
48 hours after CPR, n = 52
72 hours after CPR, n = 30
The results of this study show that acute PHM originates from subcortical, as well as cortical structures; in 38% of the patients, in whom neurophysiologic investigations were performed, strong evidence towards a cortical origin of the myoclonus was found. The limited clinical information on the signs of myoclonus due to the retrospective character of the study limits further conclusions. Our data also suggest that the outcome in patients with myoclonus after CPR, irrespective of their origin, is not invariably correlated with poor outcome as previously described in literature.
To determine the origin of myoclonus, EEG and SEP recordings were used in this study. Only a very small number of patients had a giant SEP potential. A giant SEP potential is compatible with hyperexcitability of the sensorimotor cortex and proves the cortical origin of myoclonus. These giant SEPs are especially found in patients with progressive myoclonic epilepsy. However, absence of a giant SEP potential does not rule out a cortical origin of the myoclonus . A reason for the low number of giant potentials of SEPs could be the flattening effect of different antiepileptic drugs, such as clonazepam, levetiracetam and sodium valproate on the amplitude of the giant SEP response [18–20]. Many patients in our study were treated with these types of drugs during SEP registration, which probably has led to an underestimation of a cortical origin.
Various EEG patterns in acute PHM patients are described in the literature; epileptic activity or sharp/slow waves on the EEG may suggest cortical origin, but does not proof it [9, 12, 13]. In 64% of the EEGs in our study, a cortical origin was suggested, as epileptic activity, status epilepticus, or generalized periodic discharges were seen . Furthermore, bursts of generalized spikes and polyspikes or a burst suppression pattern are often found on EEG, which is thought to be consistent with severe neuronal injury . Previous studies described a burst suppression pattern in 50-84% of patients with status myoclonus [1, 3, 4]. In our study, only 2/32 patients with status myoclonus had a burst suppression pattern. A possible explanation might be that the EEGs in our study were performed at different intervals after admission, which was previously studied by Thömke et al.. He showed that specific EEG-patterns in comatose patients with generalized myoclonus after CPR are often transient and change over time .
Rossetti et al. showed in a prospective cohort study of patients admitted after cardiac arrest and treated with hypothermia that 3/56 patients without EEG background reactivity survived until hospital discharge. None of these patients had a good outcome after 3–6 months . On the contrary with these findings, none of the 3 patients with EEG recordings and good outcome in our study showed background reactivity.
A study limitation was that the performance of an EEG was subject to physicians’ decision. In The Netherlands, SEPs are usually performed before EEGs are requested and in case of bilaterally absent cortical N20 responses, the majority of the physicians will withdraw supportive ICU treatment, so no further investigations are performed . This could have led to selection bias of patients in whom EEG was performed and it is possible that our results underestimate some of the EEG patterns in this type of patients.
In general, the outcome in our acute PHM population was better than expected based on previous publications. Several cohort studies before and after the introduction of therapeutic hypothermia after CPR reported survival rates of 0-11% for patients with acute posthypoxic myoclonus or myoclonic status epilepticus, with poor outcome for all survivors [1, 3, 4, 23–27]. Two studies from the 1980s of Celesia et al. and Levy et al. have reported independent functioning rates similar to our study, in 1/13 (8%) and 2/21 (10%) patients respectively [28, 29]. Recently, two studies in patients with myoclonus after cardiac arrest and treatment with hypothermia showed a good outcome in 3-10% [21, 30]. A likely explanation for the difference in mortality between the studies is the definition used for acute PHM and status myoclonus. The original definition of status myoclonus by Wijdicks et al. included revelation within 24 hours. Nowadays, acute PHM might be suppressed during hypothermia treatment due to administration of sedative drugs. Another possible explanation might be the limited number of patients with myoclonus in the studies.
Acute PHM is difficult to treat and knowledge about the origin in the brain could probably lead to better treatment and identification of patients with a more favourable outcome. In our study, various drugs were used for the treatment of acute PHM. This reflects the uncertainty about the best treatment for this syndrome [5, 14]. In general, cortical myoclonus is primarily treated with levetiracetam or piracetam; subcortical myoclonus is usually treated with clonazepam [5–7, 14]. Treatment with phenytoin, sodium valproate, phenobarbital or various benzodiazepines is often ineffective [1, 3, 25]. Propofol causes enhancement of gamma-amino butyric acid and has been successfully used as treatment of acute PHM [25, 31].
A study limitation is the retrospective method used to select patients from the PROPAC II study, which was designed to establish the validity of diagnostic methods to predict poor outcome in patients treated with mild hypothermia after CPR. The fact that not in all patients neurophysiologic tests were performed is also a limitation and might limit robust conclusions from this study. A study primarily investigating acute PHM should ideally contain video recording of the myoclonus in each patient, evaluation by blinded assessors and strict evaluation of the effect of standardized medication used. Furthermore, it should combine EEG and SEP recordings with EEG-EMG with back-averaging, as this last method can prove a cortical origin . Future research with the above mentioned standardized observation techniques, more neurophysiologic tests, and randomized treatment groups are necessary to evaluate the effect of different treatment strategies.
