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1.
Emerg Med Australas ; 30(5): 687-693, 2018 10.
Article in English | MEDLINE | ID: mdl-30021244

ABSTRACT

OBJECTIVE: In paediatric cardiopulmonary arrest, International Liaison Committee on Resuscitation (ILCOR) states, 'there are no simple guidelines to determine when resuscitative efforts become futile'. Considerations to assist this decision-making include cause of arrest, pre-existing medical conditions, age, site of arrest, duration of untreated cardiopulmonary arrest, witnessed arrest and presence of shockable rhythm. Outcomes are poor in out-of-hospital cardiac arrests (OHCA), particularly for infants. This single-centre observational study describes the characteristics and outcomes of the subgroup of children presenting to our hospital's ED following OHCA still receiving cardiac compressions, to assist development of guidelines for future resuscitation efforts in our ED, particularly for cessation of cardiopulmonary resuscitation (CPR). METHODS: The ED database was searched for children presenting in cardiopulmonary arrest receiving cardiac compressions. Data were reviewed on pre-hospital, ED and hospital management and outcome, particularly looking at considerations outlined by ILCOR. RESULTS: From January 2000 to December 2013, 60 children were identified: median age 1.71 years; 87% arresting at home; 68% with bystander CPR; median CPR duration pre-hospital 42 min, and in ED 19.5 min; total CPR median 61 min. Fifty patients (83%) died in ED, 10 (17%) were admitted to intensive care but all died within 4 days. CONCLUSION: Children presenting to ED still receiving cardiac compressions following OHCA had a universally poor outcome, regardless of age and underlying cause. This implies resuscitative efforts could be discontinued earlier in this subgroup. A national, multicentre study is needed to determine if this finding is reproducible with a larger population.


Subject(s)
Emergency Service, Hospital/statistics & numerical data , Out-of-Hospital Cardiac Arrest/mortality , Adolescent , Australia , Child , Child, Preschool , Emergency Medical Services/statistics & numerical data , Emergency Service, Hospital/organization & administration , Female , Humans , Infant , Male , Out-of-Hospital Cardiac Arrest/epidemiology , Pediatrics/instrumentation , Pediatrics/statistics & numerical data , Resuscitation/mortality , Retrospective Studies , Time Factors
2.
Pediatr Nephrol ; 30(8): 1361-5, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25953247

ABSTRACT

BACKGROUND: Middle aortic syndrome (MAS) is an uncommon cause of hypertension in children. The management of hypertension secondary to MAS frequently requires several anti-hypertensive medications along with endovascular and often surgical intervention. CASE-DIAGNOSIS/TREATMENT: A 9-year-old boy presented with headaches and vomiting and was diagnosed with severe hypertension secondary to idiopathic MAS affecting a long segment of the abdominal aorta and left renal artery stenosis. Over the following 8 years his hypertension was successfully managed initially with percutaneous transluminal balloon angioplasty (PTA) of his left renal artery, followed by balloon dilatation of his abdominal aortic narrowing. He subsequently underwent abdominal aortic stent placement following failed repeat aortic balloon dilatation. Aged 17 years and 6 months he is now on a single anti-hypertensive agent with normal renal function and no evidence of target organ damage. CONCLUSION: In selected cases, MAS may be managed with PTA and stent placement with good long-term outcomes. Limited data on the use of PTA and stent insertion in children means that a structured approach to the management of refractory hypertension secondary to MAS remains elusive.


Subject(s)
Aortic Coarctation/complications , Aortic Coarctation/pathology , Aortic Coarctation/physiopathology , Aortic Coarctation/therapy , Hypertension/etiology , Child , Humans , Hypertension/therapy , Male
4.
Nephrol Dial Transplant ; 26(11): 3816-9, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21965587

ABSTRACT

An 11-month-old girl presented with a history of failure to thrive, vomiting, polydipsia, polyuria and visual inattention. She was found to have malignant hypertension due to unilateral renal artery stenosis. This was successfully treated with percutaneous transluminal balloon angioplasty. Nearly 10 years following this initial presentation, she remains normotensive on no anti-hypertensive medications.


Subject(s)
Angioplasty, Balloon , Failure to Thrive/drug therapy , Failure to Thrive/etiology , Hypertension, Malignant/drug therapy , Hypertension, Malignant/etiology , Renal Artery Obstruction/complications , Renal Artery Obstruction/therapy , Antihypertensive Agents/therapeutic use , Female , Humans , Infant
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