Sunday, December 21, 2014

Correlation Between Serum Caffeine Levels And Outcomes in Preterm Infants.

http://www.nature.com/jp/journal/vaop/ncurrent/full/jp2014226a.html

Serum caffeine concentrations and short-term outcomes in premature infants of 29 weeks of gestation

P Alur, V Bollampalli, T Bell, N Hussain and J Liss
Abstract

Objective:


Caffeine is effective in the treatment of apnea of prematurity but it is not well known if the therapeutic concentration of the drug has an impact on other neonatal outcomes such as chronic lung disease (CLD). The aim of this study was to determine if there is an association between caffeine concentrations and the incidence of CLD in premature infants of 29 weeks of gestation.
Study design:
A retrospective chart review of all the infants born 29 weeks of gestation from 2007 to 2011, who survived until discharge or 36 weeks postmenstrual age, was conducted. Caffeine concentrations were obtained weekly on infants getting the drug. Average caffeine concentrations (ACCs) were determined for the duration of caffeine therapy and correlated with CLD, length of stay (LOS), oxygen at discharge (OD), duration of ventilation (DV) and total charges for hospitalization for each patient.


Results:

Of the 222 eligible infants, 198 met the inclusion criteria. ACC for infants without CLD was 17.0±3.8 μg ml−1 compared with infants with CLD 14.3±6.1 μg ml−1 (P<0.001). Infants receiving high ACC (>14.5 μg ml−1) had lower incidence of patent ductus arteriosus, lesser number of days on ventilator and oxygen, lesser need for diuretics, lower incidence of CLD, were more likely to go home without supplemental OD and had lower LOS and lower total hospital charges (all differences were significant P<0.05) Multiple logistic regression modeling after adjusting for confounding variables indicated that higher caffeine concentrations were significantly associated with decrease in CLD. Receiver operating curve analysis confirmed a significant predictive ability of caffeine concentration for CLD with a cutoff concentration of 14.5 μg ml−1 (sensitivity of 42.6 and specificity of 86.8). The AUC (area under the curve) for the prediction of CLD was 0.632 (95% confidence interval 0.56–0.69, P=0.009). Conclusions:

Caffeine concentrations >14.5 μg ml−1 were strongly correlated with reduced CLD in infants born at 29 weeks of gestation. Higher caffeine concentrations were associated with decreased total hospital charges, DV, OD and LOS. Additional randomized trials are needed to confirm these findings, to identify ideal serum concentrations and determine possible long-term neurologic benefits.

Thursday, December 4, 2014

Umbilical Cord Milking-Evidence in Preterm Infants

http://archpedi.jamanetwork.com/article.aspx?articleID=1919654#Abstract


JAMA Pediatr. 2014 Nov 3. doi: 10.1001/jamapediatrics.2014.1906. [Epub ahead of print]
Efficacy and Safety of Umbilical Cord Milking at Birth: A Systematic Review and Meta-analysis.
Al-Wassia H1, Shah PS2.


Author information

1Department of Pediatrics, King Abdulaziz University, Jeddah, Saudi Arabia.
2Department of Pediatrics, Mt Sinai Hospital, Toronto, Ontario, Canada3Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada.



Abstract



Importance:


Umbilical cord milking (UCM) is suggested to improve neonatal outcomes.
Objectives:


To perform a systematic review and meta-analysis of the efficacy and safety of UCM in full-term and preterm neonates.
Data Sources:


A systematic search of MEDLINE, EMBASE, CINAHL, the Cochrane Database of Clinical Trials, the clinicaltrails.gov database, and the reference list of retrieved articles from 1940 to 2014.
Study Selection:


Randomized clinical trials comparing UCM with other strategies of handling the umbilical cord at birth in full-term and preterm infants. Seven of the 18 initially identified studies were selected.
Data Extraction and Synthesis:


Two reviewers independently extracted data and assessed the risk for bias in included trials using the criteria outlined in the Cochrane Handbook for Systematic Reviews of Interventions.
Main Outcomes and Measures:


Neonatal mortality before discharge from the hospital.
Results:


