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1.
Med Teach ; 34(5): 404-10, 2012.
Article in English | MEDLINE | ID: mdl-22471914

ABSTRACT

BACKGROUND: Competency in the management of acutely unwell patients has not previously been formally assessed as part of an objective structured clinical examination (OSCE). AIM: The reliability of the paediatric postgraduate OSCE was calculated. An objective structured video examination was designed to assess candidates' clinical decision making ability when managing acutely unwell children. METHODS: The performance of 3522 postgraduate paediatric trainees was assessed (2006-2008). OSCE reliability was determined using Cronbach's alpha and mean inter-item correlation. Performance in the video station was compared with overall performance (not including video station; Mann-Whitney U) and video station scores correlated with individual station scores (Spearman's Rho correlation coefficient). RESULTS: Clinical examination pass rates for the 684 UK graduates, 1608 overseas candidates training in the UK and 1104 overseas candidates training overseas were 69.7%, 28% and 22.3%, respectively (graduation information not available for 126 candidates). Cronbach's alpha was 0.62. Mean inter-item correlation was 0.15. Candidates who passed the OSCE overall had significantly higher scores on the video station (t(3520) = 14.48); p < 0.001). There was significant positive correlation between scores on the video station, individual stations and overall total score (r's = 0.300; p = 0.001). CONCLUSIONS: The postgraduate paediatric OSCE provides a sound and valid means of assessing clinical skills at the postgraduate level. The video station provides an important new method of assessment. Its use in other postgraduate clinical examinations should be explored.


Subject(s)
Education, Medical, Continuing/methods , Educational Measurement/methods , Physical Examination/methods , Video Recording , Acute Disease , Child , Decision Support Techniques , Humans , Medical History Taking/methods , Reproducibility of Results , United Kingdom
2.
Arch Dis Child Fetal Neonatal Ed ; 97(4): F299-303, 2012 Jul.
Article in English | MEDLINE | ID: mdl-21427126

ABSTRACT

Postnatal steroids have been widely used to facilitate the extubation of ventilator-dependent preterm infants. Reports published in the late 1990s and early 2000s raised concerns about their long-term impact on neurodevelopmental outcomes. Since then, postnatal steroid use has declined sharply, but they continue to be regarded by many clinicians as an essential part of neonatal care, and there is considerable confusion as to the most appropriate time to use them. This review examines the meta-analyses of the relationship between intravenous postnatal steroids and neurodevelopmental impairment, and provides recommendations for their use based upon that body of evidence.


Subject(s)
Developmental Disabilities/chemically induced , Glucocorticoids/adverse effects , Cerebral Palsy/chemically induced , Chronic Disease , Drug Administration Schedule , Evidence-Based Medicine/methods , Glucocorticoids/administration & dosage , Glucocorticoids/therapeutic use , Humans , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/prevention & control , Injections, Intravenous , Lung Diseases/prevention & control , Prognosis
3.
Arch Dis Child Fetal Neonatal Ed ; 96(3): F190-4, 2011 May.
Article in English | MEDLINE | ID: mdl-21115554

ABSTRACT

OBJECTIVE: Postnatal dexamethasone therapy is controversial. This study aimed to determine the short-term effects of Minidex (low-dose dexamethasone 0.05 mg/kg/day) on ventilator-dependent preterm babies. METHODS: Very preterm babies (less than 30 weeks of gestation or under 1500 g) who were ventilator dependent at over 2 weeks of life and received Minidex therapy (low-dose dexamethasone 0.05 mg/kg/day for 10 days followed by alternate-day doses for 6 days) were compared retrospectively to a matched comparison group who received neither Minidex nor standard-dose dexamethasone. RESULTS: 50 babies who received Minidex were compared to a comparison group of 26 babies. Babies treated with Minidex extubated significantly faster than controls, Cox regression hazard ratio 6.24 (95% CI 2.34 to 16.63). By day 4, 34% of babies treated with Minidex had extubated but no controls had. Babies who received Minidex showed significant improvements in both ventilatory index and oxygen requirements, had no increased rate of clinical hypertension (OR 1.16 (95% CI 0.42 to 3.21)) or hyperglycaemia (OR 1.55 (95% CI 0.44 to 5.45)) and had a similar rate of chronic lung disease at 36 weeks' corrected age (OR 1.61 (95% CI 0.62 to 4.22)). No baby developed gastrointestinal perforation or haemorrhage. CONCLUSION: Minidex therapy facilitates extubation and is not associated with clinically significant short-term side effects. A randomised controlled trial is required to further assess efficacy and long-term outcomes.


