Lin et al. published a meta-analysis on high-flow nasal cannula therapy (HFNC) in 2121 children with bronchiolitis younger than 24 months1. Six randomised controlled trials (RCTs) compared HFNC with standard oxygen therapy (SOT) and three with nasal continuous positive airway pressure (nCPAP). There were no significant differences in primary outcomes between the groups: length of hospital stay (LOS), length of oxygen supplementation, and transfer to the paediatric intensive care unit (PICU). A significant reduction in treatment failures (RR 0.50, 95%CI 0.40-0.62) was observed in HFNC versus SOT group1, when two studies (1674 children) were included 2,3. However, there was a significant increase in treatment failures (RR 1.61, 95% CI 1.06-2.42) in HFNC versus nCPAP group1, when two studies (173 children) were included 4,5.
HFNC therapies can be carried out on well-facilitated wards, and the need is greatest during respiratory syncytial virus (RSV) epidemics. The authors concluded that LOS was decreased in the HFNC group in low-income and middle-income countries 1. Even in high-income countries, it is not realistic to treat all bronchiolitis patients, who need oxygen, with HFNC during RSV peaks.
Franklin et al. evaluated HFNC in a RCT including 1472 children with bronchiolitis admitted to 17 hospitals in Australia and New Zealand 2. The primary outcome, treatment failure, happened in 12% of HFNC and in 31% of SOT patients (p<0.001). The figures of failures we...
Lin et al. published a meta-analysis on high-flow nasal cannula therapy (HFNC) in 2121 children with bronchiolitis younger than 24 months1. Six randomised controlled trials (RCTs) compared HFNC with standard oxygen therapy (SOT) and three with nasal continuous positive airway pressure (nCPAP). There were no significant differences in primary outcomes between the groups: length of hospital stay (LOS), length of oxygen supplementation, and transfer to the paediatric intensive care unit (PICU). A significant reduction in treatment failures (RR 0.50, 95%CI 0.40-0.62) was observed in HFNC versus SOT group1, when two studies (1674 children) were included 2,3. However, there was a significant increase in treatment failures (RR 1.61, 95% CI 1.06-2.42) in HFNC versus nCPAP group1, when two studies (173 children) were included 4,5.
HFNC therapies can be carried out on well-facilitated wards, and the need is greatest during respiratory syncytial virus (RSV) epidemics. The authors concluded that LOS was decreased in the HFNC group in low-income and middle-income countries 1. Even in high-income countries, it is not realistic to treat all bronchiolitis patients, who need oxygen, with HFNC during RSV peaks.
Franklin et al. evaluated HFNC in a RCT including 1472 children with bronchiolitis admitted to 17 hospitals in Australia and New Zealand 2. The primary outcome, treatment failure, happened in 12% of HFNC and in 31% of SOT patients (p<0.001). The figures of failures were 33% versus 14% (p=0.002) in the RCT made by Kepreotes et al. including 202 Australian bronchiolitis patients 3. Interestingly, 61% of patients with failures in SOT group could be treated with HFNC on the ward in both studies, and finally, less SOT patients than HFNC patients were transferred to the PICUs 2,3. Beginning with SOT and changing to HFNC, if needed, is an effective way to treat children with bronchiolitis who need oxygen supplementation.
Paula Heikkilä, Matti Korppi
Center for Child Health Research,
Tampere University and University Hospital, Tampere, Finland
References:
1. Lin J, Zhang Y, Xiong L, et al. High-flow nasal cannula therapy for children with bronchiolitis: a systematic review and meta-analysis. Arch Dis Child Epub ahead of print: 17 Jan 2019.
2. Franklin D, Babl FE, Schlapbach LJ, et al. A Randomized Trial of High-Flow Oxygen Therapy in Infants with Bronchiolitis. N Engl J Med. 2018; 378: 1121-1131.
3. Kepreotes E, Whitehead B, Attia J, et al. High-flow warm humidified oxygen versus standard low-flow nasal cannula oxygen for moderate bronchiolitis (HFWHO RCT): an open, phase 4, randomised controlled trial. Lancet. 2017; 389: 930-939.
4. Milesi C, Essouri S, Pouyau R, et al. High flow nasal cannula (HFNC) versus nasal continuous positive airway pressure (nCPAP) for the initial respiratory management of acute viral bronchiolitis in young infants: a multicenter randomized controlled trial (TRAMONTANE study). Intensive Care Med. 2017; 43: 209-216.
5. Sarkar M, Sinha R, Roychowdhoury S, et al. Comparative Study between Noninvasive Continuous positive airway pressure and hot humidified high-flow nasal cannulae as a mode of respiratory support in infants with acute bronchiolitis in pediatric intensive care unit of a tertiary care hospital. Indian J Crit Care Med. 2018; 22: 85-90.
We read with interest the recent article published by Binder E et al. [1], describing the HLA-DQ analysis performed in 1624 asymptomatic children affected with type I Diabetes Mellitus (DMT1), in order to assess their predisposition to develop Celiac Disease (CD). They reported that 1344 (82.8%) patients resulted to be "HLA-DQ2 and/or -DQ8 positive", whereas 280 (17.2%) were negative: among the former group, a biopsy-proven CD diagnosis was documented in 3.6% of cases and, interestingly, even 7 patients in the second group (corresponding to 2.5%) resulted to be celiac. [1]
Thus, these two percentages are not so different and one might conclude that the HLA-DQ asset is not a necessary - even if not sufficient - genetic background, contrary to what is well known. [2] Indeed, the absence of alleles coding MHC-DQ2 and/or MHC-DQ8 heterodimers, is associated with an almost absolute negative predictive value with respect to CD. Therefore, in order to solve this apparent mismatch, it would be useful if the authors can show the complete and high-resolution HLA-DQA1 and, in particular, HLA-DQB1 typing: indeed, these 7 “HLA-DQ2 and/or -DQ8 negative” CD children may not carry all alleles coding any complete MHC-DQ2 and/or MHC-DQ8 molecule, but they may have one or two allelic variants conferring CD risk anyway, such as HLA-DQB1*02, which codes the beta chain of MHC-DQ2 heterodimer. Indeed, according to several studies, the isolate presence of one or two copies of this...