We included 7 randomized clinical trials involving 501 infants. Infants with a gestational age of less than 33 weeks allocated to UCM compared with control conditions showed no difference in the risk for mortality (risk ratio [RR], 0.75 [95% CI, 0.35 to 1.64]; risk difference [RD], -0.02 [95% CI, -0.09 to 0.04]), hypotension requiring volume expanders (RR, 0.71 [95% CI, 0.41 to 1.25]; RD, -0.09 [95% CI, -0.22 to 0.05]), or inotrope support (RR, 0.77 [95% CI, 0.51 to 1.17]; RD, -0.10 [95% CI, -0.25 to 0.05]). Higher initial levels of hemoglobin (mean difference, 2.0 [95% CI, 1.3-2.7] g/dL) and hematocrit (mean difference, 4.5% [95% CI, 1.5%-7.4%]) were identified in the UCM groups.
We found a reduced risk for oxygen requirement at 36 weeks (RR, 0.42 [95% CI, 0.21 to 0.83]; RD, -0.14 [95% CI, -0.25 to -0.04]) and for intraventricular hemorrhage of all grades (RR, 0.62 [95% CI, 0.41 to 0.93]; RD, -0.12 [95% CI, -0.22 to -0.02]) in infants assigned to UCM. Among infants with a gestational age of at least 33 weeks, UCM was associated with higher hemoglobin levels in the first 48 hours in 224 infants (mean difference, 1.2 [95% CI, 0.8-1.5] g/dL) and at 6 weeks of life in 170 infants (mean difference, 1.1 [95% CI, 0.7-1.5] g/dL).
Conclusions and Relevance:


Umbilical cord milking was associated with some benefits and no adverse effects in the immediate postnatal period in preterm infants gestational age, <33 nbsp="" p="" weeks.="">

 

 
 



Saturday, November 1, 2014

Neonatal Survival After Prolonged Preterm Premature Rupture of Membranes Before 24 Weeks of Gestation

Obstetrics & Gynecology:
       
Brumbaugh, Jane E. MD; Colaizy, Tarah T. MD, MPH; Nuangchamnong, Nina MD; O'Brien, Emily A.; Fleener, Diedre K. RN, BSN; Rijhsinghani, Asha MD; Klein, Jonathan M. MD
Abstract
OBJECTIVE: To evaluate neonatal survival after prolonged preterm premature rupture of membranes (PROM) in the era of antenatal corticosteroids, surfactant, and inhaled nitric oxide.
METHODS: A single-center retrospective cohort study of neonates born from 2002–2011 after prolonged (1 week or more) preterm (less than 24 weeks of gestation) rupture of membranes was performed. The primary outcome was survival to discharge. Neonates whose membranes ruptured less than 24 hours before delivery (n=116) were matched (2:1) on gestational age at birth, sex, and antenatal corticosteroid exposure with neonates whose membranes ruptured 1 week or more before delivery (n=58). Analysis used conditional logistic regression for categorical data and Wilcoxon signed rank test for continuous data.
RESULTS: The prolonged preterm PROM exposed and unexposed cohorts had survival rates of 90% and 95%, respectively, although underpowered to assess the statistical significance (P=.313). Exposed neonates were more likely have pulmonary hypoplasia (26/58 exposed, 1/114 unexposed, P<.001), pulmonary hypertension (21/56 exposed, 10/112 unexposed, P<.001), and pulmonary air leak (21/58 exposed, 14/114 unexposed, P<.001). Gestational age at rupture (20.4 weeks exposed, 22.3 weeks unexposed, P=.189), length of rupture (3.7 weeks exposed, 6.4 weeks unexposed, P=.717), and lowest maximal vertical pocket before 24 weeks of gestation (0 cm exposed, 1.4 cm unexposed, P=.114) did not discriminate between survivors and nonsurvivors after exposure to prolonged preterm PROM.
CONCLUSION: With antenatal steroid exposure and aggressive pulmonary management, survival to discharge after prolonged preterm PROM was 90%. Pulmonary morbidities were common. Of note, the data were limited to women who remained pregnant 1 week or longer after rupture of membranes.

Saturday, October 4, 2014

A Theme Park In The Midair!


A Mid Air Theme Park

 

It was time to revel in the wedding festivities again. As my niece was getting married, we were excited and began to look for competitive airfares to India. This newer airlines, with which we had no previous experience, had an enticing pricing. Nothing else mattered, except the tickets for the three. They even offered exit row seats just for your bi-weekly paycheck! A deal we couldn’t refuse, as we were eager to be fresh when we arrived after 20 hours of flight time.

The check-in was a breeze, and the security did not displease. As we placed our luggage in the overhead bins, we began to settle in our ordained seats. Am I adipose? No airlines has ever made me feel this way I suppose! I began to doubt my body frame and my BMI of 22? Is it the slice of pizza I ate a month ago causing this? Or may be it was my Scott Evest, I thought filled with gadgets. I took off the evest. Yet, the same feeling persisted. I may have to take off my pants to fit in snuggly! Though, it was desirable, but may be unbearable for others. It was a level four pushup exercise to free yourself from the skin-tight seat. My arms were stronger by the end of the journey. These seats seemed to compensate for seat belt non-compliance, I thought.

