Hamed

In our unit, we add MCT oil 0.5 ml/feed in case of VLBWI and LBWI after reaching full feeds with full fortification if not gaining weight according to their growth curves. Special cases, if a preterm with PDA we do a mild restriction of fluids 120 to 130 ml/kg/d and increase caloric intake with addition of MCT oil 0.5ml /feed. We do not use olive oil at all, according to my understanding olive oil is a LCT, not a MCT. @agoz do you use olive oil in your unit? It would be interesting to know more about it.

@agoz this is a nice subject to discuss, thanks, In our unit if the newborn was born inhouse, we give antibiotics to patients with TTN only if there is an indication for administrating antibiotics beside TTN. i.e. TTN is not an indication per se for administrating antibiotics. However, for patients born in other hospitals or maternal centers and transferred to our unit we do administer antibiotics for 48hrs ampicillin and gentamicin until we receive culture results of no growth. @manuel perez valdez In our unit our main target of treatment in decrease WOB by mostly nCPAP (with a PEEP of 6cmH2O) or less commonly HHHFNC (with a flow of 8 L). Oxygen supplementation only to keep saturations (SpO2) within the target range for GA. If FIO2 needs increases reaching to 40% or above besides giving a nCPAP of 6cmH2O, or high pCO2 causing respiratory acidosis, we would consider Biphasic nCPAP 10/6 or NIPPV or intubation and surfactant.

Thanks a lot @HickOnACrick for sharing this case and updating us on it. I am looking forward to hear further updates whenever you can. I have a concern about initial placing a resp. distress case on HFNC less than 8LPM. Is 5 LPM the standard starting flow used in your NICU? The pressure given by the HFNC is variable, but in our NICU we usually consider it is about 1 to 1.5 cmH2O less than a nCPAP with the same PEEP figure, and thus using a HFNC of 5 L would possibly give a PEEP of 3.5~4 cmH2O. Would you please let us know how were babies nearby this case or infants cared by the same nurses caring for this one managed?

Any advice for diagnosis and management of case with Bronchopleural fistula? (and if the Bronchopleural fistula was in case of ChILD would your management differ)?

Here the government officially recommended using any type of masks a starting from 1st week of April. As for health workers, hospitals recommending using surgical masks a couple of weeks earlier, and for workers to limit the number of masks they use/day. This week putting on surgical masks in hospitals was strengthen. N95 masks and other PPEs are only to be used in our NICU if a "confirmed" COVID-19 infected mother was to give birth, which we still didn't experience, and their use are limited to the NICU members who resuscitate this newborn.

Only when showing post-extubation stridor agree with @bimalc Although, @Pototo I would like to know did you mean Racemic epinephrine (before or after extubation)?

@Lenks I do agree with @bimalc, as many of these cases are transient and seem to resolve spontaneously without any specific treatment. In case high Ca intake is suspected to be the cause of hypercalcemia, discontinuing powdered human milk fortifier or preterm formula to first stop this extra intake and closely monitor serum calcium levels without immediate further evaluation. Additionally consider temporarily discontinuing vitamin D supplementation if providing. In case spontaneous correction of serum Ca doesn't take place further invitations as mentioned above with adding renal ultrasound when hypercalciuria is present.

Routinely, we would confirm umbilical lines with a cross table lateral view additionally to the AP view. Although, in the X-ray kindly presented here I do agree with @bimalc the UVC is mal-positioned and no need for a later view. This UVC could be pulled back to be 2 cm below the level of the base of the umbilical stump = (2 cm + length of the umbilical stump) and be used as a low line = (as a peripheral line) /Or if still a central line is indicated a PICC could be placed. I would revise the need of a central line in this infant. In the scenario if this infant was just being resuscitated after delivery and this UVC was just placed in and still the area around the umbilicus is sterile, trying to replace this UVC with a new one, the new UVC will usually follow the track made by the first one. Another way is, if the opening of the umbilical vein could accommodate passing another UVC through without removing the first one, the new UVC could pass in the correct direction. A gentile pressure on the liver downwards and medialy would facilitate passing the UVC in the proper direction.

Same here in Japan, as well as in our unit in Canada, no special management for preterm infants of smoking mothers. Although we have a concern towards smoker parents when they visit their babies in the NICU, we do ask them not to smoke before coming to the NICU and to wear newly washed cloth which doesn't have smoking smell in them.

@Lenks Concerning hypercalcemia (total Calcium of 12 mg/dL is our cutoff for IV saline 10-20 ml/kg with 1 mg/kg lasix. A persistent hypercalcemia in-spite the lasix and total Calcium above 14 mg/dL we would consider glucocorticoids. No experience with bisphosphonates. Calcium intake should be thoroughly reviewed. Although day 7 is early for subcutaneous fat necrosis to cause hypercalcemia, but checking for sites of it could be advised, Further lab. data to know the etiology: ionized calcium, pH, albumin, phosphorus, alkaline phosphatase, PTH, urine sample for spot calcium/creatinine ratio, 25 OH Vit D and 1, 25 OH Vit D. Ask mother and father for Familial hypocalciuric hypercalcemia (autosomal dominant) or check their urine spot calcium/creatinine ratio.

@AntonioPCam thanks a lot, I think contactless monitoring would really be helpful in the NICU. Wishing you all the best.

Concerning the need for intubation and Mech. vent. I concord with @bimalc, @Stefan Johansson and @rehman_naveed and once in during cooling it will remain in until the end of cooling or until an MRI is taken at 4~5 days of life. As for comfort, we do as @rehman_naveed, we give low dose morphine infusion 5 mcg/kg/h not exceeding 10 mcg/kg/h or fentanyl 0.5 mcg/kg/h not exceeding 1 mcg/kg/h (fentanyl preferable for hemodynamic compromised infants). Coming to the timing of MRI, it may vary according to each hospital`s protocol. In addition, it really depends on what you want to see, diffusion and metabolic changes preferably 4~5 days of life, and that concord with 24 to 72 hrs after cooling as @bimalc. Brain injury changes continue to develop as late as the 2nd week of life. That is why you find some units do the MRI at day 4~5 or day 7 or end of 2nd week of life.

Hi @Andrej Vitushka thank you for your question and discussion, it opened up a lot of thoughts. Sorry for seeing your question so late, @Stefan Johansson kindly answered. Thanks Stefan.

Hi @Andrej Vitushka you can use both central or capillary. For cutoffs please check the PINT study. We use table 1 low threshold cutoffs for transfusion. https://www.ncbi.nlm.nih.gov/pubmed/16939737 PINT trial.pdf

Unfortunately, not using LMAs in our Perinatal-neonatal center.