Subject(s)
Bronchopulmonary Dysplasia/drug therapy , Dexamethasone/administration & dosage , Glucocorticoids/administration & dosage , Birth Weight , Device Removal , Dexamethasone/adverse effects , Dexamethasone/therapeutic use , Disease Progression , Drug Administration Schedule , Drug Evaluation , Female , Gestational Age , Glucocorticoids/adverse effects , Glucocorticoids/therapeutic use , Humans , Infant, Newborn , Infant, Premature , Intubation, Intratracheal , Male , Retrospective Studies , Time Factors , Ventilator Weaning/methods
4.
Arch Dis Child Fetal Neonatal Ed ; 94(5): F379-83, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19307225

ABSTRACT

Gastrooesophageal reflux disease (GORD) provides a diagnostic and therapeutic challenge to many neonatologists. Reflux of gastric contents is common in preterm infants but usually not pathological. GORD is frequently diagnosed despite the lack of a fully identified clinical syndrome and of a truly valid diagnostic test. Treatment modalities, for which there is little convincing evidence regarding efficacy, are commonly instigated for troublesome symptoms attributed to GORD. Diagnosis is so problematic in preterm infants that GORD is starting to be described as the clinical syndrome that responds to anti-reflux treatment. We discuss the dilemmas facing us when dealing with this condition, summarise the best available evidence regarding diagnosis and management, and use it to inform a suggested treatment pathway. We introduce the concept of a clinical scoring system to aid the diagnosis and monitoring of GORD in preterm infants and highlight areas where further research would be beneficial.


Subject(s)
Gastroesophageal Reflux , Gastrointestinal Agents/therapeutic use , Infant, Premature, Diseases/diagnosis , Gastroesophageal Reflux/diagnosis , Gastroesophageal Reflux/drug therapy , Humans , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/drug therapy , Practice Guidelines as Topic
5.
Clin Lab Haematol ; 28(2): 117-21, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16630216

ABSTRACT

The aim of this validation study was to compare prothrombin time (PT) and activated partial thromboplastin time (APTT) results from a point-of-care testing (POCT) device (Rapidpoint Coag) with those from standard laboratory tests. The subjects were newborn infants needing coagulation screen for any clinical indications within a regional neonatal intensive care unit. The level of agreement between POCT and laboratory measurements of PT and APTT was determined. For PT: the bias was from -7.6 to 12.4 s and precision was 5.0 s. For the detection of prolonged PT at a level of 16 s, the sensitivity was 0.70, specificity was 0.57 and the positive predictive value (PPV) was 0.62. For APTT: the bias was from -39.1 to 23.7 s, and precision was 15.7 s. For the detection of prolonged APTT at a level of 55 s, the sensitivity was 0.80, specificity was 0.95 and the PPV was 0.80. The POCT device tested has limited utility as a cot-side device for screening for a prolongation of the APTT in the newborn but is not sensitive for screening for prolongation of the PT.


Subject(s)
Partial Thromboplastin Time/methods , Point-of-Care Systems , Prothrombin Time/methods , Female , Humans , Infant , Infant, Newborn , Male , Partial Thromboplastin Time/instrumentation , Prothrombin Time/instrumentation
6.
Arch Dis Child ; 91(2): 173-4, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16428365

ABSTRACT

Groups of 25 children with cerebral palsy (CP), inflammatory bowel disease (IBD), and cancer were compared to 25 healthy children to establish use of complementary or alternative medicine (CAM). Children with chronic disease were greater than three times more likely to use CAM, usually without paediatricians' knowledge.