We read with interest the recent article published by Binder E et al. [1], describing the HLA-DQ analysis performed in 1624 asymptomatic children affected with type I Diabetes Mellitus (DMT1), in order to assess their predisposition to develop Celiac Disease (CD). They reported that 1344 (82.8%) patients resulted to be "HLA-DQ2 and/or -DQ8 positive", whereas 280 (17.2%) were negative: among the former group, a biopsy-proven CD diagnosis was documented in 3.6% of cases and, interestingly, even 7 patients in the second group (corresponding to 2.5%) resulted to be celiac. [1]
Thus, these two percentages are not so different and one might conclude that the HLA-DQ asset is not a necessary - even if not sufficient - genetic background, contrary to what is well known. [2] Indeed, the absence of alleles coding MHC-DQ2 and/or MHC-DQ8 heterodimers, is associated with an almost absolute negative predictive value with respect to CD. Therefore, in order to solve this apparent mismatch, it would be useful if the authors can show the complete and high-resolution HLA-DQA1 and, in particular, HLA-DQB1 typing: indeed, these 7 “HLA-DQ2 and/or -DQ8 negative” CD children may not carry all alleles coding any complete MHC-DQ2 and/or MHC-DQ8 molecule, but they may have one or two allelic variants conferring CD risk anyway, such as HLA-DQB1*02, which codes the beta chain of MHC-DQ2 heterodimer. Indeed, according to several studies, the isolate presence of one or two copies of this allelic variant resulted to be associated with significant CD risk, regardless of the concomitant presence of the appropriate HLA-DQA1 allele (*05) necessary to produce a complete MHC-DQ2 molecule. [3-4]
References
1- Binder E, Rohrer T, Denzer C, et al. Screening for coeliac disease in 1624 mainly asymptomatic children with type 1 diabetes: is genotyping for coeliac-specific human leucocyte antigen the right approach? Arch Dis Child. 2018; [Epub ahead of print].
2- Lebwohl B, Sanders DS, Green PHR. Coeliac disease. Lancet. 2018; 391(10115):70-81.
3- De Silvestri A, Capittini C, Poddighe D, et al. HLA-DQ genetics in children with celiac disease: a meta-analysis suggesting a two-step genetic screening procedure starting with HLA-DQ β chains. Pediatr Res. 2018; 83(3):564-572.
4- Megiorni F, Pizzuti A. HLA-DQA1 and HLA-DQB1 in Celiac disease predisposition: practical implications of the HLA molecular typing. J Biomed Sci 2012;19:88.
Many thanks for your response to the editorial ‘What are you looking at?’, which highlights some important principles for this extensively studied research area (despite being a relatively new field in healthcare) [1]
Despite the emergence of new methods to analyse gaze behaviour terminology has not been revised to reflect scientific advances. A recent article by Hessels et al. outlined significant inconsistencies in the definitions of fixations and saccades held by eye movement researchers and highlighted the conceptual confusion surrounding these terms.[2]
The term saccade is derived from the French for ‘jerk’. The phrase appears to have been coined by Emile Javal, a French ophthalmologist, in the 1800’s.[3] By 1916 it had been accepted into the English literature.[4]
Saccades are frequently defined in the literature as rapid, ballistic movements of the eyes that abruptly change the point of fixation.5 Definitions have included;
‘Rapid eye movements used to voluntarily move gaze from one target of interest to another.’[6]
‘Ballistic movements, 20-150ms long, reaching a velocity up to 800°/s. They direct the eye so that external visual objects are projected onto the fovea.’[7]
‘Rapid eye movements used in repositioning the fovea to a new location in the visual environment.’[8]
The term ballistic refers to the fact that the saccade-generating system cannot respond to subsequent changes in the position of a target during th...
Many thanks for your response to the editorial ‘What are you looking at?’, which highlights some important principles for this extensively studied research area (despite being a relatively new field in healthcare) [1]
Despite the emergence of new methods to analyse gaze behaviour terminology has not been revised to reflect scientific advances. A recent article by Hessels et al. outlined significant inconsistencies in the definitions of fixations and saccades held by eye movement researchers and highlighted the conceptual confusion surrounding these terms.[2]
The term saccade is derived from the French for ‘jerk’. The phrase appears to have been coined by Emile Javal, a French ophthalmologist, in the 1800’s.[3] By 1916 it had been accepted into the English literature.[4]
Saccades are frequently defined in the literature as rapid, ballistic movements of the eyes that abruptly change the point of fixation.5 Definitions have included;
‘Rapid eye movements used to voluntarily move gaze from one target of interest to another.’[6]
‘Ballistic movements, 20-150ms long, reaching a velocity up to 800°/s. They direct the eye so that external visual objects are projected onto the fovea.’[7]
‘Rapid eye movements used in repositioning the fovea to a new location in the visual environment.’[8]
The term ballistic refers to the fact that the saccade-generating system cannot respond to subsequent changes in the position of a target during the course of an eye movement. If the target was to move a second saccade would be required to correct the error. Acceptance of such definitions suggests that the primary function of saccades is to bring objects of interest onto or near the fovea. The fovea operates at high resolution and, although it only provides 1-2 degrees of vision, it plays a central role in resolving objects. Whilst saccades assist vision by moving the eyes rapidly to various objects of interest so that parts of a scene can be seen in greater resolution, there is probably little or no meaningful information absorbed during the saccadic movements.
However, other papers have been more liberal in their definitions defining a saccade as the inter-fixation interval.[9,10] These definitions imply that a saccade is any movement outside of periods of fixation. This definition will therefore also capture smooth pursuit movements (slower tracking movements), vestibulo-ocular movements (stabilise eyes relative to external world) and visual scanning movements. Consequentially during saccades defined in this manner visual information may be absorbed both consciously and/or subconsciously including, for example, the presence or absence of pathology, as outlined in your letter.
As the field of eye tracking research in healthcare expands it is imperative that authors explicitly define their key measurements, including fixations, dwell time and saccades, to allow accurate interpretation and comparison of results and to minimise ambiguity. Without this it will be difficult to examine the links between visual scanning patterns and decision making. For example it may be hypothesised that subconscious visual scanning behaviours may be a clue to understanding the concept of gut feeling, whereby a particular clinician sees things perhaps others do not.
We certainly agree greater understanding of saccade pathways should undoubtedly be an area for future research in eye tracking studies in healthcare.
References:
1. Roland D. What are you looking at? Arch Dis Child 2018; 103: 1098-1099.
2. Hessels RS, Niehorster DC, Nyström M, Andersson R, Hooge IT. Is the eye-movement field confused about fixations and saccades? A survey among 124 researchers. Royal Society open science. 2018 Aug 29;5(8):180502.
3. Javal E. Essai sur la physiologie de la lecture. Annales d'Ocilistique. 1878;80:61-73.
4. Wade NJ. Scanning the seen: Vision and the origins of eye-movement research. In Eye Movements 2007 (pp. 31-63).
5. Purves D, Augustine GJ, Fitzpatrick D, Katz LC, LaMantia AS, McNamara JO, Williams SM. Neuroscience 2nd Edition. Sunderland (MA) Sinauer Associates.
6. Ramat S, Leigh RJ, Zee DS, Optican LM. What clinical disorders tell us about the neural control of saccadic eye movements. Brain. 2006 Nov 21;130(1):10-35.
7. Falkmer T, Dahlman J, Dukic T, Bjällmark A, Larsson M. Fixation identification in centroid versus start-point modes using eye-tracking data. Perceptual and motor skills. 2008 Jun;106(3):710-24.
