Characteristics, course and outcomes of children admitted to a paediatric intensive care unit after cardiac arrest.
The true incidence of paediatric cardiac arrest is unknown, but out-of-hospital cardiac arrest (OHCA) events are estimated at 9 per 100 000 person years, whereas arrest within intensive care units is thought to occur 0.94 times per 100 admissions. [11-13] A large proportion (40-55%) of OHCAs in children occur in infants compared with other age categories. [12,14-16] In children, respiratory and cardiovascular failure are the major causes of cardiac arrest, but cardiac arrhythmias may not be as uncommon as was previously thought. 
The understanding of factors influencing, and the sequence of events leading to, cardiac arrest is thought to have contributed to improved survival.  Early recognition of patients at risk of arrest, timeous intervention and instituting effective cardiopulmonary resuscitation (CPR) that involves ventilation, chest compression and pharmacological agents, with ongoing monitoring and management following return of spontaneous circulation (ROSC), may all contribute to improved survival following cardiac arrest. [19,20]
Although the process of cardiac arrest and resuscitation is a continuum, it may be seen to consist of four phases: prearrest; no flow; low flow, and ROSC. [21,22] The prearrest phase may be associated with respiratory failure or shock states, which can result in asphyxia or ischaemia and so lead to inadequate delivery of substrate for cellular metabolism. This phase, if untreated, leads to established cardiac arrest, with the cessation of mechanical activity of the heart, absent pulses and a no-flow state. The low-flow phase ensues when CPR is instituted. The main goal of intervention at this stage is to optimise cerebral, coronary and other vital organ perfusion. Effective, uninterrupted chest compression at this stage is key to a successful outcome.  Abnormalities in oxygenation and ventilation are also common during the initial hours after paediatric cardiac arrest.  It therefore makes clinical sense to optimise oxygenation and haemodynamic stability [24,25] with ventilator support, fluids and inotropic support as required, to ensure improved survival of patients following cardiac arrest. 
The main objectives of this study were: to describe the characteristics, course and outcomes of patients admitted to the paediatric intensive care unit (PICU) following cardiac arrest; to compare the outcomes of patients following in-hospital cardiac arrest (IHCA) and OHCA, and to review factors associated with outcomes based on the Utstein-style reporting of cardiac arrest. 
Study setting and population
This retrospective study was conducted at the PICU of the Red Cross War Memorial Children's Hospital (RCWMCH) in Cape Town, South Africa (SA). This is a teaching hospital with 290 paediatric beds. The multidisciplinary PICU has 22 functional beds and accepts patients from birth to 13 years of age from general paediatric wards, the emergency and trauma department, surgical wards and operating theatres within the hospital, and also serves as a referral centre for patients from elsewhere in the Western Cape province.
Although there is no dedicated response team in the event of cardiac arrest or potential collapse within the hospital, an intercom system is used to alert medical staff to the event. Initial resuscitation is performed by ward personnel, with assistance from those who respond to the call. There is no clear protocolised guide for terminating CPR; this decision is taken by the resuscitation team when they think treatment is futile, which is usually after 20 - 30 minutes. In cases of OHCA, the patient may be resuscitated by bystanders or, if available, trained emergency medical personnel.
The study population consisted of all children <14 years of age who were admitted to the PICU between 01 January 2010 and 31 December 2011 following a documented cardiac arrest outside of the PICU, with CPR and ROSC. The patients were identified through review of the electronic PICU database.
As a general policy, the standard management of post-arrest syndrome and its complications was based on published recommendations, including targeting normal temperature or mild hypothermia, a blood glucose level of 8 - 10 mmol/L, ventilation support and early goal-directed haemodynamic stabilisation. [26,28] Lung-protective ventilation strategies were used to target normal oxygenation. 
Data were extracted from medical folders and entered into a case record form modified for IHCA or OHCA using the Utstein-style guidelines. [27,29] Information collected included: patient demographics; Paediatric Index of Mortality (PIM2) score on PICU admission;  cardiac arrest aetiology (according to primary diagnostic category ) and location (IHCA or OHCA); duration of CPR; advanced life-support medications used; initial cardiac rhythm; monitoring at the time of arrest; laboratory blood tests, and PICU management (including inotropic support and mechanical ventilation).