Subject(s)
Chronic Disease/therapy , Complementary Therapies/statistics & numerical data , Patient Acceptance of Health Care/statistics & numerical data , Adolescent , Cerebral Palsy/therapy , Child , Child, Preschool , England , Female , Humans , Infant , Inflammatory Bowel Diseases/therapy , Male , Neoplasms/therapy , Poverty
7.
Pediatr Hematol Oncol ; 22(7): 551-9, 2005.
Article in English | MEDLINE | ID: mdl-16166047

ABSTRACT

The authors aimed to test the hypothesis that blood transfusions depress hematopoiesis in healthy infants with anemia of prematurity (AOP). They also set out to find markers that predict recovery from AOP. Thirty-nine premature babies underwent weekly and post-transfusion measurements of hemoglobin concentrations, reticulocyte counts (RCC), and erythropoietin levels (EPO). RCC and EPO dropped significantly 7 days after a blood transfusion but had normalized after 14 days. Elevated RCC or EPO levels were not predictive of an increase in hemoglobin. Postnatal HbFg/dL was higher in babies who had received transfusions. The authors conclude that blood transfusions depress erythropoiesis in infants with AOP and stimulate HbF synthesis but this effect is not sustained. Reticulocyte counts and erythropoietin levels are unhelpful in predicting recovery from AOP.


Subject(s)
Anemia, Neonatal/therapy , Blood Transfusion , Erythropoiesis , Anemia, Neonatal/blood , Erythropoietin/blood , Female , Fetal Hemoglobin/analysis , Humans , Infant, Newborn , Infant, Premature/blood , Male , Reticulocyte Count/methods
8.
Cochrane Database Syst Rev ; (2): CD004211, 2005 Apr 18.
Article in English | MEDLINE | ID: mdl-15846701

ABSTRACT

BACKGROUND: Clinical decision support systems (CDSS) are computer-based information systems used to integrate clinical and patient information to provide support for decision-making in patient care. They may be useful in aiding the diagnostic process, the generation of alerts and reminders, therapy critiquing/planning, information retrieval, and image recognition and interpretation. CDSS for use in adult patients have been evaluated using randomised control trials and their results analysed in systematic reviews. There is as yet no systematic review on CDSS use in neonatal medicine. OBJECTIVES: To examine whether the use of clinical decision support systems has an effect on 1. the mortality and morbidity of newborn infants and 2. the performance of physicians treating them SEARCH STRATEGY: The standard search method of the Cochrane Neonatal Review Group was used. Searches were made of the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, Issue 1, 2004), MEDLINE (from 1966 to August 2004), EMBASE (1980-2004), CINAHL (1982 to August 2004) and AMED (1985 to August 2004). SELECTION CRITERIA: Randomised or quasi-randomised controlled trials which compared the effects of CDSS versus no CDSS in the care of newborn infants. Trials which compared CDSS against other CDSS were also considered. The eligible interventions were CDSS for computerised physician order entry, computerised physiological monitoring, diagnostic systems and prognostic systems. DATA COLLECTION AND ANALYSIS: Studies were assessed for eligibility using a standard pro forma. Methodological quality was assessed independently by the different investigators. MAIN RESULTS: Two studies fitting the selection criteria were found for computer aided prescribing and one study for computer aided physiological monitoring.Computer-aided prescribing: one study (Cade 1997) examined the effects of computerised prescribing of parenteral nutrition ordering. No significant effects on short-term outcomes were found and longer term outcomes were not studied. The second study (Balaguer 2001) investigated the effects of a database program in aiding the calculation of neonatal drug dosages. It was found that the time taken for calculation was significantly reduced and there was a significant reduction in the number of calculation errors.Computer-aided physiological monitoring: one eligible study (Cunningham 1998) was found which examined the effects of computerised cot side physiological trend monitoring and display. There were no significant effects on mortality, volume of colloid infused, frequency of blood gases sampling (samples per day) or severe (Papile Grade 4) intraventricular haemorrhage. Published data did not permit us to analyse effects on long-term neurodevelopmental outcome. AUTHORS' CONCLUSIONS: There are very limited data from randomised trials on which to assess the effects of clinical decision support systems in neonatal care. Further evaluation of CDSS using randomised controlled trials is warranted.