I have seen many companies vying for movie theme toys to please their customers. However, this airlines went up a notch and incorporated a movie theme to entertain their passengers. After waiting, which seemed long like an uncut Benhur movie, I finally got a chance to use the toilet. I quickly realized that you have to be a Spider Man to accomplish the purpose of your visit. The whole floor was wet. It was difficult to discern if it was the result of aimless target practice of the previous human or just plain water. I just couldn’t take the chance. I had to take the support of the faucet and the side wall, and raise myself with my already stronger arms (now I understood why they made seats as tiny they are) and place my feet on the side panels, and balance myself and execute the job with utmost precision. I profusely thanked the airlines for such a personable experience. May be people should carry long poles to walk on in to this spider man theme park in midair!

A stride back to my seat was no solace either. The guy behind my seat kept tapping my seat hysterically to the extent that I had to turn back and ask him if he needed my attention. He felt ashamed to have woken up a Spiderman! I have heard of interactive movies, but never really comprehended. The tiny smudged tv screen in the front provided such an unique experience. When you choose a movie after several taps, it begins with an advertisement. The movie begins and freezes. You had to tap the screen several times to restart the movie. It kept me busy to interact with the screen to keep the movie going. It is possible that my ashamed co-passenger might have had a mature scene freeze with his son ogling at it leading to his frantic banging on the screen to wake up this freshly trained Spiderman.

As I was attempting another peaceful nap, a flight attendant came to ask me if I needed something to drink. I was not sure what the Spiderman drank normally. After a prolonged ponder, I asked for a mango juice and water. She confirmed that I wanted “wother”. I affirmed and said “water”. She reaffirmed and said she would get me “mongo and VOTHER”. I was at a loss, but appreciated. She came back promptly after half an hour with a glass of juice, which looked like mango juice. There was no glass of water. Hoping that she would bring it later, I sipped the MONGO juice imposter. It was very bitter and disgusting. I immediately asked her, if the juice was spoiled and fermented as it was very bitter. Then she said it may be due to WOTHkER. I was confused as I heard a different pronunciation each time. She then showed me the VODKA (Wother or Wothker), which I believe she decided I wanted it sub consciously. She went above and beyond her call of duty (probably the airline motto!), and decided to serve him more than he asked for. I am a congenital teetotaler and this lady wanted to give it a damn break.  I had to purify myself. I had no other choice but to visit the only theme park with unlimited number of free passes.

Monday, July 28, 2014

Revised 2014 Guidelines for RSV Prphylaxis

http://aapnews.aappublications.org/content/35/8/1.1.full

In the first year of life, palivizumab prophylaxis is recommended for infants born before 29 weeks, 0 days’ gestation.
  • Palivizumab prophylaxis is not recommended for otherwise healthy infants born at or after 29 weeks, 0 days’ gestation.
    • Previously, prophylaxis was recommended for preterm infants born before 32 weeks’ gestation. Infants with certain risk factors born at 32 weeks, 0 days to 34 weeks, 6 days also were eligible.
  • In the first year of life, palivizumab prophylaxis is recommended for preterm infants born before 32 weeks, 0 days’ gestation with chronic lung disease of prematurity defined as greater than 21% oxygen for at least 28 days after birth.
    • Previously, no definition of chronic lung disease was provided.
  • Clinicians may administer palivizumab prophylaxis in the first year of life to certain infants with hemodynamically significant heart disease. In addition, consultation with a cardiologist for decisions about prophylaxis is recommended for patients with cyanotic heart disease.
    • Previously, prophylaxis also was recommended in the second year of life for certain infants with hemodynamically significant heart disease.
  • Clinicians may administer up to a maximum of five monthly doses of palivizumab during the RSV season to infants who qualify for prophylaxis in the first year of life (including those in Florida). Qualifying infants born during the RSV season will require fewer doses. For example, infants born in January would receive their last dose in March.
    • Previously, fewer than five monthly doses were recommended for some infants.
  • Palivizumab prophylaxis is not recommended in the second year of life except for children who require at least 28 days of supplemental oxygen after birth and who continue to require medical intervention (supplemental oxygen, chronic corticosteroid or diuretic therapy).
    • Previously, two seasons of prophylaxis were recommended.
  • Monthly prophylaxis should be discontinued in any child who experiences a breakthrough RSV hospitalization.
    • Previously, continued prophylaxis was recommended in a child who experienced a breakthrough RSV hospitalization.
  • Children with pulmonary abnormality or neuromuscular disease that impairs the ability to clear secretions from the lower airways may be considered for prophylaxis in the first year of life.
    • Previous recommendation was for two years of prophylaxis.
  • Children younger than 24 months of age who will be profoundly immunocompromised during the RSV season may be considered for prophylaxis.
    • Similar to previous recommendation.
  • Insufficient data are available to recommend palivizumab prophylaxis routinely for children with cystic fibrosis or Down syndrome.
    • Previously, the recommendation for children with cystic fibrosis was similar; children with Down syndrome were not addressed.
  • The burden of RSV disease in certain remote areas may result in a broader use of palivizumab for RSV prevention in Alaska Native populations and possibly in other selected Native American populations.
    • Present recommendations allow for greater flexibility for Alaska Native and Native American populations.
  • Palivizumab prophylaxis is not recommended for prevention of RSV nosocomial disease.