Despite the limitations mentioned above we think that acute PHM originates from subcortical, as well as cortical structures and that the outcome of patients admitted after CPR who develop acute PHM might be better than previously reported. The broad variety of drugs used for treatment shows the existing uncertainty about optimal treatment.
The PROPAC II study was financially supported by a research grant, received by Dr. Horn, from the Dutch Heart Foundation (2007B039). The funder had no role in study design; the collection, analysis, and interpretation of data; the writing of the article and the decision to submit it for publication. We would like to thank Jan Binnekade (statistical analyses); and Annelou van der Veen (Academic Medical Center, Amsterdam), Lenny Kranstauber-van Wijngaarden (Onze Lieve Vrouwe Gasthuis, Amsterdam), Matty Koopmans (Medical Center Leeuwarden, Leeuwarden), Leo Koster (Kennemer Gasthuis, Haarlem), Daan Kamphuis (Reinier de Graaf Groep, Delft), and Björn van Geel (Medical Center Alkmaar, Alkmaar) (study support).
- Wijdicks EF, Parisi JE, Sharbrough FW: Prognostic value of myoclonus status in comatose survivors of cardiac arrest. Ann Neurol. 1994, 35: 239-243. 10.1002/ana.410350219.View ArticlePubMedGoogle Scholar
- Snyder BD, Hauser WA, Loewenson RB, Leppik IE, Ramirez-Lassepas M, Gumnit RJ: Neurologic prognosis after cardiopulmonary arrest: III. Seizure activity. Neurology. 1980, 30: 1292-1297. 10.1212/WNL.30.12.1292.View ArticlePubMedGoogle Scholar
- Thömke F, Marx JJ, Sauer O, Hundsberger T, Hagele S, Wiechelt J, Weilemann SL: Observations on comatose survivors of cardiopulmonary resuscitation with generalized myoclonus. BMC Neurol. 2005, 5: 14-10.1186/1471-2377-5-14.View ArticlePubMedPubMed CentralGoogle Scholar
- Young GB, Gilbert JJ, Zochodne DW: The significance of myoclonic status epilepticus in postanoxic coma. Neurology. 1990, 40: 1843-1848. 10.1212/WNL.40.12.1843.View ArticlePubMedGoogle Scholar
- Venkatesan A, Frucht S: Movement disorders after resuscitation from cardiac arrest. Neurol Clin. 2006, 24: 123-132. 10.1016/j.ncl.2005.11.001.View ArticlePubMedGoogle Scholar
- Obeso JA: Therapy of myoclonus. Clin Neurosci. 1995, 3: 253-257.PubMedGoogle Scholar
- Dijk JM, Tijssen MA: Management of patients with myoclonus: available therapies and the need for an evidence-based approach. Lancet Neurol. 2010, 9: 1028-1036. 10.1016/S1474-4422(10)70193-9.View ArticlePubMedGoogle Scholar
- Lance JW, Adams RD: The syndrome of intention or action myoclonus as a sequel to hypoxic encephalopathy. Brain. 1963, 86: 111-136. 10.1093/brain/86.1.111.View ArticlePubMedGoogle Scholar
- Caviness JN, Brown P: Myoclonus: current concepts and recent advances. Lancet Neurol. 2004, 3: 598-607. 10.1016/S1474-4422(04)00880-4.View ArticlePubMedGoogle Scholar
- Chang VC, Frucht SJ: Myoclonus. Curr Treat Options Neurol. 2008, 10: 222-229. 10.1007/s11940-008-0024-y.View ArticlePubMedGoogle Scholar
- Hallett M: Physiology of human posthypoxic myoclonus. Mov Disord. 2000, 15 (Suppl 1): 8-13.View ArticlePubMedGoogle Scholar
- Shibasaki H, Yamashita Y, Neshige R, Tobimatsu S, Fukui R: Pathogenesis of giant somatosensory evoked potentials in progressive myoclonic epilepsy. Brain. 1985, 108 (Pt 1): 225-240.View ArticlePubMedGoogle Scholar
- Cassim F, Houdayer E: Neurophysiology of myoclonus. Neurophysiol Clin. 2006, 36: 281-291. 10.1016/j.neucli.2006.10.001.View ArticlePubMedGoogle Scholar
- Frucht S, Fahn S: The clinical spectrum of posthypoxic myoclonus. Mov Disord. 2000, 15 (Suppl 1): 2-7.View ArticlePubMedGoogle Scholar
- Bouwes A, Binnekade JM, Kuiper MA, Bosch FH, Zandstra DF, Toornvliet AC, Biemond HS, Kors BM, Koelman JH, Verbeek MM, Weinstein HC, Hijdra A, Horn J: Prognosis of coma after therapeutic hypothermia: a prospective cohort study. Ann Neurol. 2012, 71: 206-212. 10.1002/ana.22632.View ArticlePubMedGoogle Scholar