Subject(s)
Decision Support Systems, Clinical , Perinatal Care/methods , Decision Making, Computer-Assisted , Drug Therapy, Computer-Assisted , Humans , Infant, Newborn , Monitoring, Physiologic/methods , Randomized Controlled Trials as Topic
9.
Acta Paediatr ; 91(3): 292-6, 2002.
Article in English | MEDLINE | ID: mdl-12022301

ABSTRACT

UNLABELLED: A randomized, controlled, prospective study of 80 preterm infants of birthweight less than 1750 g requiring ventilatory support was performed. While ventilatory support was required group TF (39 infants) received trophic feeding (0.5-1 ml h(-1)) along with parenteral nutrition, whereas group C (41 infants) received parenteral nutrition alone. When ventilatory support was no longer required milk feeds were started in group C and then increased in both groups until full milk feeds were established. The ratio of lactase to sucrase activity (L:S ratio) was measured in aspirated proximal intestinal fluid on 3 occasions: immediately after ventilatory support was withdrawn (T0), 7 days later (T7) and 14 days later (T14). On the same 3 occasions faecal chymotrypsin activity was measured. The mean difference (95% confidence interval) L:S ratio was significantly higher in group TF at both T0 and T14, 1.8 (0.03, 3.57) and 0.78 (0.2, 1.35) U l(-1), respectively. There was no significant difference in faecal chymotrypsin concentration. CONCLUSION: Trophic feeding alters relative intestinal disaccharidase activity, probably by inducing lactase production, but has no effect on pancreatic chymotrypsin activity.


Subject(s)
Chymotrypsin/metabolism , Digestive System/enzymology , Enteral Nutrition/methods , Infant, Premature/growth & development , Pancreas/enzymology , Parenteral Nutrition/methods , Chymotrypsin/analysis , Confidence Intervals , Feces/chemistry , Female , Follow-Up Studies , Humans , Infant, Low Birth Weight , Infant, Newborn , Lactase , Male , Probability , Prospective Studies , Respiration, Artificial , Statistics, Nonparametric , Sucrase/analysis , Sucrase/metabolism , beta-Galactosidase/analysis , beta-Galactosidase/metabolism
11.
Dev Med Child Neurol ; 43(4): 274-6, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11305406

ABSTRACT

We describe a term infant with an acute spinal cord injury following emergency Caesarean section. Foetal movements were normal on the day that the mother was admitted for postterm induction of labour. Caesarean section was performed because of foetal distress and failure to progress during labour. The initial clinical picture suggested acute birth asphyxia. The presence of a high cervical spine injury became more obvious as the clinical picture evolved over the next 7 days. A discontinuity of the cervical spinal cord at C4-5 was confirmed on MRI. Spontaneous respiration failed to develop and intensive care was withdrawn on day 15. No evidence of trauma, or a vascular, neurological, or congenital anomaly of the cervical spinal cord was found at post mortem. The absence of a similar case following cephalic presentation and Caesarean section made bereavement counselling of the parents especially difficult.


Subject(s)
Cesarean Section , Spinal Cord Injuries/etiology , Cervical Vertebrae/injuries , Fatal Outcome , Female , Humans , Infant, Newborn , Labor Presentation , Magnetic Resonance Imaging , Male , Pregnancy , Spinal Cord Injuries/pathology
12.
Arch Dis Child Fetal Neonatal Ed ; 84(2): F129-30, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11207231

ABSTRACT

AIM: To assess the value of contrast versus plain radiography in determining radio-opaque long line tip position in neonates. METHODS: In a prospective study, plain radiography was performed after insertion of radio-opaque long lines. If the line tip was not visible on the plain film, a second film with contrast was obtained in an attempt to visualise the tip. RESULTS: Sixty eight lines were inserted during the study period, 62 of which were included in the study. In 31, a second radiographic examination with contrast was necessary to determine position of the tip. In 29 of these, the line tip was clearly visualised with contrast. On two occasions, the line tip could not be seen because the contrast had filled the vein and obscured the tip from view. Eight of the lines that required a second radiograph with contrast were repositioned. CONCLUSION: Intravenous contrast should be routinely used in the assessment of long line position in the neonate.