8. Duchowski AT. Eye tracking methodology. Theory and practice. 2007;328.
9. Holmqvist K, Nyström M, Andersson R, Dewhurst R, Jarodzka H, Van de Weijer J. Eye tracking: A comprehensive guide to methods and measures. OUP Oxford; 2011 Sep 22.
10. Larsson L, Nyström M, Andersson R, Stridh M. Detection of fixations and smooth pursuit movements in high-speed eye-tracking data. Biomedical Signal Processing and Control. 2015 Apr 1;18:145-52.
Hall and Sowdon regret that the Newborn Infant Physical Examination (NIPE)/child health surveillance (CHS) programme fails to deliver improved outcomes for developmental dysplasia of the hip (DDH), contrasting with the success of other screening programmes. I would like to make some proposals for improvement.
Current NIPE standards are focused on timeliness of the screening pathway and explicitly exclude treatment outcomes as ‘outside the screening pathway’1. Yet potential outcome measures are routinely available for three of the four NIPE screening programmes and shown to be measurable for two of these. McAllister et have demonstrated that records of surgical intervention for DDH can be used to show variation in outcomes2. Similarly, the NHS Atlas of Variation has demonstrated that age at orchidopexy can be used for undescended testis (UDT)3. Surgery for congenital cataract could be used in the same way. While I accept that definitions and actual measures might need some discussion to reach a national consensus, measuring these outcomes is possible from routine data.
McAllister et al conclude that dedicated leadership of the DDH screening programme is associated with improved outcomes. This has also been shown for UDT4. Unfortunately, clinical leadership of the Healthy Child Programme (HCP) has been dismantled in recent years and the RCPCH recorded a community paediatric HCP lead in only 16% of services in 2015.
Hall and Sowdon regret that the Newborn Infant Physical Examination (NIPE)/child health surveillance (CHS) programme fails to deliver improved outcomes for developmental dysplasia of the hip (DDH), contrasting with the success of other screening programmes. I would like to make some proposals for improvement.
Current NIPE standards are focused on timeliness of the screening pathway and explicitly exclude treatment outcomes as ‘outside the screening pathway’1. Yet potential outcome measures are routinely available for three of the four NIPE screening programmes and shown to be measurable for two of these. McAllister et have demonstrated that records of surgical intervention for DDH can be used to show variation in outcomes2. Similarly, the NHS Atlas of Variation has demonstrated that age at orchidopexy can be used for undescended testis (UDT)3. Surgery for congenital cataract could be used in the same way. While I accept that definitions and actual measures might need some discussion to reach a national consensus, measuring these outcomes is possible from routine data.
McAllister et al conclude that dedicated leadership of the DDH screening programme is associated with improved outcomes. This has also been shown for UDT4. Unfortunately, clinical leadership of the Healthy Child Programme (HCP) has been dismantled in recent years and the RCPCH recorded a community paediatric HCP lead in only 16% of services in 2015.
Lastly poor outcomes may indicate a lack of training. The DDH and UDT examples describe multifaceted interventions including training and support of practitioners. Health visitor training now concentrates on health promotion and safeguarding with a reduced emphasis on child development and clinical skills. There are no longer any specific training requirements for general practitioners (GPs) who perform CHS. This is concerning as we know that only a proportion of GPs have any dedicated training in paediatrics before entering general practice.
There are, therefore, a series of proven measures that, if implemented, could improve the programmes’ performance.
References
1. Public Health England. Our approach to newborn and infant physical examination screening standards. 2018 https://www.gov.uk/government/publications/newborn-and-infant-physical-e... (accessed 11.01.19)
2. McAllister D A, Morling JR, Fischbacher C M et al. Enhanced detection services for developmental dysplasia of the hip in Scottish children 1997 – 2013. Arch Dis Child 2018; 103: 1021 – 1026.
3. Child and Maternal Health Observatory. NHS Atlas of Variation in Healthcare of Children and Young People. 2012. Ch Map 25 Proportion (%) of all elective orchidopexy procedures performed before the age of 2 years by PCT 2007/08–2009/10 p.68-69. Available at https://fingertips.phe.org.uk/profile/atlas-of-variation
4. Brown JJ, Wacogne I, Fleckney S, et al. Achieving early surgery for undescended testes: quality improvement through a multi-faceted approach to guideline implementation. Child: care, health and development 2004; 30: 97–102.
5. Royal College of Paediatrics and Child Health. RCPCH Medical Workforce Census 2015. London 2017. Available at https://www.rcpch.ac.uk/resources/workforce-census-2015 .
We thank Nitzan et al for their comments in relation to our article on use of pulsatility index (PI) in screening for critical congenital heart disease (Searle 2018). In particular, we are grateful that they draw further attention to the potential for current screening to miss critical lesions, such as coarctation of the aorta. Given the progressive nature of these pathologies, it is an extremely difficult challenge to design an acceptable screening tool, which highlights all affected babies in appropriate time. Despite strong biological plausibility, current evidence is unclear whether pulsatility index can translate into such a tool.
We fully agree that the local quality of both antenatal and postnatal screening significantly affects the measured benefit of pulsatility index. Several articles draw the distinction here between ‘tertiary’ and ‘non-tertiary’ units, though it may be more accurate to distinguish ‘better resourced’ from ‘less resourced’ settings, particularly in relation to antenatal scanning. As described in our original article, the apparent potential of PI screening in ‘less resourced’ settings seems strong, especially since many pulse oximetry sensors already measure it. Both Schena et al (2017) and Granelli & Ostman-Smith (2007) highlight a small but important population of babies not detected by standard screening, but with abnormal pre-morbid pulsatility indices. It seems incongruous, however, to extrapolate a single extra case detected by th...
We thank Nitzan et al for their comments in relation to our article on use of pulsatility index (PI) in screening for critical congenital heart disease (Searle 2018). In particular, we are grateful that they draw further attention to the potential for current screening to miss critical lesions, such as coarctation of the aorta. Given the progressive nature of these pathologies, it is an extremely difficult challenge to design an acceptable screening tool, which highlights all affected babies in appropriate time. Despite strong biological plausibility, current evidence is unclear whether pulsatility index can translate into such a tool.
We fully agree that the local quality of both antenatal and postnatal screening significantly affects the measured benefit of pulsatility index. Several articles draw the distinction here between ‘tertiary’ and ‘non-tertiary’ units, though it may be more accurate to distinguish ‘better resourced’ from ‘less resourced’ settings, particularly in relation to antenatal scanning. As described in our original article, the apparent potential of PI screening in ‘less resourced’ settings seems strong, especially since many pulse oximetry sensors already measure it. Both Schena et al (2017) and Granelli & Ostman-Smith (2007) highlight a small but important population of babies not detected by standard screening, but with abnormal pre-morbid pulsatility indices. It seems incongruous, however, to extrapolate a single extra case detected by the Schena et al (2017) study into a real 50% improvement in detection rates, over pulse oximetry screening alone. With such small numbers, the difference between an important finding and statistical or technical anomaly is impossible to determine. We hope this clarifies our original statement that ‘current evidence does not support inclusion of PI into newborn screening’.