  • Monday, May 26, 2014

    A Risk of Sensory Deprivation in the Neonatal Intensive Care Unit

    http://www.jpeds.com/article/S0022-3476(14)00112-7/fulltext
    Alan. H. Jobe.

    Sound Exposures in NICU:
    ...........The appropriate emphasis on sound abatement in the new or renovated NICU should be on background noise, alarm noise, and other non-human noises that can startle and disrupt sleep of the preterm.13 However, the focus on noise abatement has morphed into a goal of silence in the NICU with exclusion of staff talk and lively discussions on work rounds. The result may be a severe limitation of the exposure of the vulnerable developing auditory cortex to human voices and sounds that are necessary for language development. This delay in language development for infants in single rooms is just what was observed by the Pineda article.3 In contrast, the open ward better reflects the fetal environment with human sounds and activities.

    Light Exposures in NICU:
    ......... Circadian rhythms regulate more than sleep cycles, and there is minimal research to explore other potential effects of light on the preterm infant. Accepting that the fetus has a circadian rhythm and the dark-exposed preterm infant does not, the conservative approach to exposure of the preterm infant to light would be cycling of dim light sufficient for care at night to brighter light during the day. The covering of the isolettes with blankets continuously seems to be questionable because visual development requires light exposure. The biology suggests that judicious light exposure is appropriate until more is known about the effects of light on the preterm infant.

    Tracheostomies in preterm infants associated with higher morbidities?

    http://www.jpeds.com/article/S0022-3476(13)01560-6/abstract

    Objectives

    To evaluate the neurodevelopmental outcomes of very preterm (<30 infants="" p="" tracheostomy.="" underwent="" weeks="" who="">

    Study design

    Retrospective cohort study from 16 centers of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network over 10 years (2001-2011). Infants who survived to at least 36 weeks (N = 8683), including 304 infants with tracheostomies, were studied. Primary outcome was death or neurodevelopmental impairment (NDI; a composite of ≥1 of developmental delay, neurologic impairment, profound hearing loss, severe visual impairment) at a corrected age of 18-22 months. Outcomes were compared using multiple logistic regression. We assessed the impact of timing by comparing outcomes of infants who underwent tracheostomy before and after 120 days of life.

    Results

    Tracheostomies were associated with all neonatal morbidities examined and with most adverse neurodevelopmental outcomes. Death or NDI occurred in 83% of infants with tracheostomies and 40% of those without (OR adjusted for center 7.0, 95% CI 5.2-9.5). After adjustment for potential confounders, odds of death or NDI remained higher (OR 3.3, 95% CI 2.4-4.6), but odds of death alone were lower (OR 0.4, 95% CI 0.3-0.7) among infants with tracheostomies. Death or NDI was lower in infants who received their tracheostomies before, rather than after, 120 days of life (aOR 0.5, 95% CI 0.3-0.9).

    Conclusions

    Tracheostomy in preterm infants is associated with adverse developmental outcomes and cannot mitigate the significant risk associated with many complications of prematurity. These data may inform counseling about tracheostomy in this vulnerable population.

    Sunday, May 11, 2014

    Musings of A MedMan: Oh Mother! What is Thy Nature?

    Musings of A MedMan: Oh Mother! What is Thy Nature?:   Oh our dear Mother You are the Nature’s Best For He created you, so He could Rest. By nature, you shower endless kindness T...

    Saturday, May 10, 2014

    Oh Mother! What is Thy Nature?

     

    Oh our dear Mother

    You are the Nature’s Best

    For He created you, so He could Rest.

    By nature, you shower endless kindness

    Through nurture, we taste your tenderness.

    Drowned in the flood of your love, we are reminded of Nature’s force

    Oh Mother!

    Respecting you is respecting our Mother Nature

     For the Mother Nature, you are her human form.

    Like trees with delicious peach,

    You provide us delicious food moment we reach

    Like the sun, and soft breeze

    You are the light of our lives

     Gently caressing our painful Hives.

    Our jabs and jeers, you take with a cheer.

    To give love is thy nature-A Mother(’s) Nature.

     

    Pradeep Alur.

     

     

    Friday, April 4, 2014

    Low Pre-Transfusion Hematocrit May Predispose to NEC!

    http://www.earlyhumandevelopment.com/article/S0378-3782(14)00047-4/abstract

    Feeding practices and other risk factors for developing transfusion-associated necrotizing entrocolitis.

    Aims
    The objective of this study is to determine the incidence of and risk factors for necrotizing enterocolitis (NEC) and transfusion-associated NEC (TANEC) in very-low-birth-weight (VLBW) infants pre/post implementation of a peri-transfusion feeding protocol.

