cranberry987
Mum after ttc 16 cycles
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Hi
I just had an email from the head of midwifery and wonder if anyone can help with the issues shes raised (in spoiler). Theres also a load of new complications mentioned which no one has ever told me before (and have not come up in any of my research). Wondering where theyve come from to be honest.... feeling very suspicious that theyre suddenly trying to scare me into a hospital birth so are bringing out the big guns.
Oh and I have my MW appointment tomorrow, aim was to talk about hb plans there... nice lot of notice theyve given me. Would have been nice if they had brought this up 18 fricking weeks ago when i first mentioned a home birth.
My daily blood sugars are perfect, hba1c 0-24w was 5.2 (will have it redone in 2w), baby measuring 50th% head and body, amniotic fluid and bp perfect, we are both healthy.
Would it be worth me contacting aims?
Thanks in advance
I just had an email from the head of midwifery and wonder if anyone can help with the issues shes raised (in spoiler). Theres also a load of new complications mentioned which no one has ever told me before (and have not come up in any of my research). Wondering where theyve come from to be honest.... feeling very suspicious that theyre suddenly trying to scare me into a hospital birth so are bringing out the big guns.
Oh and I have my MW appointment tomorrow, aim was to talk about hb plans there... nice lot of notice theyve given me. Would have been nice if they had brought this up 18 fricking weeks ago when i first mentioned a home birth.
My daily blood sugars are perfect, hba1c 0-24w was 5.2 (will have it redone in 2w), baby measuring 50th% head and body, amniotic fluid and bp perfect, we are both healthy.
Would it be worth me contacting aims?
Thanks in advance
I have been trying to find a way forward with regard to looking at the possibility of monitoring your babys blood when it is born as it is a minimum requirement to ensure wellbeing of your baby.
I have spoken to several specialists in diabetes and neonatology and companies who make the monitors;
No monitors will guarantee blood sugar recordings below 4mmol which is a problem as your baby is very likely to be below 4 mmols on occasions
The NICE and CMACE diabetes guidance advises no blood sugars need to be monitored before 4 hours post birth even in a baby of a diabetic mother and we would not be at your home realistically after 4 hours.
So I have looked at how else this could be done and drawn a blank once again.
I have spoken to our screening lead and the Trust legal team and whilst it is not illegal for you to test your own babys blood e.g. you draw the blood there are real issues with this;
Damage can be caused to the heel or foot if not taken correctly at all times can result in bone deformity and walking issues at a later stage
Infection
Un-reliable results as discussed above
Specialist training is required to perform this sampling and legally as midwives we are not allowed to teach you to do this having checked with our Trust legal team
One possible solution could be to birth at home and transfer in for the minimal time to allow reliable monitoring of the babys blood sugars although not ideal at least the birth experience would be as you would want and the safety of your baby and wellbeing could be closely monitored.
I have added below some thoughts and research the neonatal team have given me which may or may not be of interest to you
The first bit is there thoughts on the risk to your baby and the subsequent part is some research articles which they felt might be of use to you.
This information is in no way meant to frighten you merely ensure from a neonatal perspective you are aware of all the risks .I suspect you may be aware of many of these risks anyway.
Pulmonary disease
These infants are at an increased risk of respiratory distress syndrome and may present within the first few hours after birth with tachypnea, nasal flaring, intercostal retractions, and hypoxia. Operative delivery due to macrosomia also increases the risk for transient tachypnea of the newborn, whereas polycythemia predisposes the infant to persistent pulmonary hypertension of the newborn.
Initially, the differential diagnosis includes transient tachypnea of the newborn, respiratory distress syndrome, pneumonia, and persistent pulmonary hypertension.
Metabolic and electrolyte abnormalities
Hypoglycemia may present within the first few hours of life. Although the infant is generally asymptomatic, symptoms may include jitteriness, irritability, apathy, poor feeding, high-pitched or weak cry, hypotonia, or frank seizure activity. Hypoglycemia that requires intervention may persist for as long as 1 week.
Hypoglycemia is caused by hyperinsulinemia due to hyperplasia of fetal pancreatic beta cells consequent to maternal-fetal hyperglycemia. Because the continuous supply of glucose is stopped after birth, the neonate develops hypoglycemia because of insufficient substrate. Stimulation of fetal insulin release by maternal hyperglycemia during labor significantly increases the risk of early hypoglycemia in these infants. Perinatal stress may have an additive effect on hypoglycemia due to catecholamine release and glycogen depletion. The overall risk of hypoglycemia is anywhere from 25-40%, with LGA and preterm infants at highest risk.
