Acutely ill newborns require prompt and correct treatment. Certain neonatal diseases carry a very high risk of recurrence in the woman’s subsequent pregnancies and births. In such cases, targeted preventive measures must be considered.
Figure 1 MRI of head, T2 image with 1.5 Tesla scanner. The images during the first day of life show a) fresh subdural haematomas (arrows) and b) mixture of fresh and 3 – 4 day-old intracerebral haematomas (arrows). c) Control after 24 hours shows an increase in the size of one intracerebral haematoma (arrow). d) After 15 months a cavity remains frontally after the largest intracerebral haematoma (arrow)
Thrombocytopenia is found in about 1 % of all newborns (
1 – 3). The causes are usually divided into two main categories: reduced production and increased consumption/destruction. The cause of reduced production may be hereditary thrombocytopenia, infection (bacterial, viral, fungal) or toxic effect on bone marrow due to maternal medication. Increased destruction may be due to immunological conditions (auto- or alloantibodies), peripheral consumption (hypersplenism, Kasabach-Merritt syndrome, disseminated intravasal coagulation (DIC) or iatrogenic factors (e.g. replacement transfusion)). A correct diagnosis is made on the basis of the medical history of mother and child, a thorough clinical examination of the child and laboratory tests. Severe cases of thrombocytopenia, defined as a concentration of less than 50 · 10⁹ cells/l, are most frequently found to be alloantibody-mediated thrombocytopenia ( 4).
Platelets have many different platelet-specific antigens (human platelet antigen, HPA) on their surfaces, and 13 biallelic HPA systems have been identified. The two alleles in each system are called
a and b; a is common and b is rare ( 5, 6). HPA-1a immunisation is most often the cause of fetal/neonatal alloimmune thrombocytopenia (FNAIT). 98 % of all Caucasians carry the HPA-1a antigen in either double (homozygous) or single (heterozygous) dose; the remaining 2 % are homozygous for the HPA-1b antigen, i.e. their phenotype is HPA-1bb ( 4). Alloimmunisation with HPA antigens may occur in connection with incompatible pregnancies or, more rarely, with transfusions.
Women with platelet phenotype HPA-1bb may produce alloantibodies against HPA-1a in the course of their pregnancy if the fetus has inherited the HPA-1a antigen from its father. The maternal alloantibodies are of type IgG and can cross the placenta and bind to the surface of fetal platelets, which are then destroyed. The woman will have a normal platelet count and may be immunised during her first pregnancy (25 %) or in connection with delivery (75 %). Thus the fetus may be affected in the first pregnancy (
7). This is in contrast to antibody-mediated haemolytic disease in neonates, where the problem seldom arises during the first pregnancy, but most often in subsequent incompatible pregnancies after immunisation.
In fetal/neonatal alloimmune thrombocytopenia the fetus may develop serious thrombocytopenia and haemorrhage already in utero (
5, 6). In the literature, the incidence of FNAIT is reported to be one in 1 000 – 2 000 newborns ( 8, 9). This means that 30 – 60 neonates are affected each year in Norway. In most cases, the condition is not associated with serious haemorrhagic complications, but intracranial haemorrhage occurs in 7 – 26 % of cases, with neonatal mortality in about one third ( 8).
Up to the present, no country has introduced screening of pregnant women to identify HPA-1a-negative women or detection of HPA-1bb women with anti-HPA-1a antibodies. As a rule, the diagnosis of fetal/neonatal alloimmune thrombocytopenia has been made after the birth of a baby with severe thrombocytopenia and haemorrhage. This means that the possibility of taking preventive steps is limited to pregnancies where the woman has previously given birth to a child with this diagnosis.
We have described the neonatal medical histories of two siblings with fetal/neonatal alloimmune thrombocytopenia. The condition was neither known nor suspected in the first child before birth. Unusually intensive and prolonged treatment was required, and cerebral haemorrhage was detected. In the next pregnancy, the condition was expected, and mother and child were closely monitored before, during and after the birth. The course and outcome were different in this case. Child number two also had severe thrombocytopenia at birth, and the maternal antibody level during pregnancy was very high. This child needed several transfusions of HPA-1bb (compatible) platelets. We believe it is likely that early delivery and rapid intravenous administration of HPA-1bb platelets and immunoglobulin to the second child prevented organ haemorrhage and inhibited platelet destruction, and the course was less serious.
The birth of the first child up until surgical delivery took place was protracted. The intracranial haemorrhage was fresh at the time of birth (Fig. 1). One may wonder whether this could have been avoided if the maternal platelet type and antibody level during pregnancy had been known, and a caesarean section had been performed 2 – 3 weeks before term, with compatible platelets available for the child.
The clinical course of fetal/neonatal alloimmune thrombocytopenia is variable, and ranges from a slightly decreased thrombocyte count with spontaneous normalisation, to severe thrombocytopenia with intracranial haemorrhage and neonatal death. A correlation between the maternal antibody level and infant platelet count has been demonstrated in several studies (
7, 9). It has also been shown that antenatal treatment of the mother with intravenous injection of IVIg and steroids can reduce the incidence of cerebral haemorrhage ( 9, 10).
Approaches in the event of known risk of fetal/neonatal alloimmune thrombocytopenia vary from country to country. In the past, fetal blood testing (platelet counts) and platelet transfusions were performed, but as a general rule this is not done today because the procedure entails a high risk of haemorrhagic complications (
11). In Norway, mothers are rarely treated with IVIg during pregnancy, but we believe this is likely to be recommended in the future as the standard treatment for women who have previously given birth to babies with cerebral haemorrhage induced by fetal/neonatal alloimmune thrombocytopenia. Special monitoring in the later stages of pregnancy should be offered under any circumstances if a woman has given birth to a child with this condition. In our view this follow-up should consist of repeated analyses and quantification of anti-HPA-1a platelet antibodies and a recommendation for an elective caesarian section 2 – 3 weeks before term, with HPA-1bb platelets available (fig 2). Alternatively, platelets from random donors can be combined with intravenous injection of IVIg until HPA-1bb platelets can be procured.
Figure 2 Our proposal for diagnosis, treat-ment and further follow-up in con-nec-tion with fetal/neo-natal alloimmune thrombo-cyto-penia
There is debate in Norway and internationally on screening and prevention and treatment procedures of FNAIT(
12 – 15). In 2008 the Norwegian Directorate of Health appointed a working committee to consider screening for FNAIT. The committee was not in favour of introducing the screening, but recommended further research ( 16). There are now plans for testing prophylaxis against immunisation ( 17, 18). The introduction of this prophylaxis will require HPA-1 typing of all pregnant women to identify candidates for treatment. There is also research in progress to neutralise antibodies in mothers who are already immunised ( 19).
The two cases illustrate that FNAIT is a serious condition that can occur in the first pregnancy, but planning of delivery and neonatal treatment makes no provision for firstborns. Correct neonatal treatment requires knowledge of the diagnosis to prevent or limit complications. Ongoing Norwegian and international studies may lead to a change in the current strategy for detection, follow-up and treatment of FNAIT.