    Study design

    A retrospective cohort study was conducted including all inborn VLBW infants admitted to the Duke intensive care nursery from 2002 to 2010. We defined NEC using Bell's modified criteria IIA and higher and TANEC as NEC occurring within 48hours of a packed red blood cell (pRBC) transfusion. We compared demographic and laboratory data for TANEC vs. other NEC infants and the incidence of TANEC pre/post implementation of our peri-transfusion feeding protocol. We also assessed the relationship between pre-transfusion hematocrit and pRBC unit age with TANEC.

    Results

    A total of 148/1380 (10.7%) infants developed NEC. Incidence of NEC decreased after initiating our peri-transfusion feeding protocol: 126/939 (12%) to 22/293 (7%), P=0.01. The proportion of TANEC did not change: 51/126 (41%) vs. 9/22 (41%), Pmore than 0.99. TANEC infants were smaller, more likely to develop surgical NEC, and had lower mean pre-transfusion hematocrits prior to their TANEC transfusions compared with all other transfusions before their NEC episode: 28% vs. 33%, P less than 0.001. Risk of TANEC was inversely related to pre-transfusion hematocrit: odds ratio 0.87 (0.79–0.95).

    Conclusions

    Pre-transfusion hematocrit is inversely related to risk of TANEC, which suggests that temporally maintaining a higher baseline hemoglobin in infants most at risk of NEC may be protective. The lack of difference in TANEC pre-/post-implementation of our peri-transfusion feeding protocol, despite an overall temporal decrease in NEC, suggests that other unmeasured interventions may account for the observed decreased incidence of NEC.

    Thursday, March 20, 2014

    Effects of Early Inhaled Nitric Oxide Therapy and Vitamin A Supplementation on the Risk for Bronchopulmonary Dysplasia in Premature Newborns with Respiratory Failure

    http://www.jpeds.com/article/S0022-3476%2813%2901475-3/abstract?elsca1=etoc&elsca2=email&elsca3=0022-3476_201404_164_4&elsca4=pediatrics

    Objective

    To assess whether the combination of early inhaled nitric oxide (iNO) therapy and vitamin A supplementation lowers the incidence of bronchopulmonary dysplasia (BPD) in premature newborns with respiratory failure.

    Study design

    A total of 793 mechanically ventilated infants (birth weight 500-1250 g) were randomized (after stratification by birth weight) to receive placebo or iNO (5 ppm) for 21 days or until extubation (500-749, 750-999, or 1000-1250 g). A total of 398 newborns received iNO, and of these, 118 (30%) received vitamin A according to their enrollment center. We compared patients who received iNO + vitamin A with those who received iNO alone. The primary outcome was a composite of death or BPD at 36 weeks postconceptual age.

    Results

    BPD was reduced in infants who received iNO + vitamin A for the 750-999 g birth weight group compared with iNO alone (P = .01). This group also showed a reduction in the combined outcome of BPD + death compared with iNO alone (P = .01). The use of vitamin A did not change the risk for BPD in the placebo group. Overall, the use of vitamin A was low (229 of 793 patients, or 29%). Combined therapy improved Bayley Scales of Infant Development II Mental and Psychomotor Developmental Index scores at 1 year compared with infants treated solely with iNO for the 500-749 g birth weight group.

    Conclusions

    In this retrospective analysis of the nonrandomized use of vitamin A, combined iNO + vitamin A therapy in preterm infants with birth weight 750-999 g reduced the incidence of BPD and BPD + death and improved neurocognitive outcomes at 1 year in the 500-749 g birth weight group.

    Association between Postnatal Dexamethasone for Treatment of Bronchopulmonary Dysplasia and Brain Volumes at Adolescence in Infants Born Very Preterm


    http://www.jpeds.com/article/S0022-3476(13)01379-6/abstract
  • Jeanie L.Y. Cheong, MD et.al

  • Objectives

    To compare brain volumes in adolescents who were born extremely preterm (<28 a="" and="" brain="" determine="" dexamethasone="" dose="" effect="" gestation="" had="" if="" on="" p="" postnatal="" received="" response="" there="" to="" volumes.="" was="" weeks="" who="">

    Study design

    Geographical cohort study of extremely preterm adolescents born in 1991-1992 in Victoria, Australia. T1-weighted magnetic resonance imaging was performed at 18 years of age. Segmented and parcellated brain volumes were calculated using an automated segmentation method (FreeSurfer) and compared between groups, with and without adjustment for potential confounders. The relationships between total postnatal dexamethasone dose and brain volumes were explored using linear regression.