The primary outcome was PICU mortality. Secondary outcomes were: level of consciousness at PICU discharge according to the 'alert, voice, pain, unresponsive' (AVPU) scale;  hospital survival; length of stay in hospital and the PICU, and neurological outcome 3-6 months after PICU discharge, measured using the Paediatric Overall Performance Category (POPC) scale, as per standard practice at a follow-up clinic.  For the purposes of this study, prolonged CPR was defined as intervention continuing for >30 minutes, which is beyond the usual norm. For patients who had multiple arrests, data from the first arrest were used. Definitions of other terms used in this paper are presented in Table 1.
Approval for the study was obtained from the institutional Human Research Ethics committee (ref. no. 344/2012). The requirement for written informed consent was waived owing to the retrospective nature of the study.
Data were captured in Epi Info[TM] 18.104.22.168 software and exported to a spreadsheet. Statistica version 11 (Statsoft Inc., USA) was used to analyse the data. The Shapiro-Wilk test was used to test the distribution of continuous data. Numerical variables are presented as medians and interquartile ranges (IQRs) throughout, as appropriate for non-parametric data. The Mann-Whitney U test was used to compare continuous variables between survivors and non-survivors of cardiac arrest events. Pearson's [chi]-squared test (95% confidence interval) was used to test for associations of categorical variables. Kruskal-Wallis analysis of variance was used to determine the impact of CPR duration on POPC-scale outcome classifications. Factors significantly associated with PICU mortality on univariate analysis (p<0.05) were entered into a stepwise backward logistic regression analysis model to determine independent predictors of the outcome. A significance level of p<0.05 was used.
A total of 45 417 patients were admitted to the hospital over the period of study, of whom 2 501 (5.5%) required PICU admission. Of the PICU patients, 110 (4.4%) were admitted following cardiac arrest, representing a hospital incidence of 2.4 per 1 000 hospital admissions and 44.0 per 1 000 PICU admissions. Data were available for 103 of the 110 cardiac arrest patients and were subsequently included in the study (Fig. 1).
Characteristics of the included patients are presented in Table 2. The majority of participants (n=30; 29.1%) had primary respiratory disease underlying their arrest, most commonly associated with acute lower respiratory infections (n=21; 70.0%).
Twenty-nine cardiac arrests (28.2%) resulted from progressive deterioration in patients with a diagnosed medical condition; four (3.9%) events were expected, and in nine (8.7%) cases the underlying conditions prior to arrest were not documented. Of the 28 arrests during a procedure, 24 (85.7%) occurred during endotracheal intubation, two (7.1%) occurred intraoperatively, one (3.6%) during cardiac catheterisation and one (3.6%) during insertion of a central venous line. Of the 24 arrests that occurred during endotracheal intubation, 16 (66.7%) occurred in the emergency department, wards or other hospitals and eight (33.3%) occurred in theatre. Supervision by senior medical staff was documented for only two (12.5%) of 16 patients who arrested while undergoing intubation in the emergency department. The majority (80%) of patients who were in shock during intubation received inotropic support prior to arresting.
Location of arrest
IHCA occurred in 83 (80.6%) of the patients, whereas OHCA was documented in 20 (19.4%) cases (Table 3). 'Other' IHCA events included six (7.2%) cases that occurred during interhospital transfer in the ambulance.
Physiological and laboratory findings
Less than a fifth of the patients (n=19; 18.4%) had a documented cardiac rhythm recorded at arrest: four (21.1%) had pulseless electrical activity, asystole was recorded in ten (52.6%) cases and five patients (26.3%) had ventricular tachycardia or fibrillation. Temperature at arrest was recorded for 17 patients (16.5%), of whom 14 (82.4%) were hypothermic and two (11.8%) had hyperthermia; one patient (4.8%) in this group was normothermic.
The first blood chemistry results after the arrest and ROSC are presented in Table 4.
Management of arrest
The median duration of resuscitation (and associated IQR) was 10 (5-20) minutes. Prolonged CPR (>30 minutes) was performed on five patients (4.9%). Fig. 1 and Table 5 summarise peri-arrest management interventions. A third of the patients (n=34; 33.0%) did not receive any adrenaline during the resuscitation, whereas 44 (42.7%) received up to three doses of adrenaline and 24 (23.3%) received more than three doses. At least one defibrillation was performed in 13 (13.7%) of the 95 patients treated this way. One (1%) patient was cardioverted for supraventricular tachycardia following CPR.