Moving forward, the inclusion of pulsatility index within current screening practice would require further large population studies, particularly looking at babies within ‘less resourced’ settings. To make such a study acceptable, the methodology must either i) reduce the high false-positive rate (typically 5%) associated with previous approaches or ii) have robust and pragmatic mechanisms to safely minimise the impact of a false-positive screen on a newborn and their family. Use of different technologies may address the former requirement. Pre-to-post ductal pulse delay, for example, is an innovative approach, though it is untested within a screening context (Palmeri 2017). Within this study, all ‘case’ group babies already demonstrated significant clinical signs at time of testing. Similarly, Nitzan et al’s suggestion to repeat PI measurement after a few days has merit. Establishing the optimal timing of measurements however would be a challenge, to maximise detection without missing early cases. Granelli & Ostman-Smith (2007) could not answer this point, despite study of 10,000 babies up to day 5 of life.
It seems unacceptable to remain in the status quo, where a significant portion of babies are only detected following life-threatening collapse. PI could be an important addition to the screening armoury in ‘low resourced’ settings, but true population-specific evidence would be needed. We very much welcome an open discussion of how to overcome the challenges this would pose.
REFERENCES
Granelli A, Ostman-Smith I. Noninvasive peripheral perfusion index as a possible tool for screening for critical left heart obstruction. Acta Paediatr. 2007;96:1455–9
Palmeri L, Gradwohl G, Nitzan M, et al. Photoplethysmographic waveform characteristics of newborns with coarctation of the aorta. J Perinatol. 2017;37:77–80
Schena F, Picciolli I, Agosti M, et al. Perfusion index and pulse oximetry screening for congenital heart defects. J Pediatr. 2017;183:74–9
Carter et al1 present interesting results which are anecdotally replicated by our local experience and is likely to be played out on a daily basis throughout the country. They conclude that there is a benefit of having senior doctors on the front line at all times when following the NICE guidelines as the majority of febrile children can be safely managed expectantly rather than with tests and treatments with a significant cost and convenience benefit. Whilst no one would doubt the benefit of having experienced doctors on the front line as much as possible- this is often not always practical given the current workforce situation.
A different interpretation would be that this study shows that if the NICE guidelines were followed without senior involvement over 75% of children with fever would be subject to unnecessary investigations and treatment with the attendant risks – physical, experiential and financial to both patients and system. This study shows that widespread deviation from the basic guideline is safe and prudent.
Recognising a sick child is hard whereas recognising a child who is going to become sick is almost impossible as illustrated by the numerous attempts to provide a scoring system or table that might do this. Illness is a process and each child will present at different stages. Paediatricians may be divided into those who have never sent home a child that has returned moribund or worse a few days later and those who have not done so yet....
Carter et al1 present interesting results which are anecdotally replicated by our local experience and is likely to be played out on a daily basis throughout the country. They conclude that there is a benefit of having senior doctors on the front line at all times when following the NICE guidelines as the majority of febrile children can be safely managed expectantly rather than with tests and treatments with a significant cost and convenience benefit. Whilst no one would doubt the benefit of having experienced doctors on the front line as much as possible- this is often not always practical given the current workforce situation.
A different interpretation would be that this study shows that if the NICE guidelines were followed without senior involvement over 75% of children with fever would be subject to unnecessary investigations and treatment with the attendant risks – physical, experiential and financial to both patients and system. This study shows that widespread deviation from the basic guideline is safe and prudent.
Recognising a sick child is hard whereas recognising a child who is going to become sick is almost impossible as illustrated by the numerous attempts to provide a scoring system or table that might do this. Illness is a process and each child will present at different stages. Paediatricians may be divided into those who have never sent home a child that has returned moribund or worse a few days later and those who have not done so yet.
Expecting the NICE, or other guidelines to provide the holy grail of predicting every child that will become sick is a holy grail that does disservice to patients and clinicians alike. Furthermore given that every complaint and medicolegal case asks for reference to established guidelines, all practice is invariably judged against these guidelines and any variation may be presented as poor practice.
If the NICE guidelines were measured as other screening tools, their poor sensitivity would lead to an early jettisoning. Maybe we should recognise that we just don't have the right tools as yet, as a minimum some clear statement as to their effectiveness should be published by NICE.
Whilst no one would contend the benefits of a senior medical presence at all times this should be justified to provide good care rather than mitigate against the overtreatment that would be driven by the NICE guidelines in the absence of these senior doctors, recognising a sick child is hard – how good are we at recognising a sick guideline.
1. Carter MJ, Stilwell PA, Nijman RG, et al. Identification and treatment of paediatric sepsis: getting the balance right
Archives of Disease in Childhood Published Online First: 25 May 2018. doi: 10.1136/archdischild-2018-314865 Letters 20 November, 2018
M Nadeem
1. Department of Paediatrics, Tallaght University Hospital, Dublin 24, Ireland
2. Trinity College Dublin
Corresponding author: M Nadeem, Department of Paediatrics, Tallaght University Hospital, Dublin 24, Ireland
So et al1 reported a case of meningococcal group W meningitis in an infant who presented within 24 hours of receiving group B meningococcal vaccine (4CMenB). Fever and focal seizure, which required two doses of intravenous lorazepam, have been reported at the time of presentation. Intravenous ceftriaxone was commenced for suspected sepsis. CSF PCR was positive for capsular group W meningococcus. With respect to the focal seizure in a febrile infant, whether viral encephalitis was excluded and whether antiviral was commenced pending the exclusion of herpes simplex encephalitis (HSE) are questions that were not addressed in the present case.
At the time of presentation, it may not be possible to clinically differentiate encephalitis from meningitis, as either syndrome may have common features including fever, headache and meningism.2 Children with encephalitis may present with fever, seizures and focal neurological signs.2 3 Moreover those with HSE may experience a progressively deteriorating level of consciousness with fever, focal seizures or focal neurological abnormalities in the absence of any other cause.2 4 However the absence of fever2 5 or the lack of altered states of consciousness5 at presentation does not exclude...
M Nadeem
1. Department of Paediatrics, Tallaght University Hospital, Dublin 24, Ireland
2. Trinity College Dublin
Corresponding author: M Nadeem, Department of Paediatrics, Tallaght University Hospital, Dublin 24, Ireland
So et al1 reported a case of meningococcal group W meningitis in an infant who presented within 24 hours of receiving group B meningococcal vaccine (4CMenB). Fever and focal seizure, which required two doses of intravenous lorazepam, have been reported at the time of presentation. Intravenous ceftriaxone was commenced for suspected sepsis. CSF PCR was positive for capsular group W meningococcus. With respect to the focal seizure in a febrile infant, whether viral encephalitis was excluded and whether antiviral was commenced pending the exclusion of herpes simplex encephalitis (HSE) are questions that were not addressed in the present case.