    Results

    Of the 148 extremely preterm participants, 55 (37%) had received postnatal dexamethasone, with a cumulative mean dose of 7.7 mg/kg. Compared with participants who did not receive postnatal dexamethasone, those who did had smaller total brain tissue volumes (mean difference −3.6%, 95% CI [−7.0%, −0.3%], P value = .04) and smaller white matter, thalami, and basal ganglia volumes (all P < .05). There was a trend of smaller total brain and white matter volumes with increasing dose of postnatal dexamethasone (regression coefficient −7.7 [95% CI −16.2, 0.8] and −3.2 [−6.6, 0.2], respectively).

    Conclusions

    Extremely preterm adolescents who received postnatal dexamethasone in the newborn period had smaller total brain tissue volumes than those who did not receive postnatal dexamethasone, particularly white matter, thalami, and basal ganglia. Vulnerability of brain tissues or structures associated with postnatal dexamethasone varies by structure and persists into adolescence.

    Tuesday, February 25, 2014

    ACE inhibitors-Are they safe in newborns?

    http://link.springer.com/article/10.1007%2Fs00246-013-0813-2
    Pediatric Cardiology , Volume 35, Issue 3, pp 499-506

    The age range of neonates at ACEi initiation was 15.9–18.1 days. The inclusion criteria was met by 206 neonates: 168 term (82 %) and 38 preterm (18 %) newborns. The mean dose of captopril was 0.07 ± 0.009 mg/kg for the preterm neonates and 0.13 ± 0.019 mg/kg for the term neonates.

    Nearly 42 % of all the patients showed renal risk, with approximately 30 % demonstrating renal failure by modified pRIFLE (pediatric risk, injury, failure, loss, and end-stage renal disease) criteria. Despite the lack of significantly different CrCl, the premature neonates were more likely to experience ACEi-related renal failure by pRIFLE (55 %) than their term counterparts (23 %; p < 0.001). Despite its common use for term neonates with cardiac disease, ACEi should be used cautiously and only when indications are clear. These results also raise the question whether ACEi should be used at all for preterm neonates.

    Sunday, February 16, 2014

    Closed Captioning-Altered Version.


    Closed Caption.

    It was a busy day; rather a chaotic day! Nothing seemed to go smoothly that day. The situation was wearing down the mortals swiftly. The high acuity in the unit was leading to paucity of patience.

    As I was seriously contemplating, a colleague cozily meandered towards me. As she bent down towards my ear, I had an eerie feeling that she would literally bite my ear off. Such was the prevailing perception. She gently whispered in to my eager ears. It was Valentine’s Day! The whisper lingered just too long for a simple “we all love you”. A smile flashed on my mulling face, as I peeked at the distraught laced face. Smile, when you don’t understand was my philosophy, as it addresses 90% of the situations without repercussions.

    In the midst of mess and distress, as I pose to be in less stress, and hence, not anticipating a better response, she ambled away. I noticed in the meantime, alarms denoting serious problem going off. I rushed to the baby’s bed side to assess and make appropriate changes.  The at-risk seemed at-best now. I discussed and dispersed from the bedside.

    The whisperer strode to my chair huffing and puffing. “You can’t keep secrets can you?”- She looked irked and piqued. Surprise surfaced on my stoic face. I never heard any secrets, except for non-specific valentine wishes from her; that was what at least I thought she did! Hence, my dumb smile! I paused to ponder. “Secrets, which one?” I inquired. “Forget it!”, whisperer was visibly upset and marched away. I slowly walked towards her, and confessed my ignorance about her distress. “If I confide in you about an annoying colleague, you just don’t have to divulge it to her in such a swift manner” she burst out. I pointed towards my ear and confessed “don’t tell me secrets, not because I can’t keep them, but because I can’t hear them”. She then noticed the lack of aids of hearing and laughed out loudly.

    Later, I was at a party. It was dim and had din. I was jiving to a lilting tune with my better half. A well-dressed man walked up to me and whispered. I laughed and said “you are right” concurring with him instantly about the peppy song. My laughter was cut short, when my wife answered him “his name is P…….”. Obviously, agreeing with something you don’t understand could be unseemly upsetting. If you whisper, I cannot decipher. If you still choose to do so, I need closed captioning from someone!

    Wednesday, February 12, 2014

    Probiotics-Prime Time For Routine Use!

    http://www.jpeds.com/article/S0022-3476(13)01596-5/fulltext
    ProPrems trial is very compelling as 95% of the study participants received breast milk!