The majority of patients (n=98; 95.1%) received ventilator support after ROSC. Only one patient received non-invasive continuous positive airway pressure, with the remainder all being intubated and ventilated mechanically. The median duration of mechanical ventilation (and associated IQR) was 2 (0 - 5) days. Close to three-quarters of the patients (n=74; 71.8%) received inotropes during their PICU admission.
Post-arrest organ complications
Circulatory failure was the most common complication following cardiac arrest, with 71 patients (68.9%) clinically shocked following the arrest. Neurological complications were recorded in 25 (24.3%) cases, with seizures (n=18) representing 72.0%, persistent loss of consciousness (n=4) 16.0% and focal signs (n=3) 12.0%. A total of 25 patients (24.3%) developed acute kidney injury according to the so-called 'paediatric risk, injury, failure, loss, end stage renal disease' (pRIFLE) criteria. Some patients had more than one complication.
The median lengths of stay in the PICU and hospital (with associated IQRs) were 3 (1 - 8) and 27 (9 - 52) days, respectively. More than half of the patients (n=63; 61.2%) survived to PICU discharge - 52 (82.5%) following IHCA and 11 (17.5%) following OHCA (p=0.7) (Table 6). Of the 40 PICU deaths, 20 (50%) occurred within 24 hours of arrest. The standardised mortality rate (actual/mean predicted mortality using the PIM2 score) was 0.7. Factors associated with PICU mortality on univariate analysis included: underlying neurological conditions; duration of resuscitation; PIM2 score; post-arrest pH, chloride, creatinine and lactate; receipt of inotropes in the PICU, and neurological sequelae post arrest (Tables 5 and 6). On multiple regression analysis, none of these variables were found to be independently associated with PICU mortality.
Of the 63 patients who were discharged from the PICU, four died in the wards. Two of these deaths were documented as being unrelated to the cardiac arrest, whereas no association was documented for the remaining two deaths.
Assessment of level of consciousness on PICU discharge was conducted using the AVPU criteria: 54 of the 63 PICU survivors (85.7%) were discharged from the PICU alert, one (1.6%) was responsive to voice, four (6.3%) to pain; one (1.6%) was unresponsive, and the level of consciousness was not documented in three cases. Of the 59 patients who were discharged from hospital, 51 (86.4%) were assessed neurologically and developmentally 3 - 6 months post discharge. According to the POPC scale, 32 (62.7%) were classified as normal and seven (13.7%) displayed mild disability. Moderate and severe disability was recorded in six patients (11.8%) in each of the respective groups. None were in a persistent vegetative state. Duration of resuscitation had no effect on POPC outcome (p=0.7).
This retrospective study of PICU admissions following cardiac arrest in a single SA tertiary centre showed a prevalence of 2.4 per 1 000 hospital admissions over the period under review. This figure is likely to be an underestimate of the true prevalence of cardiac arrest in the hospital, as we were unable to collect data on patients who did not survive to ROSC and PICU admission. Further research is warranted to determine overall prevalence and outcomes of cardiac arrest. Arrest episodes occurred predominantly in infants younger than 1 year, similar to other reports. [35,36]
Respiratory, cardiac and gastrointestinal disorders were the most common primary diagnostic conditions related to cardiac arrest. We were unable to classify the precipitating cause of arrest into hypoxia/asphyxia or circulatory shock, [22,37] owing to the retrospective nature of this study and inadequate reporting. Our data showed that underlying respiratory and gastrointestinal diseases were more likely to be of recent onset (mainly acute lower respiratory tract infections and acute diarrhoeal disease), while cardiac disease was generally related to chronic comorbid conditions (congenital heart disease). Although not confirmed on the basis of our data, acute respiratory tract infections and other respiration-related causes were pathophysiologically most likely associated with hypoxia, while gastrointestinal diseases such as acute diarrhoeal diseases most likely precipitated circulatory failure or hypovolaemic shock. [38,39]
Two previous studies have evaluated IHCA: one in the form of a prospective study conducted in Brazil (a middle-income country with comparable characteristics to SA),  and the other being a retrospective study from Finland (a high-income country).  Although limited to IHCA, both these studies collected similar data using Utstein-style reporting. In both studies, the model of care and personnel managing patients with cardiac arrest were similar to our setting. We found a 57.3% survival-to-hospital-discharge rate. This is similar to the findings of the Finnish study,  but differs considerably from the rate (25.3%) reported in the Brazilian study.  For both the Finnish and Brazilian studies, the most common precipitating cause of arrest was cardiac in nature (71% and 61%, respectively), while in our study respiratory and cardiac conditions accounted for 29.1% and 21.4% of arrests, respectively. Although cardiac arrhythmias, ventricular tachycardia and fibrillation were documented in 4.8% (n=5) of our cases, we were unable to ascertain whether these were the primary underlying causes of cardiac arrest in these patients. Notably, initial electrocardiographic monitoring was extremely poor in our study, potentially introducing bias into our results, and these findings therefore need to be confirmed in prospective studies.