At the time of presentation, it may not be possible to clinically differentiate encephalitis from meningitis, as either syndrome may have common features including fever, headache and meningism.2 Children with encephalitis may present with fever, seizures and focal neurological signs.2 3 Moreover those with HSE may experience a progressively deteriorating level of consciousness with fever, focal seizures or focal neurological abnormalities in the absence of any other cause.2 4 However the absence of fever2 5 or the lack of altered states of consciousness5 at presentation does not exclude encephalitis. Neuroimaging is a key part of the investigation of a child presenting with encephalitis2, albeit cerebral CT2 or MRI scans6 can be unremarkable in the first days of the disease.
HSE is rare and the long-term consequences can be devastating in cases where therapy is commenced late.7 In those with suspected encephalitis, it was recommended that broad-spectrum antimicrobials and antiviral treatment should be initiated pending the results of diagnostic studies.7
Therefore considering the fever and the focal seizure that require two doses of intravenous lorazepam in the present case, it would be beneficial if the authors address the questions that whether viral encephalitis was excluded and whether antiviral was commenced pending the exclusion of encephalitis.
References:
1. So N, Pal R, Snape MD. Meningococcal meningitis presenting postinfant group B meningococcal immunisation. Archives of Disease in Childhood Published Online First: 05 December 2018. doi: 10.1136/archdischild-2018-316341
2. Thompson C, Kneen R, Riordan A, et al. Encephalitis in children. Archives of Disease in Childhood 2012;97:150-161.
3. Kolski H1, Ford-Jones EL, Richardson S, et al. Etiology of acute childhood encephalitis at The Hospital for Sick Children, Toronto, 1994-1995.
Clin Infect Dis. 1998 Feb;26(2):398-409.
4. Le Doare K, Menson E, Patel D, et al. Fifteen minute consultation: Managing neonatal and childhood herpes encephalitis. Archives of Disease in Childhood - Education and Practice 2015;100:58-63.
5. De Tiège X1, Rozenberg F, Burlot K, et al. Herpes simplex encephalitis: diagnostic problems and late relapse. Dev Med Child Neurol. 2006;48(1):60-3.
6. Hariri OR, Prakash L, Amin J, et al. Atypical presentation of herpes simplex encephalitis in an infant. J Am Osteopath Assoc. 2010;110(10):615-7.
The review by Searle et al “Does pulsatility index add value to newborn pulse oximetry screening for critical congenital heart disease?" (Searle 2018), provides a comprehensive overview of the current evidence regarding the addition of perfusion index to the CCHD screening algorithm.
The authors’ main concern is that adding pulsatility index (perfusion index, PI) will not significantly improve the current detection rate which is already quite high. As a proof, they cite the work of the large trial by Schena et al, (Schena 2017) that found one additional case of CCHD in 42,169 babies examined. The authors conclude that incorporating PI into current screening algorithms provides little additional benefit in detecting CCHD and confers a high false positive rate.
We would like to voice several comments regarding this article:
First, in the study of Schena et al, CCHD was suspected before screening in 36/38 cases in tertiary centers. This is the main reason that PI (and pulse oximetry screening) did not have any additional value in tertiary centers. In this study, only 23.6% of the neonates were born in non-tertiary center. We suggest that an alternative way to describe the results is that in non-tertiary centers, pulse oximetry detected 2 cases and PI detected an additional 1 case per approximately 10,000 screened neonates. Therefore, adding PI to the screening algorithm improved the detection rate by 50%. Moreover, the 2 cases detected by pulse oximetry...
The review by Searle et al “Does pulsatility index add value to newborn pulse oximetry screening for critical congenital heart disease?" (Searle 2018), provides a comprehensive overview of the current evidence regarding the addition of perfusion index to the CCHD screening algorithm.
The authors’ main concern is that adding pulsatility index (perfusion index, PI) will not significantly improve the current detection rate which is already quite high. As a proof, they cite the work of the large trial by Schena et al, (Schena 2017) that found one additional case of CCHD in 42,169 babies examined. The authors conclude that incorporating PI into current screening algorithms provides little additional benefit in detecting CCHD and confers a high false positive rate.
We would like to voice several comments regarding this article:
First, in the study of Schena et al, CCHD was suspected before screening in 36/38 cases in tertiary centers. This is the main reason that PI (and pulse oximetry screening) did not have any additional value in tertiary centers. In this study, only 23.6% of the neonates were born in non-tertiary center. We suggest that an alternative way to describe the results is that in non-tertiary centers, pulse oximetry detected 2 cases and PI detected an additional 1 case per approximately 10,000 screened neonates. Therefore, adding PI to the screening algorithm improved the detection rate by 50%. Moreover, the 2 cases detected by pulse oximetry did not have ductal dependent systemic circulation. Therefore, the most important detection in this study was by PI. We agree with the authors that pulse oximetry CCHD screening, with or without PI, has a low detection rate in tertiary units. However, we believe that this study demonstrates the potential utility of PI as a supplementary screening method in non-tertiary units. This information may be of value in regions with limited access to fetal diagnosis which is expensive and requires advanced technical skills while PI is inexpensive and may be performed by nurses and midwives.
Second, we would like to draw attention to the three missed cases of critical left-sided obstruction described in this study. Two of the neonates presented with signs of shock and cardiac failure. We believe that the current screening algorithms may be improved by measuring the pulse wave delay between extremities (Palmeri 2017) as was mentioned in the review. Detection rates may also increase by improving the method of derivation of PI and by comparing pre and post-ductal PI values (Palmeri 2017, Nitzan 2018). Another option that may be relevant in some regions, is a repeated screening test performed in the community clinic or during a home visit after hospital discharge in the hope of detecting critical left-sided obstruction during the process of duct closure before the onset of cardiac failure.
We thank the authors for raising awareness of this important question, and we hope that future studies will address this issue.
Searle J, Thakkar DD, Banerjee J.Does pulsatility index add value to newborn pulse oximetry screening for critical congenital heart disease? Arch Dis Child. 2018 Nov 9. pii: archdischild-2018-315891. doi: 10.1136/archdischild-2018-315891. [Epub ahead of print]
Schena F, Picciolli I, Agosti M, et al. Perfusion index and pulse oximetry screening for
congenital heart defects. J Pediatr 2017;183:74–9.
Palmeri L, Gradwohl G, Nitzan M, et al. Photoplethysmographic waveform
characteristics of newborns with coarctation of the aorta. J Perinatol 2017;37:77–80.
Nitzan I, Hammerman C, Fink D, Nitzan M, Koppel R, Bromiker R. The effect of patent ductus arteriosus on pre-ductal and post-ductal perfusion index in preterm neonates. Physiol Meas. 2018 Jul 20;39(7):075006. doi: 10.1088/1361-6579/aacf25.