    Probiotic supplementation in preterm infants is perhaps the best studied yet least used therapy in neonatal medicine.1, 2 All recently published meta-analyses have reported significant impacts on important clinical outcomes.3, 4, 5 In the updated Cochrane meta-analysis,3 which includes 24 trials, there is a significant decrease in necrotizing enterocolitis (NEC) (relative risk [RR] 0.43, 95% CI 0.33-0.56; risk difference [RD] −0.03, 95% CI −0.04 to −0.02; P < .00001) and all-cause mortality (RR 0.65, 95% CI 0.52-0.81; RD −0.01, 95% CI −0.02 to −0.00, P = .01). Length of stay was 3-4 days shorter. There was no probiotic-related sepsis, although this is rarely reported outside trials.6

    Probiotics are still infrequently used in North America. In 2012, only 8%-9% of very low birth weight (VLBW) infants in the Vermont Oxford Network received probiotics.7 It is time to consider changing guidance and practice.8 The authors of this editorial have differed on whether we have sufficient evidence to introduce prophylactic treatment. Tarnow-Mordi et al argued in 2010 that “the evidence that probiotics reduce mortality rates is as conclusive as that for surfactant for respiratory distress syndrome, cooling for hypoxic ischemic encephalopathy, or antenatal corticosteroids for threatened preterm labor.”9 In a companion commentary, Soll argued that the decision was far less clear.10 Trials had used multiple agents and doses. Few had studied extremely low birth weight infants, and few infants had received breast milk.
    Many of these arguments have now been addressed. Wang reports subgroups of trials using Bifidobacteria alone, Lactobacilli alone, or the 2 combined.5 In all 3 subgroups, there were significant reductions, by about two-thirds, in the RR of NEC. The recently updated Cochrane Review includes 17 trials of >4900 VLBW infants.3 The RR risk of severe NEC for probiotics versus control was 0.41 (95% CI 0.31-0.56; RD −0.03, 95% CI −0.05 to −0.02; P < .00001). The treatment of 33 VLBW infants would prevent 1 case of severe NEC. The ProPrems study in 1099 very preterm infants in Australia and New Zealand is the largest ever randomized trial of probiotics.11 Although there was no decrease in sepsis or the control mortality rate of 5.1%, the rate of NEC was halved (4.4% vs 2.2%; RR 0.46, 95% CI 0.23-0.93; P = .03), even though >95% of infants received breast milk.

    Thursday, January 30, 2014

    Gavage Feeding-Continuous or Bolus?

    It is a very well done in-vitro study published in 2010, yet has many practical implications.
    Abstract
    Substantial losses of nutrients may occur during tube (gavage) feeding of

    fortified human milk. Our objective was to compare the losses of key macronutrients and

    minerals based on method of fortification and gavage feeding method. We used clinically

    available gavage feeding systems and measured pre- and post-feeding (end-point) nutrient

    content of calcium (Ca), phosphorus (Phos), protein, and fat. Comparisons were made

    between continuous, gravity bolus, and 30-minute infusion pump feeding systems, as well

    as human milk fortified with donor human milk-based and bovine milk-based human milk

    fortifier using an in vitro model. Feeding method was significantly associated with fat and

    Ca losses, with increased losses in continuous feeds. Fat losses in continuous feeds were

    substantial, with 40 ± 3 % of initial fat lost during the feeding process. After correction for

    feeding method, human milk fortified with donor milk-based fortifier was associated with
    significantly less loss of Ca (8 ± 4% vs. 28 ± 4%, p< 0.001), Phos (3 ± 4% vs. 24 ± 4%,

    p < 0.001), and fat (17 ± 2% vs. 25 ± 2%, p = 0.001) than human milk fortified with a

    bovine milk-based fortifier (Mean ± SEM).
    Continuous Feedings of Fortified Human Milk Lead to Nutrient Losses of Fat, Calcium and Phosphorous.
    Nutrients 2010, 2, 230-240; doi:10.3390/nu2030240
    Stefanie P. Rogers 1, Penni D. Hicks 2, Maria Hamzo 2, Lauren E. Veit 3 and Steven A. Abrams




     
     

    Friday, January 24, 2014

    Chorioamnionitis AND Retinopathy of Prematurity

    http://www.karger.com/Article/FullText/357556

    Abstract
    Background: The role of chorioamnionitis (CA) in the development of retinopathy of prematurity (ROP) has not been well established. Objective: To conduct a systematic review and meta-analysis of the association between CA and ROP in preterm infants. Data Sources: The authors searched MEDLINE, Embase, CINAHL, Cochrane Central Register of Controlled Trials and PubMed, reviewed reference lists of relevant articles, abstracts and conference proceedings (Society for Pediatric Research, European Society for Paediatric Research 1990-2012), sought results of unpublished trials, and contacted the primary authors of relevant studies. Study Selection: Studies were included if they had a comparison group, examined preterm infants, and reported primary data that could be used to measure the association between exposure to CA and the development of ROP. Data Extraction: Two reviewers independently screened the search results, applied inclusion criteria and assessed methodological quality using the Newcastle-Ottawa Scale. One reviewer extracted data and a second reviewer checked data extraction. Summary relative risks (RRs) were calculated using a random effects model. Data Synthesis: We identified 1,249 potentially relevant studies from the electronic databases. Twenty-seven studies involving 10,590 preterm neonates with 2,562 cases of ROP were included. Taking into account all included studies without adjusting for gestational age (GA), CA was significantly associated with ROP (any stage) [summary RR 1.33 (95% CI 1.14-1.55, I2 = 77%, pheterogeneity < 0.0001)], and a borderline significant association was observed for severe ROP (stage ≥3) [summary RR 1.27 (95% CI 0.99-1.63, I2 = 74%, pheterogeneity < 0.0001)]. There was no publication bias with Begg's test. However, subgroup analysis of studies adjusting for GA showed no significant association on CA with ROP [summary RR 0.98 (95% CI 0.77-1.26, I2 = 0%, pheterogeneity = 0.89)]. Conclusion: Unadjusted analyses showed that CA was significantly associated with ROP (any stage) as well as with severe ROP (stage ≥ 3). However, the association disappeared on analysis of studies adjusting for GA. Hence, CA cannot be definitively considered as a risk factor for ROP, and further studies should adjust for potential confounding factors and report results by stage to clarify the association with severe ROP.