Our results showed that a clinically relevant proportion (23.3%) of cardiac arrest episodes occurred during endotracheal intubation procedures, mostly emergency intubations in the emergency department and hospital wards. Considering that most of these patients were likely to have been in peri-arrest status at the time of intubation, consequently with a high predicted risk of cardiac arrest, it is concerning that the majority of these endotracheal intubation procedures were not overseen by senior staff. It is therefore strongly recommended that emergency endotracheal intubation be considered a high-risk procedure, and that senior staff should be present to supervise whenever possible.
CPR is the mainstay of treatment for cardiac arrest. Effective CPR, with adequate depth of chest compression and rate, alternating with ventilation and oxygen, has significantly improved the outcome of paediatric cardiac arrest.  There is, however, insufficient evidence to recommend when to terminate CPR, although it has previously been shown that a short duration of CPR is the best prognostic indicator of survival in children.  However, in a study that included >3 000 children, Matos et al.  suggested that more patients may survive following prolonged CPR than previously thought. There does, however, remain the concern that prolonged CPR may lead to poor neurological outcome in survivors.  Five of the patients in our study (5%) had prolonged CPR, showing that in our setting, providers occasionally continued beyond the conventional period for terminating CPR, although this was not the norm. The reasons for prolonged resuscitation were not indicated in the patient hospital records. Although there was an association between duration of CPR and PICU mortality on univariate analysis, no association was found between duration of resuscitation and neurological outcome using the POPC scale. Furthermore, on multiple regression analysis, duration of resuscitation was no longer identified as a predictive factor for PICU mortality. Considering that poor neurological outcomes were recorded in only a small number of surviving patients in our study, further large-sample prospective studies are warranted to confirm our findings. As also seen in another study,  we found that shock was the most prevalent complication following an arrest, with acute kidney impairment and neurological impairment present in equal proportions.
A large proportion of the patients in our study who had successful CPR with ROSC survived to hospital discharge with reasonable neurological outcomes. Our observed hospital mortality rate of 42.7% (n=44) was comparable to the 43.2% reported by Suominen et al.  and the standardised mortality rate of 0.7 in our cohort indicates better-than-predicted PICU survival based on the PIM2 score at admission. The nature of this study did not allow for estimation of change in neurological status from pre- to post-arrest status, and this requires further investigation. Approximately three-quarters (n=39; 76.5%) of the patients who survived to hospital discharge and were available for follow-up had good neurological outcomes, with scores indicating normal function or only mild disability. Only six survivors (11.8%) had severe disability. These findings are almost identical to those of a large cohort study, which reported that good neurological outcome according to the POPC scale was documented in 76.7% of patients who survived to discharge. 
Our findings were limited by the retrospective study design, with inherent problems of selection bias, inadequate documentation and data capture resulting in potential missing data and risk of bias. The lack of a control group admitted to the PICU without prior cardiac arrest or a control group who did not survive their arrest further limits the interpretation of results. We captured data only of patients who arrived at the RCWMCH and were admitted to the PICU following successful resuscitation and ROSC. Population-based studies are necessary to determine the incidence and overall outcomes of cardiac arrests in the region.
Although we attempted, as far as possible, to report results according to the Utstein style, as recommended by paediatric studies such as that by Suominem et al.,  we were limited by the retrospective nature of the study and consequently poorly documented arrest circumstances. In some cases, monitoring equipment was not available at the time of the arrest and therefore some observations (e.g. arrest rhythm) were not documented and could not be fully reported on.
Notwithstanding the limitations, this study gives insight into paediatric cardiac arrest outcomes in SA, shown to be in line with those reported for a well-resourced country.  Results of our study could be used as a baseline or comparator for further studies and practice improvement initiatives, ultimately to inform policy and implement targeted, optimised management of paediatric cardiac arrest.