Seo et al. conducted a prospective study to identify factors for cardiovascular disease risk factor clustering (CVD-RFC) in adolescents (1). A total of 1309 children aged 6-15 years were enrolled, and higher household income was a significant predictor of lower CVD-RFC incidence with dose-response relationship. In contrast, the presence of parental CVD history, overweight or obesity, and shorter sleep duration were significant predictors of higher CVD-RFC incidence. I have some comments with special reference to socioeconomic status (SES) and metabolic components.
First, Iguacel et al. investigated the association between socioeconomic disadvantages and metabolic syndrome (MetS) in children (2). By adjusting diet, physical activity, sedentary behaviours and well-being, standardized multiple regression coefficients (99% confidence intervals [CI]) of children from low-income families, non-traditional families, with parents of unemployment, and accumulation of >3 socioeconomic disadvantages for a higher MetS score were 0.20 (0.03-0.37), 0.14 (0.02-0.26), 0.31 (0.05-0.57), 0.21 (0.04-0.37), respectively. These data present that low SES was closely associated with MetS in children, which was in concordance with data by Seo et al (1).
Second, Patel et al. examined the association between parental socioeconomic position (SEP) and early-life offspring body mass index (BMI) in children (3). Adjusted difference of BMI z-score (95% CI) was 0.08 (0-0.16) among girls...
Seo et al. conducted a prospective study to identify factors for cardiovascular disease risk factor clustering (CVD-RFC) in adolescents (1). A total of 1309 children aged 6-15 years were enrolled, and higher household income was a significant predictor of lower CVD-RFC incidence with dose-response relationship. In contrast, the presence of parental CVD history, overweight or obesity, and shorter sleep duration were significant predictors of higher CVD-RFC incidence. I have some comments with special reference to socioeconomic status (SES) and metabolic components.
First, Iguacel et al. investigated the association between socioeconomic disadvantages and metabolic syndrome (MetS) in children (2). By adjusting diet, physical activity, sedentary behaviours and well-being, standardized multiple regression coefficients (99% confidence intervals [CI]) of children from low-income families, non-traditional families, with parents of unemployment, and accumulation of >3 socioeconomic disadvantages for a higher MetS score were 0.20 (0.03-0.37), 0.14 (0.02-0.26), 0.31 (0.05-0.57), 0.21 (0.04-0.37), respectively. These data present that low SES was closely associated with MetS in children, which was in concordance with data by Seo et al (1).
Second, Patel et al. examined the association between parental socioeconomic position (SEP) and early-life offspring body mass index (BMI) in children (3). Adjusted difference of BMI z-score (95% CI) was 0.08 (0-0.16) among girls and 0.16 (0.07-0.24) among boys, and they concluded that higher SEP was associated with greater BMI trajectories in both sexes. In contrast, Oddo and Jones-Smith investigated the association between the change of family income and the change of BMI z-score in children (4). The poverty to family income ratio (PIR) and the increase in PIR were significantly associated with decrease in BMI z-score only among girls. Seo et al. did not recognize significant sex difference, but they presented 10% decrease of CVD-RFC in girls. Sex difference should be specified by further study.
Finally, Lee et al. investigate the relationship between SES and obesity in children (5). They used education and income as an indicator of SES, and SES was not a significant indicator for childhood obesity. In contrast, childhood obesity was positively associated with maternal overweight, maternal obesity and paternal obesity. SES had a smaller impact than parental obesity on childhood obesity. Relating to this report, Andrea et al. conducted a systematic review concerning the effect of early life growth (0-24 months of age) on later obesity (>24 months) by considering race/ethnicity and SES (6). They recognized that the positive association was predominant in populations of racial/ethnic minority. A comprehensive analysis is needed to identify the association between SES and CVD-RFC.
References
1 Seo YG, Choi MK, Kang JH, et al. Cardiovascular disease risk factor clustering in children and adolescents: a prospective cohort study. Arch Dis Child 2018;103:968-73
2 Iguacel I, Michels N, Ahrens W, et al. Prospective associations between socioeconomically disadvantaged groups and metabolic syndrome risk in European children. Results from the IDEFICS study. Int J Cardiol 2018:272 :333-40.
3 Patel R, Tilling K, Lawlor DA, et al. Socioeconomic differences in childhood BMI trajectories in Belarus. Int J Obes (Lond) 2018:42:1651-60.
4 Oddo VM, Jones-Smith JC. Gains in income during early childhood are associated with decreases in BMI z scores among children in the United States. Am J Clin Nutr 2015;101:1225-31.
5 Lee HJ, Kim SH, Choi SH, et al. The Association between socioeconomic status and obesity in Korean children: An analysis of the Fifth Korea National Health and Nutrition Examination Survey (2010-2012). Pediatr Gastroenterol Hepatol Nutr 2017;20:186-93.
6 Andrea SB, Hooker ER, Messer LC, et al. Does the association between early life growth and later obesity differ by race/ethnicity or socioeconomic status? A systematic review. Ann Epidemiol 2017;27:583-92.e5.
It is with great interest that we read ‘Why do babies cry?” in which Dr. Robert Scott-Jupp have provided a concise evaluation of the research pertaining to non-pathologic crying in infants.
Crying is a normal variant in the day 2 newborn examination however it can pose a significant source of stress and anxiety for parents. To add to the body of evidence detailed in this article we posed the question; What proportion of babies cry during the day 2 newborn examination?
A convenience sample of data was collected on well babies during the standard day 2 physical examination on the postnatal ward in a tertiary maternity hospital. All babies on the postnatal ward were eligible for inclusion. Gestation, birth weight, gender, mode of delivery and duration of examination were recorded. The presence or absence of crying during examination was documented. The data was analysed using SPSS .
One hundred and fifty three babies (n=153) were included in the study. There were 82 male infants (53%) and 71 female infants (47%). Mean birth weight was 3589g (range 2590g -5160g) with a mean gestation of 39+4 (Range 36+3 - 42+1). Mean duration of examination was 7 minutes. Eighty-one babies (52.9%) delivered by spontaneous vaginal delivery, 22 (14.4%) by ventouse, 26 (16.9%) by elective caesarean section, 20 (13.1%) by emergency caesarean section and 4(2.6%) by forceps. Overall, 118 (77.1%) babies were observed to cry during the physical examination (78%...
It is with great interest that we read ‘Why do babies cry?” in which Dr. Robert Scott-Jupp have provided a concise evaluation of the research pertaining to non-pathologic crying in infants.
Crying is a normal variant in the day 2 newborn examination however it can pose a significant source of stress and anxiety for parents. To add to the body of evidence detailed in this article we posed the question; What proportion of babies cry during the day 2 newborn examination?
A convenience sample of data was collected on well babies during the standard day 2 physical examination on the postnatal ward in a tertiary maternity hospital. All babies on the postnatal ward were eligible for inclusion. Gestation, birth weight, gender, mode of delivery and duration of examination were recorded. The presence or absence of crying during examination was documented. The data was analysed using SPSS .