Subject(s)
Catheterization, Central Venous/methods , Contrast Media , Radiography, Interventional/methods , Humans , Infant, Newborn , Observer Variation , Prospective Studies , Retreatment
13.
J Perinatol ; 21(7): 461-4, 2001.
Article in English | MEDLINE | ID: mdl-11894516

ABSTRACT

Fatal cardiac tamponade is a well recognised complication of the use of central venous catheters in neonatal patients. There is controversy over optimum catheter tip position to balance catheter performance against risk of adverse events. We report a series of five cases of tamponade occurring in one neonatal unit over a 4-year period, related to catheter tip placement in the right atrium. Right atrial catheter angulation, curvature or looping (CA) was present in all five cases on plain radiograph. It was frequently seen in other patients over the same period. Review of the literature indicates that CA was present in 6 of the 11 previous cases where the presence or absence of CA can be determined. Where right atrial catheter tip placement is accepted, clinicians should be aware of this characteristic catheter configuration, which is a major risk factor for cardiac tamponade. We recommend that catheter tips should not be placed in the right atrium to avoid risk of tamponade.


Subject(s)
Cardiac Tamponade/etiology , Catheterization, Central Venous/adverse effects , Catheters, Indwelling/adverse effects , Heart Atria/injuries , Cardiac Tamponade/mortality , Humans , Infant, Newborn , Risk Factors
14.
Arch Dis Child Fetal Neonatal Ed ; 82(3): F237-42, 2000 May.
Article in English | MEDLINE | ID: mdl-10794794

ABSTRACT

AIMS: To describe the relation between oscillatory amplitude changes and arterial blood gas (ABG) changes in preterm infants receiving high frequency oscillatory ventilation, using a multiparameter intra-arterial sensor (MPIAS). METHODS: Continuous MPIAS ABG data were collected after amplitude changes and stratified according to FIO(2): high (> 0.4) or low (< 0.3). For each amplitude change, the maximum change (from baseline) in PaCO(2) and PaO(2) over the following 30 minutes was determined. In total, 64 oscillatory amplitude changes were measured in 21 infants (median birth weight 1040 g; gestation 27 weeks). RESULTS: All amplitude increases produced PaCO(2) falls (median -0.98 and -1.13 kPa for high and low FIO(2) groups respectively). All amplitude decreases produced PaCO(2) rises (median +0.94 and +1.24 kPa for high and low FIO(2) groups respectively). About 95% of the change in PaCO(2) was completed in 30 minutes. Amplitude changes did not affect PaO(2) when FIO(2) > 0.4. When FIO(2) < 0.3, amplitude increases produced a PaO(2) rise (median = +1.1 kPa; P < 0.001) and amplitude decreases a fall (median = -1.2 kPa; P < 0.001). CONCLUSIONS: After oscillatory amplitude changes, the speed but not the magnitude of the PaCO(2) change is predictable, and a rapid PaO(2) change accompanies the PaCO(2) change in infants with mild lung disease and a low FIO(2).


Subject(s)
Carbon Dioxide/blood , High-Frequency Ventilation/methods , Infant, Premature/blood , Lung Diseases/blood , Oxygen/blood , Blood Gas Analysis , Humans , Infant, Newborn , Lung Diseases/therapy , Oscillometry/adverse effects , Partial Pressure , Tidal Volume/physiology , Time Factors
15.
Clin Perinatol ; 27(1): 221-34, viii, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10690573

ABSTRACT

Clinical practice demands knowledge of gastrointestinal ontogeny and the factors that affect our ability to use enteral feeding in the micropremie. The decisions regarding milk type (when and how it should be given) are considered in the light of current physiologic and clinical evidence. Special considerations apply in the micropremie who is also small for gestational age and NEC must be avoided. Trophic feeding now has an established role, allowing the infant to benefit from enteral feeds even when full nutritive milk feeding is not possible.