Hypocalcemia or hypomagnesemia may also be apparent in the first few hours after birth. Symptoms may include jitteriness or seizure activity. Hypocalcaemia (levels < 7 mg/dL) is believed to be associated with a delay in parathyroid hormone synthesis after birth.
Sixty-five percent of all infants of diabetic mothers (IDMs) demonstrate abnormalities of iron metabolism at birth. Iron deficiency increases the infant's risk for neurodevelopmental abnormalities. Iron is redistributed to the iron-deficient tissues after birth, as the red blood cell (RBC) mass is postnatally broken down.
Hematologic problems
Polycythemia, caused by increased erythropoiesis triggered by chronic fetal hypoxia, may present as a clinically "ruddy" appearance, sluggish capillary refill, or respiratory distress. Hyper viscosity due to polycythemia increases the IDMs risk for stroke, seizure, necrotizing enterocolitis, and renal vein thrombosis.
Thrombocytopenia
Thrombopoiesis may be inhibited because of an excess of RBC precursors within the bone marrow as a result of chronic in utero hypoxia and increased erythropoietin concentration.
Hyperbilirubinemia (Jaundice)
This is common, especially in association with polycythemia. The increased red cell mass results in increased number of RBCs that are taken out of circulation each day and increase the bilirubin burden presented to the liver.
References
1. Barnes-Powell LL. Infants of diabetic mothers: the effects of hyperglycemia on the fetus and neonate. Neonatal Netw. Sep-Oct 2007;26(5):283-90. [Medline].
2. Plagemann A. A matter of insulin: developmental programming of body weight regulation. J Matern Fetal Neonatal Med. Mar 2008;21(3):143-8. [Medline].
3. Boney CM, Verma A, Tucker R, Vohr BR. Metabolic syndrome in childhood: association with birth weight, maternal obesity, and gestational diabetes mellitus. Pediatrics. Mar 2005;115(3):e290-6. [Medline].
4. DeBoer T, Wewerka S, Bauer PJ, Georgieff MK, Nelson CA. Explicit memory performance in infants of diabetic mothers at 1 year of age. Dev Med Child Neurol. Aug 2005;47(8):525-31. [Medline]. [Full Text].
5. Bromiker R, Rachamim A, Hammerman C, Schimmel M, Kaplan M, Medoff-Cooper B. Immature sucking patterns in infants of mothers with diabetes. J Pediatr. Nov 2006;149(5):640-3. [Medline].
6. Rosenkrantz TS, Knox I, Zalneraitis EL, et al. Cerebral metabolism and electrocortical activity in the chronically hyperglycemic fetal lamb. Am J Physiol. Dec 1993;265(6 Pt 2):R1262-9. [Medline].
7. Stenninger E, Lindqvist A, Aman J, Ostlund I, Schvarcz E. Continuous Subcutaneous Glucose Monitoring System in diabetic mothers during labour and postnatal glucose adaptation of their infants. Diabet Med. Apr 2008;25(4):450-4. [Medline].
8. Cornblath M, Hawdon JM, Williams AF, et al. Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds. Pediatrics. May 2000;105(5):1141-5. [Medline].
I have spoken to several specialists in diabetes and neonatology and companies who make the monitors;
No monitors will guarantee blood sugar recordings below 4mmol which is a problem as your baby is very likely to be below 4 mmols on occasions
The NICE and CMACE diabetes guidance advises no blood sugars need to be monitored before 4 hours post birth even in a baby of a diabetic mother and we would not be at your home realistically after 4 hours.
So I have looked at how else this could be done and drawn a blank once again.
I have spoken to our screening lead and the Trust legal team and whilst it is not illegal for you to test your own babys blood e.g. you draw the blood there are real issues with this;
Damage can be caused to the heel or foot if not taken correctly at all times can result in bone deformity and walking issues at a later stage
Infection
Un-reliable results as discussed above
Specialist training is required to perform this sampling and legally as midwives we are not allowed to teach you to do this having checked with our Trust legal team
One possible solution could be to birth at home and transfer in for the minimal time to allow reliable monitoring of the babys blood sugars although not ideal at least the birth experience would be as you would want and the safety of your baby and wellbeing could be closely monitored.
I have added below some thoughts and research the neonatal team have given me which may or may not be of interest to you
The first bit is there thoughts on the risk to your baby and the subsequent part is some research articles which they felt might be of use to you.
This information is in no way meant to frighten you merely ensure from a neonatal perspective you are aware of all the risks .I suspect you may be aware of many of these risks anyway.