One hundred and fifty three babies (n=153) were included in the study. There were 82 male infants (53%) and 71 female infants (47%). Mean birth weight was 3589g (range 2590g -5160g) with a mean gestation of 39+4 (Range 36+3 - 42+1). Mean duration of examination was 7 minutes. Eighty-one babies (52.9%) delivered by spontaneous vaginal delivery, 22 (14.4%) by ventouse, 26 (16.9%) by elective caesarean section, 20 (13.1%) by emergency caesarean section and 4(2.6%) by forceps. Overall, 118 (77.1%) babies were observed to cry during the physical examination (78% male vs 76% female). There was no difference in incidence of crying when compared for gestation. Eighty eight percent of babies born by instrumental delivery cried during examination while only 74% of those born by spontaneous vaginal delivery and 76% of those born by emergency section cried. Babies with a birth weight of 4001g – 4500g were more likely to cry than any other birth weight category (90.4%).
To conclude, crying is a normal variant in the newborn examination. Communicating these statistics to parents could play a role in reducing stress and anxiety. This is the first study to document the frequency of crying on the day 2 examination. It was also observed that babies of a higher birth weight, as well as those delivered instrumentally, were more likely to cry than others.
Lin et al. published a meta-analysis on high-flow nasal cannula therapy (HFNC) in 2121 children with bronchiolitis younger than 24 months1. Six randomised controlled trials (RCTs) compared HFNC with standard oxygen therapy (SOT) and three with nasal continuous positive airway pressure (nCPAP). There were no significant differences in primary outcomes between the groups: length of hospital stay (LOS), length of oxygen supplementation, and transfer to the paediatric intensive care unit (PICU). A significant reduction in treatment failures (RR 0.50, 95%CI 0.40-0.62) was observed in HFNC versus SOT group1, when two studies (1674 children) were included 2,3. However, there was a significant increase in treatment failures (RR 1.61, 95% CI 1.06-2.42) in HFNC versus nCPAP group1, when two studies (173 children) were included 4,5.
Show MoreHFNC therapies can be carried out on well-facilitated wards, and the need is greatest during respiratory syncytial virus (RSV) epidemics. The authors concluded that LOS was decreased in the HFNC group in low-income and middle-income countries 1. Even in high-income countries, it is not realistic to treat all bronchiolitis patients, who need oxygen, with HFNC during RSV peaks.
Franklin et al. evaluated HFNC in a RCT including 1472 children with bronchiolitis admitted to 17 hospitals in Australia and New Zealand 2. The primary outcome, treatment failure, happened in 12% of HFNC and in 31% of SOT patients (p<0.001). The figures of failures we...
We read with interest the recent article published by Binder E et al. [1], describing the HLA-DQ analysis performed in 1624 asymptomatic children affected with type I Diabetes Mellitus (DMT1), in order to assess their predisposition to develop Celiac Disease (CD). They reported that 1344 (82.8%) patients resulted to be "HLA-DQ2 and/or -DQ8 positive", whereas 280 (17.2%) were negative: among the former group, a biopsy-proven CD diagnosis was documented in 3.6% of cases and, interestingly, even 7 patients in the second group (corresponding to 2.5%) resulted to be celiac. [1]
Show MoreThus, these two percentages are not so different and one might conclude that the HLA-DQ asset is not a necessary - even if not sufficient - genetic background, contrary to what is well known. [2] Indeed, the absence of alleles coding MHC-DQ2 and/or MHC-DQ8 heterodimers, is associated with an almost absolute negative predictive value with respect to CD. Therefore, in order to solve this apparent mismatch, it would be useful if the authors can show the complete and high-resolution HLA-DQA1 and, in particular, HLA-DQB1 typing: indeed, these 7 “HLA-DQ2 and/or -DQ8 negative” CD children may not carry all alleles coding any complete MHC-DQ2 and/or MHC-DQ8 molecule, but they may have one or two allelic variants conferring CD risk anyway, such as HLA-DQB1*02, which codes the beta chain of MHC-DQ2 heterodimer. Indeed, according to several studies, the isolate presence of one or two copies of this...
Many thanks for your response to the editorial ‘What are you looking at?’, which highlights some important principles for this extensively studied research area (despite being a relatively new field in healthcare) [1]
Despite the emergence of new methods to analyse gaze behaviour terminology has not been revised to reflect scientific advances. A recent article by Hessels et al. outlined significant inconsistencies in the definitions of fixations and saccades held by eye movement researchers and highlighted the conceptual confusion surrounding these terms.[2]
The term saccade is derived from the French for ‘jerk’. The phrase appears to have been coined by Emile Javal, a French ophthalmologist, in the 1800’s.[3] By 1916 it had been accepted into the English literature.[4]
Saccades are frequently defined in the literature as rapid, ballistic movements of the eyes that abruptly change the point of fixation.5 Definitions have included;
‘Rapid eye movements used to voluntarily move gaze from one target of interest to another.’[6]
‘Ballistic movements, 20-150ms long, reaching a velocity up to 800°/s. They direct the eye so that external visual objects are projected onto the fovea.’[7]
‘Rapid eye movements used in repositioning the fovea to a new location in the visual environment.’[8]
The term ballistic refers to the fact that the saccade-generating system cannot respond to subsequent changes in the position of a target during th...
Show MoreHall and Sowdon regret that the Newborn Infant Physical Examination (NIPE)/child health surveillance (CHS) programme fails to deliver improved outcomes for developmental dysplasia of the hip (DDH), contrasting with the success of other screening programmes. I would like to make some proposals for improvement.
Current NIPE standards are focused on timeliness of the screening pathway and explicitly exclude treatment outcomes as ‘outside the screening pathway’1. Yet potential outcome measures are routinely available for three of the four NIPE screening programmes and shown to be measurable for two of these. McAllister et have demonstrated that records of surgical intervention for DDH can be used to show variation in outcomes2. Similarly, the NHS Atlas of Variation has demonstrated that age at orchidopexy can be used for undescended testis (UDT)3. Surgery for congenital cataract could be used in the same way. While I accept that definitions and actual measures might need some discussion to reach a national consensus, measuring these outcomes is possible from routine data.
McAllister et al conclude that dedicated leadership of the DDH screening programme is associated with improved outcomes. This has also been shown for UDT4. Unfortunately, clinical leadership of the Healthy Child Programme (HCP) has been dismantled in recent years and the RCPCH recorded a community paediatric HCP lead in only 16% of services in 2015.
Lastly poor outcomes may indicate...
Show MoreWe thank Nitzan et al for their comments in relation to our article on use of pulsatility index (PI) in screening for critical congenital heart disease (Searle 2018). In particular, we are grateful that they draw further attention to the potential for current screening to miss critical lesions, such as coarctation of the aorta. Given the progressive nature of these pathologies, it is an extremely difficult challenge to design an acceptable screening tool, which highlights all affected babies in appropriate time. Despite strong biological plausibility, current evidence is unclear whether pulsatility index can translate into such a tool.