Subject(s)
Enteral Nutrition , Infant Nutritional Physiological Phenomena , Infant, Premature , Infant, Very Low Birth Weight , Adult , Enteral Nutrition/methods , Gastrointestinal Motility/physiology , Humans , Infant, Newborn , Infant, Premature/physiology , Infant, Very Low Birth Weight/physiology , Milk, Human
16.
Arch Dis Child Fetal Neonatal Ed ; 82(1): F29-33, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10634838

ABSTRACT

AIMS: To determine the effect of trophic feeding on clinical outcome in ill preterm infants. METHODS: A randomised, controlled, prospective study of 100 preterm infants, weighing less than 1750 g at birth and requiring ventilatory support and parenteral nutrition, was performed. Group TF (48 infants) received trophic feeding from day 3 (0.5-1 ml/h) along with parenteral nutrition until ventilatory support finished. Group C (52 infants) received parenteral nutrition alone. "Nutritive" milk feeding was then introduced to both groups. Clinical outcomes measured included total energy intake and growth over the first six postnatal weeks, sepsis incidence, liver function, milk tolerance, duration of respiratory support, duration of hospital stay and complication incidence. RESULTS: Groups were well matched for birthweight, gestation and CRIB scores. Infants in group TF had significantly greater energy intake, mean difference 41.4 (95% confidence interval 9, 73.7) kcal/kg p=0.02; weight gain, 130 (CI 1, 250) g p = 0.02; head circumference gain, mean difference 0.7 (CI 0.1, 1.3) cm, p = 0.04; fewer episodes of culture confirmed sepsis, mean difference -0.7 (-1.3, -0.2) episodes, p = 0.04; less parenteral nutrition, mean difference -11.5 (CI -20, -3) days, p = 0. 03; tolerated full milk feeds (165 ml/kg/day) earlier, mean difference -11.2 (CI -19, -3) days, p = 0.03; reduced requirement for supplemental oxygen, mean difference -22.4 (CI-41.5, -3.3) days, p = 0.02; and were discharged home earlier, mean difference -22.1 (CI -42.1, -2.2) days, p = 0.04. There was no significant difference in the relative risk of any complication. CONCLUSIONS: Trophic feeding improves clinical outcome in ill preterm infants requiring parenteral nutrition.


Subject(s)
Enteral Nutrition/methods , Infant, Premature, Diseases , Infant, Premature , Animals , Confidence Intervals , Energy Intake , Female , Hospitalization , Humans , Incidence , Infant Nutritional Physiological Phenomena , Infant, Low Birth Weight , Infant, Newborn , Infant, Premature/growth & development , Infant, Premature, Diseases/etiology , Infant, Premature, Diseases/physiopathology , Length of Stay , Liver/physiology , Male , Milk , Milk, Human , Parenteral Nutrition , Prospective Studies , Respiration, Artificial , Sepsis/etiology , Time Factors , Treatment Outcome
17.
J R Coll Surg Edinb ; 45(6): 411-4, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11153436

ABSTRACT

Solitary rectal ulcer syndrome (SRUS) is rare in children. Few reported cases have undergone detailed investigations, treatments have been extremely varied and outcome poorly documented. We report two cases of SRUS in children, each with a different macroscopic pathology. The diagnosis was delayed in both cases. The importance of appropriate investigation and the need to tailor treatment to the type of lesion are emphasised. One case of SRUS was associated with a complete, full thickness rectal prolapse and symptoms improved after an abdominal sutured rectopexy. The other patient responded well to endoanal excision of polypoid lesions. The diagnosis and management of this condition in children deserves wider recognition.