Pulmonary disease
These infants are at an increased risk of respiratory distress syndrome and may present within the first few hours after birth with tachypnea, nasal flaring, intercostal retractions, and hypoxia. Operative delivery due to macrosomia also increases the risk for transient tachypnea of the newborn, whereas polycythemia predisposes the infant to persistent pulmonary hypertension of the newborn.
Initially, the differential diagnosis includes transient tachypnea of the newborn, respiratory distress syndrome, pneumonia, and persistent pulmonary hypertension.
Metabolic and electrolyte abnormalities
Hypoglycemia may present within the first few hours of life. Although the infant is generally asymptomatic, symptoms may include jitteriness, irritability, apathy, poor feeding, high-pitched or weak cry, hypotonia, or frank seizure activity. Hypoglycemia that requires intervention may persist for as long as 1 week.
Hypoglycemia is caused by hyperinsulinemia due to hyperplasia of fetal pancreatic beta cells consequent to maternal-fetal hyperglycemia. Because the continuous supply of glucose is stopped after birth, the neonate develops hypoglycemia because of insufficient substrate. Stimulation of fetal insulin release by maternal hyperglycemia during labor significantly increases the risk of early hypoglycemia in these infants. Perinatal stress may have an additive effect on hypoglycemia due to catecholamine release and glycogen depletion. The overall risk of hypoglycemia is anywhere from 25-40%, with LGA and preterm infants at highest risk.
Hypocalcemia or hypomagnesemia may also be apparent in the first few hours after birth. Symptoms may include jitteriness or seizure activity. Hypocalcaemia (levels < 7 mg/dL) is believed to be associated with a delay in parathyroid hormone synthesis after birth.
Sixty-five percent of all infants of diabetic mothers (IDMs) demonstrate abnormalities of iron metabolism at birth. Iron deficiency increases the infant's risk for neurodevelopmental abnormalities. Iron is redistributed to the iron-deficient tissues after birth, as the red blood cell (RBC) mass is postnatally broken down.
Hematologic problems
Polycythemia, caused by increased erythropoiesis triggered by chronic fetal hypoxia, may present as a clinically "ruddy" appearance, sluggish capillary refill, or respiratory distress. Hyper viscosity due to polycythemia increases the IDMs risk for stroke, seizure, necrotizing enterocolitis, and renal vein thrombosis.
Thrombocytopenia
Thrombopoiesis may be inhibited because of an excess of RBC precursors within the bone marrow as a result of chronic in utero hypoxia and increased erythropoietin concentration.
Hyperbilirubinemia (Jaundice)
This is common, especially in association with polycythemia. The increased red cell mass results in increased number of RBCs that are taken out of circulation each day and increase the bilirubin burden presented to the liver.
References
1. Barnes-Powell LL. Infants of diabetic mothers: the effects of hyperglycemia on the fetus and neonate. Neonatal Netw. Sep-Oct 2007;26(5):283-90. [Medline].
2. Plagemann A. A matter of insulin: developmental programming of body weight regulation. J Matern Fetal Neonatal Med. Mar 2008;21(3):143-8. [Medline].
3. Boney CM, Verma A, Tucker R, Vohr BR. Metabolic syndrome in childhood: association with birth weight, maternal obesity, and gestational diabetes mellitus. Pediatrics. Mar 2005;115(3):e290-6. [Medline].
4. DeBoer T, Wewerka S, Bauer PJ, Georgieff MK, Nelson CA. Explicit memory performance in infants of diabetic mothers at 1 year of age. Dev Med Child Neurol. Aug 2005;47(8):525-31. [Medline]. [Full Text].
5. Bromiker R, Rachamim A, Hammerman C, Schimmel M, Kaplan M, Medoff-Cooper B. Immature sucking patterns in infants of mothers with diabetes. J Pediatr. Nov 2006;149(5):640-3. [Medline].
6. Rosenkrantz TS, Knox I, Zalneraitis EL, et al. Cerebral metabolism and electrocortical activity in the chronically hyperglycemic fetal lamb. Am J Physiol. Dec 1993;265(6 Pt 2):R1262-9. [Medline].
7. Stenninger E, Lindqvist A, Aman J, Ostlund I, Schvarcz E. Continuous Subcutaneous Glucose Monitoring System in diabetic mothers during labour and postnatal glucose adaptation of their infants. Diabet Med. Apr 2008;25(4):450-4. [Medline].
8. Cornblath M, Hawdon JM, Williams AF, et al. Controversies regarding definition of neonatal hypoglycemia: suggested operational thresholds. Pediatrics. May 2000;105(5):1141-5. [Medline].