We fully agree that the local quality of both antenatal and postnatal screening significantly affects the measured benefit of pulsatility index. Several articles draw the distinction here between ‘tertiary’ and ‘non-tertiary’ units, though it may be more accurate to distinguish ‘better resourced’ from ‘less resourced’ settings, particularly in relation to antenatal scanning. As described in our original article, the apparent potential of PI screening in ‘less resourced’ settings seems strong, especially since many pulse oximetry sensors already measure it. Both Schena et al (2017) and Granelli & Ostman-Smith (2007) highlight a small but important population of babies not detected by standard screening, but with abnormal pre-morbid pulsatility indices. It seems incongruous, however, to extrapolate a single extra case detected by th...
Show MoreCarter et al1 present interesting results which are anecdotally replicated by our local experience and is likely to be played out on a daily basis throughout the country. They conclude that there is a benefit of having senior doctors on the front line at all times when following the NICE guidelines as the majority of febrile children can be safely managed expectantly rather than with tests and treatments with a significant cost and convenience benefit. Whilst no one would doubt the benefit of having experienced doctors on the front line as much as possible- this is often not always practical given the current workforce situation.
A different interpretation would be that this study shows that if the NICE guidelines were followed without senior involvement over 75% of children with fever would be subject to unnecessary investigations and treatment with the attendant risks – physical, experiential and financial to both patients and system. This study shows that widespread deviation from the basic guideline is safe and prudent.
Recognising a sick child is hard whereas recognising a child who is going to become sick is almost impossible as illustrated by the numerous attempts to provide a scoring system or table that might do this. Illness is a process and each child will present at different stages. Paediatricians may be divided into those who have never sent home a child that has returned moribund or worse a few days later and those who have not done so yet....
Show MoreM Nadeem
1. Department of Paediatrics, Tallaght University Hospital, Dublin 24, Ireland
2. Trinity College Dublin
Corresponding author: M Nadeem, Department of Paediatrics, Tallaght University Hospital, Dublin 24, Ireland
So et al1 reported a case of meningococcal group W meningitis in an infant who presented within 24 hours of receiving group B meningococcal vaccine (4CMenB). Fever and focal seizure, which required two doses of intravenous lorazepam, have been reported at the time of presentation. Intravenous ceftriaxone was commenced for suspected sepsis. CSF PCR was positive for capsular group W meningococcus. With respect to the focal seizure in a febrile infant, whether viral encephalitis was excluded and whether antiviral was commenced pending the exclusion of herpes simplex encephalitis (HSE) are questions that were not addressed in the present case.
At the time of presentation, it may not be possible to clinically differentiate encephalitis from meningitis, as either syndrome may have common features including fever, headache and meningism.2 Children with encephalitis may present with fever, seizures and focal neurological signs.2 3 Moreover those with HSE may experience a progressively deteriorating level of consciousness with fever, focal seizures or focal neurological abnormalities in the absence of any other cause.2 4 However the absence of fever2 5 or the lack of altered states of consciousness5 at presentation does not exclude...
Show MoreThe review by Searle et al “Does pulsatility index add value to newborn pulse oximetry screening for critical congenital heart disease?" (Searle 2018), provides a comprehensive overview of the current evidence regarding the addition of perfusion index to the CCHD screening algorithm.
Show MoreThe authors’ main concern is that adding pulsatility index (perfusion index, PI) will not significantly improve the current detection rate which is already quite high. As a proof, they cite the work of the large trial by Schena et al, (Schena 2017) that found one additional case of CCHD in 42,169 babies examined. The authors conclude that incorporating PI into current screening algorithms provides little additional benefit in detecting CCHD and confers a high false positive rate.
We would like to voice several comments regarding this article:
First, in the study of Schena et al, CCHD was suspected before screening in 36/38 cases in tertiary centers. This is the main reason that PI (and pulse oximetry screening) did not have any additional value in tertiary centers. In this study, only 23.6% of the neonates were born in non-tertiary center. We suggest that an alternative way to describe the results is that in non-tertiary centers, pulse oximetry detected 2 cases and PI detected an additional 1 case per approximately 10,000 screened neonates. Therefore, adding PI to the screening algorithm improved the detection rate by 50%. Moreover, the 2 cases detected by pulse oximetry...
Seo et al. conducted a prospective study to identify factors for cardiovascular disease risk factor clustering (CVD-RFC) in adolescents (1). A total of 1309 children aged 6-15 years were enrolled, and higher household income was a significant predictor of lower CVD-RFC incidence with dose-response relationship. In contrast, the presence of parental CVD history, overweight or obesity, and shorter sleep duration were significant predictors of higher CVD-RFC incidence. I have some comments with special reference to socioeconomic status (SES) and metabolic components.
First, Iguacel et al. investigated the association between socioeconomic disadvantages and metabolic syndrome (MetS) in children (2). By adjusting diet, physical activity, sedentary behaviours and well-being, standardized multiple regression coefficients (99% confidence intervals [CI]) of children from low-income families, non-traditional families, with parents of unemployment, and accumulation of >3 socioeconomic disadvantages for a higher MetS score were 0.20 (0.03-0.37), 0.14 (0.02-0.26), 0.31 (0.05-0.57), 0.21 (0.04-0.37), respectively. These data present that low SES was closely associated with MetS in children, which was in concordance with data by Seo et al (1).
Second, Patel et al. examined the association between parental socioeconomic position (SEP) and early-life offspring body mass index (BMI) in children (3). Adjusted difference of BMI z-score (95% CI) was 0.08 (0-0.16) among girls...
Show MoreDear Sir,
It is with great interest that we read ‘Why do babies cry?” in which Dr. Robert Scott-Jupp have provided a concise evaluation of the research pertaining to non-pathologic crying in infants.
Crying is a normal variant in the day 2 newborn examination however it can pose a significant source of stress and anxiety for parents. To add to the body of evidence detailed in this article we posed the question; What proportion of babies cry during the day 2 newborn examination?
A convenience sample of data was collected on well babies during the standard day 2 physical examination on the postnatal ward in a tertiary maternity hospital. All babies on the postnatal ward were eligible for inclusion. Gestation, birth weight, gender, mode of delivery and duration of examination were recorded. The presence or absence of crying during examination was documented. The data was analysed using SPSS .
One hundred and fifty three babies (n=153) were included in the study. There were 82 male infants (53%) and 71 female infants (47%). Mean birth weight was 3589g (range 2590g -5160g) with a mean gestation of 39+4 (Range 36+3 - 42+1). Mean duration of examination was 7 minutes. Eighty-one babies (52.9%) delivered by spontaneous vaginal delivery, 22 (14.4%) by ventouse, 26 (16.9%) by elective caesarean section, 20 (13.1%) by emergency caesarean section and 4(2.6%) by forceps. Overall, 118 (77.1%) babies were observed to cry during the physical examination (78%...
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