Subject(s)
Rectal Diseases/diagnosis , Ulcer/diagnosis , Adolescent , Child , Colonic Polyps/complications , Colonic Polyps/surgery , Diagnosis, Differential , Humans , Male , Rectal Diseases/surgery , Rectal Prolapse/complications , Rectal Prolapse/surgery , Ulcer/complications , Ulcer/surgery
18.
Pediatrics ; 104(6): e76, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10586010

ABSTRACT

OBJECTIVE: Published data show that plasma creatinine falls steadily during the first 28 days of life and that creatinine levels in the neonatal period are higher in more premature infants. However, the best reference data commence on day 2 of life. The objective of this study was to document how plasma creatinine changes in the first 48 hours of life and to examine the reason for the apparently high levels of creatinine in preterm infants, compared with maternal levels. DESIGN: A prospective observational study on a regional neonatal intensive care unit. PATIENTS: A total of 42 preterm infants, mean gestational age of 29.4 weeks (range: 23-35), mean birth weight of 1.42 kg (.55-2.77), divided into 4 gestation groups: 23 to 26 weeks (n = 9), 27 to 29 weeks (n = 13), 30 to 32 weeks (n = 12), and 33 to 35 weeks (n = 8). INTERVENTIONS: Measurement of plasma creatinine and urea concentration in cord blood and in serial samples taken for routine arterial blood gas analysis. OUTCOME MEASUREMENTS: Changes in creatinine concentration with time and relationship to gestational age, birth weight, and illness severity. RESULTS: Mean creatinine at birth was 73 micromol/L (95% confidence interval [CI]: 68-79 micromol/L). Plasma creatinine rose significantly over the first 48 hours. Mean peak creatinine in the most preterm infants (23-26 weeks) was 221 micromol/L (CI: 195-247 micromol/L). Peak plasma creatinine was inversely related to gestation (Spearman's coefficient: -.73) and birth weight (Spearman's coefficient: -.76). Significant differences in creatinine concentration were seen among different gestational groups at 24 and 48 hours of life. Peak creatinine correlated with a high Clinical Risk Index for Babies score (Spearman's coefficient:. 64). The fall in creatinine began later in more premature infants. All 38 surviving infants had normal renal function; their mean plasma creatinine at discharge was 52 micromol/L (CI: 46-58 micromol/L). CONCLUSIONS: Rather than falling steadily from birth, creatinine rises dramatically in the first 48 hours of life, especially in infants of <30 weeks' gestation. Even large rises in creatinine in the first 48 hours may be expected and should not be used in isolation to diagnose renal failure.


Subject(s)
Creatinine/blood , Infant, Premature/blood , Birth Weight , Fetal Blood/chemistry , Gestational Age , Humans , Infant, Newborn , Infant, Premature, Diseases/blood , Prospective Studies , Severity of Illness Index , Urea/blood
20.
Arch Dis Child Fetal Neonatal Ed ; 80(2): F93-8, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10325783

ABSTRACT

AIMS: To compare arterial blood gas (ABG) readings obtained with a multiparameter intra-arterial sensor with those from an ABG analyser. METHODS: An MPIAS with the ability to measure continuously pH, PaCO2, and PaO2 was introduced via an umbilical arterial catheter in 27 neonates requiring intensive care. They underwent 3260 hours of MPIAS monitoring, during which 753 ABG readings were performed. RESULTS: Overall bias (mean difference: MPIAS-ABG) and precision (standard deviation of differences) values were: -0.002 and 0.022, respectively, for pH; +0.26 and 0.52 for PaCO2 (kPa); and -0.19 and 0.99 for PaO2 (kPa). This gave 95% limits of agreement as: -0.047 to +0.042 for pH, -0.76 to +1.28 kPa for PaCO2, and -2.13 to +1.75 kDa for PaO2. For each variable, precision across readings from the same individual was better than overall precision for all data. No complications related to the use of the catheter were observed. CONCLUSIONS: Continuous MPIAS ABG monitoring is an exciting development, with the potential to reduce blood transfusions and improve ABG homeostasis.


Subject(s)
Blood Gas Analysis/instrumentation , Infant, Premature/blood , Monitoring, Physiologic/instrumentation , Carbon Dioxide/blood , Female , Humans , Hydrogen-Ion Concentration , Infant, Newborn , Intensive Care, Neonatal , Male , Oxygen/blood , Sensitivity and Specificity
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