An essential starting point for future research is the establishment of appropriate, uniform and comprehensive documentation processes for cardiac arrest episodes, particularly for IHCA. Development of a cardiac arrest event registry, with feedback provided to medical and nursing personnel, may help to identify those at greater risk of cardiorespiratory arrest, sensitise staff to the issues related to arrest episodes in children, and improve documentation of these events.
Patients in the wards who could potentially be at risk of cardiac arrest should be flagged as high risk, and ideally nursed in high-dependency units with appropriate monitoring, staffing and equipment in order to elicit an appropriate response in the case of a deteriorating clinical condition with the potential for cardiac arrest.
In this retrospective study we found the incidence of cardiac arrest with successful resuscitation and ROSC preceding PICU admission to be 2.4 per 1 000 hospital admissions, with the majority occurring in children younger than 1 year. Acute respiratory failure and circulatory failure from gastrointestinal and cardiac conditions were the most common underlying causes of cardiac arrest. Children undergoing emergency endotracheal intubation constituted a notable proportion of this patient cohort. Mortality was lower than predicted in children admitted to the PICU following cardiac arrest, and the majority of survivors had normal neurological function on hospital discharge.
Acknowledgements. We thank all medical staf who contributed to the care of patients with cardiac arrest, administrative staf for making medical records available, and the Neurodevelopmental Clinic at RCWMCH, for their role in follow-up neurological testing and documentation.
Author contributions. JA was the student investigator for this study, supervised by SS, BM and AA. All investigators contributed to protocol development, data collection, analysis and interpretation, and contributed to preparing the draf of the manuscript.
Conflicts of interest. None.
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J Appiah, (1,2,3) MB ChB, MWACP, MPhil, Cert Crit Care (Paed); S Salie, (1,2) MB ChB, DCH, FCPaed, Cert Crit Care (Paed); A Argent, (1,2) MB ChB, MMed(Paed), MD(Paed), DCH (SA), FCPaed (SA); B Morrow, (2) PhD, BSc (Physiotherapy)
(1) Paediatric Intensive Care Unit, Red Cross War Memorial Children's Hospital, Cape Town, South Africa
(2) Department of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa
(3) Paediatric Intensive Care Unit, Department of Child Health, Komfo Anokye Teaching Hospital, Kumasi, Ghana
Corresponding author: J Appiah (firstname.lastname@example.org)
Accepted 15 October 2018.
S Afr J Crit Care 2018;34(2):58-64. DOI:10.7196/SAJCC.201.v34i2.355
Table 1. Definitions of terms used Term Definition Cardiac arrest Cessation of functional mechanical activity of the heart, with absent central pulses, unresponsiveness and apnoea Apnoea Cessation of breathing for >20 seconds Primary diagnosis The main condition treated or the most clinically severe or life-threatening condition that was deemed likely to have led to cardiac arrest Bradycardia Heart rate <80 beats per minute in the newborn to 2 years of age, or <60 beats per minute in children over 2 years of age Tachycardia Heart rate >160 beats per minute in the newborn to 2 years of age or more than twice normal for age Hyperthermia Documented axillary temperature >38.5 [degrees]C Hypothermia Documented axillary temperature <35.5 [degrees]C Shock A combination of any