    Friday, January 3, 2014

    Postnatal Head Growth in Preterm Infants: A Randomized Controlled Parenteral Nutrition Study


    http://pediatrics.aappublications.org/content/133/1/e120.abstract

    BACKGROUND: Early postnatal head growth failure is well recognized in very preterm infants (VPIs). This coincides with the characteristic nutritional deficits that occur in these parenteral nutrition (PN) dependent infants in the first month of life. Head circumference (HC) is correlated with brain volume and later neurodevelopmental outcome. We hypothesized that a Standardized, Concentrated With Added Macronutrients Parenteral (SCAMP) nutrition regimen would improve early head growth. The aim was to compare the change in HC (ΔHC) and HC SD score (ΔSDS) achieved at day 28 in VPIs randomly assigned to receive SCAMP nutrition or a control standardized, concentrated PN regimen.
    METHODS: Control PN (10% glucose, 2.8 g/kg per day protein/lipid) was started within 6 hours of birth. VPIs (birth weight <1200 1="" 28.="" 3.8="" actual="" assigned="" collected="" control="" daily="" data="" day="" days="" either="" for="" g="" gestation="" glucose="" hc="" intake="" kg="" lipid="" measured="" nutritional="" on="" or="" p="" per="" protein="" randomly="" regimen.="" remain="" scamp="" start="" the="" to="" was="" weekly.="" weeks="" were="">
    RESULTS: There were no differences in demographic data between SCAMP (n = 74) and control (n = 76) groups. Comparing cumulative 28-day intakes, the SCAMP group received 11% more protein and 7% more energy. The SCAMP group had a greater ΔHC at 28 days (P < .001). The difference between the means (95% confidence interval) for ΔHC was 5 mm (2 to 8), and ΔSDS was 0.37 (0.17 to 0.58). HC differences are still apparent at 36 weeks’ corrected gestational age.
    CONCLUSIONS: Early postnatal head growth failure in VPIs can be ameliorated by optimizing PN.

    IVH outcomes in VLBW infants-Outcomes



    http://pediatrics.aappublications.org/content/133/1/55.abstract

    Intraventricular Hemorrhage and Neurodevelopmental Outcomes in Extreme Preterm Infants

    OBJECTIVE: Not many large studies have reported the true impact of lower-grade intraventricular hemorrhages in preterm infants. We studied the neurodevelopmental outcomes of extremely preterm infants in relation to the severity of intraventricular hemorrhage.
    METHODS: A regional cohort study of infants born at 23 to 28 weeks’ gestation and admitted to a NICU between 1998 and 2004. Primary outcome measure was moderate to severe neurosensory impairment at 2 to 3 years’ corrected age defined as developmental delay (developmental quotient >2 SD below the mean), cerebral palsy, bilateral deafness, or bilateral blindness.
    RESULTS: Of the 1472 survivors assessed, infants with grade III–IV intraventricular hemorrhage (IVH; n = 93) had higher rates of developmental delay (17.5%), cerebral palsy (30%), deafness (8.6%), and blindness (2.2%). Grade I–II IVH infants (n = 336) also had increased rates of neurosensory impairment (22% vs 12.1%), developmental delay (7.8% vs 3.4%), cerebral palsy (10.4% vs 6.5%), and deafness (6.0% vs 2.3%) compared with the no IVH group (n = 1043). After exclusion of 40 infants with late ultrasound findings (periventricular leukomalacia, porencephaly, ventricular enlargement), isolated grade I–II IVH (n = 296) had increased rates of moderate-severe neurosensory impairment (18.6% vs 12.1%). Isolated grade I–II IVH was also independently associated with a higher risk of neurosensory impairment (adjusted odds ratio 1.73, 95% confidence interval 1.22–2.46).
    CONCLUSIONS: Grade I–II IVH, even with no documented white matter injury or other late ultrasound abnormalities, is associated with adverse neurodevelopmental outcomes in extremely preterm infants.