- Jennett B, Bond M: Assessment of outcome after severe brain damage. Lancet. 1975, 1: 480-484.View ArticlePubMedGoogle Scholar
- Zandbergen EG, Hijdra A, de Haan RJ, van Dijk JG, Ongerboer de Visser BW, Spaans F, Tavy DL, Koelman JH: Interobserver variation in the interpretation of SSEPs in anoxic-ischaemic coma. Clin Neurophysiol. 2006, 117: 1529-1535. 10.1016/j.clinph.2006.03.018.View ArticlePubMedGoogle Scholar
- Okuma Y, Shimo Y, Shimura H, Hatori K, Hattori T, Tanaka S, Kondo T, Mizuno Y: Familial cortical tremor with epilepsy: an under-recognized familial tremor. Clin Neurol Neurosurg. 1998, 100: 75-78. 10.1016/S0303-8467(98)00003-1.View ArticlePubMedGoogle Scholar
- Striano P, Manganelli F, Boccella P, Perretti A, Striano S: Levetiracetam in patients with cortical myoclonus: a clinical and electrophysiological study. Mov Disord. 2005, 20: 1610-1614. 10.1002/mds.20530.View ArticlePubMedGoogle Scholar
- Ikeda A, Kakigi R, Funai N, Neshige R, Kuroda Y, Shibasaki H: Cortical tremor: a variant of cortical reflex myoclonus. Neurology. 1990, 40: 1561-1565. 10.1212/WNL.40.10.1561.View ArticlePubMedGoogle Scholar
- Rossetti AO, Oddo M, Logroscino G, Kaplan PW: Prognostication after cardiac arrest and hypothermia: a prospective study. Ann Neurol. 2010, 67: 301-307.PubMedGoogle Scholar
- Bouwes A, Kuiper MA, Hijdra A, Horn J: Induced hypothermia and determination of neurological outcome after CPR in ICUs in the Netherlands: results of a survey. Resuscitation. 2010, 81: 393-397. 10.1016/j.resuscitation.2009.12.032.View ArticlePubMedGoogle Scholar
- Hui AC, Cheng C, Lam A, Mok V, Joynt GM: Prognosis following postanoxic myoclonus status epilepticus. Eur Neurol. 2005, 54: 10-13. 10.1159/000086755.View ArticlePubMedGoogle Scholar
- Zandbergen EG, Hijdra A, Koelman JH, Hart AA, Vos PE, Verbeek MM, de Haan RJ, (PROPAC Study Group): Prediction of poor outcome within the first 3 days of postanoxic coma. Neurology. 2006, 66: 62-68. 10.1212/01.wnl.0000191308.22233.88.View ArticlePubMedGoogle Scholar
- Thömke F, Weilemann SL: Poor prognosis despite successful treatment of postanoxic generalized myoclonus. Neurology. 2010, 74: 1392-1394. 10.1212/WNL.0b013e3181dad5b9.View ArticlePubMedGoogle Scholar
- Fugate JE, Wijdicks EF, Mandrekar J, Claassen DO, Manno EM, White RD, Bell MR, Rabinstein AA: Predictors of neurologic outcome in hypothermia after cardiac arrest. Ann Neurol. 2010, 68: 907-914. 10.1002/ana.22133.View ArticlePubMedGoogle Scholar
- Samaniego EA, Mlynash M, Caulfield AF, Eyngorn I, Wijman CA: Sedation confounds outcome prediction in cardiac arrest survivors treated with hypothermia. Neurocrit Care. 2011, 15: 113-119. 10.1007/s12028-010-9412-8.View ArticlePubMedPubMed CentralGoogle Scholar
- Levy DE, Caronna JJ, Singer BH, Lapinski RH, Frydman H, Plum F: Predicting outcome from hypoxic-ischemic coma. JAMA. 1985, 253: 1420-1426. 10.1001/jama.1985.03350340072020.View ArticlePubMedGoogle Scholar
- Celesia GG, Grigg MM, Ross E: Generalized status myoclonicus in acute anoxic and toxic-metabolic encephalopathies. Arch Neurol. 1988, 45: 781-784. 10.1001/archneur.1988.00520310099023.View ArticlePubMedGoogle Scholar
- Bisschops LL, van Alfen N, Bons S, van der Hoeven JG, Hoedemaekers CW: Predictors of poor neurologic outcome in patients after cardiac arrest treated with hypothermia: A retrospective study. Resuscitation. 2011, 82: 696-701. 10.1016/j.resuscitation.2011.02.020.View ArticlePubMedGoogle Scholar
- Wijdicks EF: Propofol in myoclonus status epilepticus in comatose patients following cardiac resuscitation. J Neurol Neurosurg Psychiatry. 2002, 73: 94-95. 10.1136/jnnp.73.1.94.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2377/12/63/prepub
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