of the following: abnormal mental status; weak, thready pulses; prolonged capillary refill time and cold extremities; low blood pressure Acute kidney injury Acute decline in renal function measured by decreases in urine output and serum creatinine clearance post arrest episode, with specific pRIFLE scoring criteria to categorise the injury pRIFLE = paediatric risk, injury, failure, loss, end-stage renal disease. Table 2. Characteristics of the study population post cardiac arrest (N=103) Characteristics n (%) Male 60 (58.3) Age (months), median (IQR) 7.2 (2.5 - 21.6) Age (months) <1 12 (11.6) 1 - 12 52 (50.4) 12 - 36 22 (21.4) 36 - 72 10 (9.7) >72 7 (6.8) Weight (kg), median (IQR) 5.8 (3.7 - 10.0) PIM2 score, median (IQR) 0.54 (0.28 - 0.85) Primary diagnosis Neurological 9 (8.7) Tumour 3 (33.3) Hydrocephalus 1 (11.1) Meningitis 1 (11.1) Subdural haemorrhage 1 (11.1) Cerebral abscess 1 (11.1) Encephalitis 1 (11.1) Tuberculous meningitis 1 (11.1) Respiratory 30 (29.1) Acute lower respiratory tract infection 21 (70.0) Tuberculosis 1 (3.3) Foreign-body aspiration 2 (6.7) Aspiration 4 (13.3) Tension pneumothorax 1 (3.3) Pulmonary haemorrhage 1 (3.3) Cardiovascular 22 (21.4) Congenital heart disease 16 (72.2) Dilated cardiomyopathy and myocarditis 6 (27.3) Gastrointestinal 22 (21.4) Acute diarrhoeal disease 14 (63.6) Necrotising enterocolitis 3 (8.7) Intestinal perforation 2 (9.1) Bowel obstruction 1 (4.5) Gastric haemorrhage 1 (4.5) Protein energy malnutrition 1 (4.5) Trauma 4 (3.9) Abdominal 1 (25.0) Non-accidental injury 1 (25.0) Pedestrian motor vehicle accident 1 (25.0) Burns 1 (25.0) Other 16 (15.5) Drowning 5 (31.3) Sepsis 5 (31.3) Haematologic/oncologic 3 (18.8) Poisoning/drug overdose 2 (12.5) Disseminated tuberculosis 1 (6.3) IQR = interquartile range. Table 3. Locations of arrest event Arrest location n (%) Out of hospital 20 (19.4) At home 10 (50.0) Public place 10 (50.0) In hospital 83 (80.6) Emergency unit 18 (21.7) Wards 41 (49.4) Operating theatre 8 (9.6) Other 16 (19.3) Table 4. First blood biochemistry results following return of spontaneous circulation (N=103) Parameter Median (IQR) Blood glucose (mmol/L) 6.3 (4.3 - 13.5) pH 7.16 (6.99 - 7.30) Sodium (mmol/L) 138.0 (134.0 - 142.0) Potassium (mmol/L) 4.1 (3.6 - 5.1) Chloride (mmol/L) 106.0 (101.0 - 110.0) Ionised calcium (mmol/L) 1.26 (1.12 - 1.60) Creatinine ([micro]mol/L) 60.0 (36.5 - 88.0) Lactate (mmol/L) 5.4 (2.4 - 11.6) IQR = interquartile range. Table 5. Peri- and post-arrest management, monitoring and complications in survivors v. non-survivors PICU deaths Parameter (N=40), n (%) Peri-arrest management Duration of resuscitation (min) 17.5 (10 - 30) Number of adrenaline doses 0 12 (30.0) 1 7 (17.5) 2 7 (17.5) 3 5 (12.5) 4 3 (7.5) 5 2 (5.0) 6 4 (10) Number of defibrillation events (N=95) 0 35 (94.5) 1 1 (2.7) 2 0 (0.0) 3 0 (0.0) 6 1 (2.7) Peri-arrest monitoring ECG (N=19) Pulseless electrical activity 2 (40) Asystole 2 (40) Ventricular tachycardia/fibrillation 1 (20) Respiratory rate (N=42) Arrest/apnoea 12 (100) Tachypnoea 0 Blood pressure (N=43) Unrecordable 7 (36.8) Hypotensive 12 (63.2) Temperature (N=17) Hypothermic 7 (77.8) Normothermic 0 Hyperthermic 2 (22.2) Post-arrest management Inotropic support 34 (85) Invasive mechanical ventilation 40 (100) Post-arrest blood biochemistry (N=103) (*) pH 7.07 (6.88 - 7.20) Sodium (mmol/L) 139.0 (134.0 - 146.0) Chloride (mmol/L) 109.0 (103.0. -118.0) Magnesium (mmol/L) 1.1 (1.0 - 1.5) Calcium (mmol/L) 1.3 (1.1 - 1.5) Urea (mmol/L) 5.7 (3.2 - 7.3) Creatinine ([micro]mol/L) 79.0 (45.0 - 118.5) Lactate (mmol/L) 11.5 (5.2 - 15.7) Post-arrest complications Neurological 15 (37.5) Acute kidney injury 13 (32.5) Shock 32 (80.0) PICU survivors Parameter (N=63), n (%) Peri-arrest management Duration of resuscitation (min) 10 (5 - 15) Number of adrenaline doses 0 22 (34.9) 1 14 (22.2) 2 5 (7.9) 3 6 (9.5) 4 3 (4.8) 5 3 (4.8) 6 9 (14.3) Number of defibrillation events (N=95) 0 47 (81.0) 1 2 (3.4) 2 1 (1.7) 3 1 (1.7) 6 7 (12.1) Peri-arrest monitoring ECG (N=19) Pulseless electrical activity 2 (14.3) Asystole 8 (57.1) Ventricular tachycardia/fibrillation 4 (26.7) Respiratory rate (N=42) Arrest/apnoea 26 (86.7) Tachypnoea 4 (13.3) Blood pressure (N=43) Unrecordable 7 (29.2) Hypotensive 17 (70.8) Temperature (N=17) Hypothermic 7 (87.5) Normothermic 1 (12.5) Hyperthermic 0 Post-arrest management Inotropic support 40 (63.5) Invasive mechanical ventilation 57 (90.5) Post-arrest blood biochemistry (N=103) (*) pH 7.22 (7.09 - 7.36) Sodium (mmol/L) 137.0 (133.0 - 140.0) Chloride (mmol/L) 104.0 (101.0 - 129.0) Magnesium (mmol/L) 1.1 (0.9 - 1.3) Calcium (mmol/L) 1.2 (1.1 - 2.0) Urea (mmol/L) 5.5 (3.8 - 7.3) Creatinine ([micro]mol/L) 54.0 (34.0 - 72.0) Lactate (mmol/L) 3.2 (1.4 - 6.8) Post-arrest complications Neurological 10 (15.9) Acute kidney injury 12 (19.0) Shock 39 (61.9) p-value Parameter Peri-arrest management 0.006 Duration of resuscitation (min) Number of adrenaline doses 0.6 0 0.7 1 0.2 2 0.6 3 0.9 4 0.7 5 0.7 6 Number of defibrillation events (N=95) 0.2 0 0.7 1 0.8 2 0.8 3 0.2 6 Peri-arrest monitoring ECG (N=19) 0.96 Pulseless electrical activity 0.3 Asystole 0.7 Ventricular tachycardia/fibrillation Respiratory rate (N=42) 0.5 Arrest/apnoea 0.3 Tachypnoea Blood pressure (N=43) 0.5 Unrecordable 0.7 Hypotensive Temperature (N=17) 0.4 Hypothermic 0.8 Normothermic 0.3 Hyperthermic Post-arrest management 0.03 Inotropic support 0.1 Invasive mechanical ventilation Post-arrest blood biochemistry (N=103) (*) 0.001 pH 0.08 Sodium (mmol/L) 0.03 Chloride (mmol/L) 0.71 Magnesium (mmol/L) 0.64 Calcium (mmol/L) 0.89 Urea (mmol/L) 0.01 Creatinine ([micro]mol/L) <0.0001 Lactate (mmol/L) Post-arrest complications 0.02 Neurological 0.2 Acute kidney injury 0.09 Shock PICU = paediatric intensive care unit; ECG = electrocardiogram. Table 6. Demographic data and cardiac arrest aetiology of survivors v. non-survivors PICU deaths PICU survivors Variable (N=40), n (%) (N=63), n (%) Age (months), median (IQR) 9.0 (2.4 - 26.6) 6.6 (2.7 - 16.9) Weight (kg), median (IQR) 6.4 (4.1 - 12.0) 5.5 (3.3 - 9.5) Male 26 (65.0) 34 (54.8) PIM2 score, median (IQR) 0.83 (0.52 - 0.97) 0.41 (0.23 - 0.68) Underlying condition category Neurological 8 (20.0) 1 (1.6) Respiratory 10 (25.0) 18 (28.6) Cardiovascular 5 (12.5) 17 (27.0) Gastrointestinal 10 (25.0) 12 (19.0) Trauma 3 (7.5) 1 (1.6) Location of arrest OHCA 9 (22.5) 11 (17.5) IHCA 31 (77.5) 52 (82.5) Variable p-value Age (months), median (IQR) 0.38 Weight (kg), median (IQR) 0.21 Male 0.3 PIM2 score, median (IQR) <0.0001 Underlying condition category Neurological 0.002 Respiratory 0.4 Cardiovascular 0.1 Gastrointestinal 0.3 Trauma 0.3 Location of arrest OHCA IHCA 0.7 PICU = paediatric intensive care unit; IQR = interquartile range; PIM = Paediatric Index of Mortality; OHCA = out-of-hospital cardiac arrest; IHCA= in-hospital cardiac arrest.
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|Author:||Appiah, J.; Salie, S.; Argent, A.; Morrow, B.|
|Publication:||Southern African Journal of Critical Care|
|Date:||Nov 1, 2018|
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