References

Boothman L Platelets in pregnancy: Their role and function in disease. British Journal of Midwifery. 2016; 24:(8)550-5 https://doi.org/10.12968/bjom.2016.24.8.550

British Committee for Standards in Haematology. 2012. http://tinyurl.com/z6zh7l4 (accessed 14 October 2016)

London: DH; 2010

Cines DB, Bussel JB, Liebman HA, Prak ETL The ITP syndrome: Pathogenic and clinical diversity. Blood. 2009; 113:(26)6511-21

Despotovic J, Lambert MP, Herman J RhIG for the treatment of immune thrombocytopenia: consensus and controversy. Transfusion. 2012; 52:(5)1126-36

European Group for Blood and Marrow Transplantation. 2011. http://tinyurl.com/hgm3zon (accessed 14 October 2016)

Fogarty PF, Segal JB The epidemiology of immune thrombocytopenic purpura. Curr Opin Hematol. 2007; 14:(5)515-9

Fogarty PF, Tarantino MD, Brainsky A, Signorovitch J, Grotzinger KM Selective validation of the WHO Bleeding Scale in patients with chronic immune thrombocytopenia. Curr Med Res Opin. 2012; 28:(1)79-87

Gernsheimer T Thrombocytopenia in pregnancy: is this immune thrombocytopenia or…?. Hematology Am Soc Hematol Educ Program. 2012; 2012:198-202

Gernsheimer T, James AH, Stasi R How I treat thrombocytopenia in pregnancy. Blood. 2013; 121:38-47

Kappler S, Ronan-Bentle S, Graham A Thrombotic microangiopathies. Emerg Med Clin North Am. 2014; 3:(32)649-71

Kirkup BLondon: The Stationery Office; 2015

Kistanguri G, McCrae KR Immune thrombocytopenia. Hematology/oncology Clinics of North America. 2013; 27:(3)495-520

Kühne T, Berchtold W, Michaels LA, Wu R, Donato H, Espina B Intercontinental Cooperative ITP Study Group. Newly diagnosed immune thrombocytopenia in children and adults: A comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study Group. Haematologica. 2011; 96:(12)1831-7

Lefkou E, Hunt BJ Bleeding Disorders in Pregnancy. Obstetrics, Gynaecology and Reproductive Medicine. 2015; 11:(25)314-20

Liu D, Ahmet A, Ward L, Krishnamoorthy P A practical guide to the monitoring and management of the complications of systemic corticosteroid therapy. Allergy Asthma Clin Immunol. 2013; 9:(1)

Martí-Carvajal AJ, Peña-Martí GE, Comunián-Carrasco G Medical treatments for idiopathic thrombocytopenic purpura during pregnancy. Cochrane Database Syst Rev. 2009; 2

Mebius RE, Kraal G Structure and function of the spleen. Nature Reviews Immunology. 2005; 5:(8)606-16

McCrae K Immune thrombocytopenia: No longer ‘idiopathic’. Cleve Clin J Med. 2011; 78:(6)358-73

Myers B Diagnosis and management of maternal thrombocytopenia in pregnancy. Br J Haematol. 2012; 158:3-15

London: NICE; 2008

National Maternity Review. 2016. http://tinyurl.com/NMR2016 (accessed 14 October 2016)

National Patient Safety Agency. 2006. http://tinyurl.com/zgu8jlb (accessed 14 October 2016)

NHS Choices. Can I take ibuprofen when I'm pregnant?. 2016. http://www.nhs.uk/chq/pages/2398.aspx (accessed 14 October 2016)

Nicolescu A, Vladareanu AM, Voican I, Onisai M, Vladareanu R Therapeutic options for immune thrombocytopenia (ITP) during pregnancy. Maedica (Buchar). 2013; 8:(2)182-8

London: NMC; 2012

London: NMC; 2015

Parnas M, Sheiner E, Shoham-Vardi I Moderate to severe thrombocytopenia during pregnancy. Eur J Obstet Gynecol Reprod Biol. 2006; 128:(1–022)163-8

Provan D, Stasi R, Newland AC International consensus report on the investigation and management of primary immune thrombocytopenia. Blood. 2010; 115:(2)168-86

Rodeghiero F, Stasi R, Gernsheimer T Standardization of terminology, definitions and outcome criteria in immune thrombocytopenic purpura of adults and children: report from an international working group. Blood. 2009; 113:(11)2386-93

Roytowski D, Figaji A Raised intracranial pressure:What it is and how to recognise it. CME. 2013; 3:(31)85-90

Semple JW, Provan D, Garvey MB, Freedman J Recent progress in understanding the pathogenesis of immune thrombocytopenia. Current opinion in hematology. 2010; 17:(6)590-95

Stasi R Pathophysiology and therapeutic options in primary immune thrombocytopenia. Blood Transfusion. 2011; 9:(3)262-73

Stavrou E, McCrae KR Immune thrombocytopenia in pregnancy. Hematol Oncol Clin N Am. 2009; 23:(6)1299-316

Sukenik-Halevy R, Fejgin M Management of Immune Thrombocytopenic Purpura in Pregnancy. Obstetrical & Gynecological Survey. 2008; 63:(3)182-8

Suri V, Aggarwal N, Saxena S, Malhotra P, Varma S Maternal and perinatal outcome in idiopathic thrombocytopenic purpura (ITP) with pregnancy. Acta obstetricia et gynecologica Scandinavica. 2006; 85:(12)1430-5

Tarantino MD, Young G, Bertolone SJ Single dose of anti-D immune globulin at 75 microg/kg is as effective as intravenous immune globulin at rapidly raising the platelet count in newly diagnosed immune thrombocytopenic purpura in children. J Pediatr. 2006; 148:(4)489-94

Terrell DR, Beebe LA, Vesely SK, Neas BR, Segal JB, George JN The incidence of immune thrombocytopenic purpura in children and adults: A critical review of published reports. Am J Hematol. 2010; 85:(3)174-80

van Veen JJ, Nokes TJ, Makris M The risk of spinal haematoma following neuraxial anaesthesia or lumbar puncture in thrombocytopenic individuals. Br J Haematol. 2010; 148:(1)15-25

Immune thrombocytopaenia in pregnancy: Key principles for the midwife

02 November 2016
Volume 24 · Issue 11

Abstract

Midwives are professionally accountable for detecting deviations from the norm in pregnancy, and initiating referral to an appropriate practitioner. They must work across professional boundaries, particularly where complex conditions require the involvement of doctors, such as immune thrombocytopaenia (ITP) in pregnancy. Most pregnant women with ITP have good outcomes, with only a few requiring first-line treatment. However, close monitoring of maternal and fetal wellbeing are required and appropriate management is crucial in reducing the risk of associated complications.

Midwives are experts in the care of normal pregnancy/birth, but are also professionally accountable for detecting deviations and initiating immediate referral to an appropriate expert (Nursing and Midwifery Council (NMC), 2012). Although the scope of midwifery practice does not include medical diagnosis, as front-line carers, midwives are well placed to make appropriate assessments regarding the health of pregnant women (Chief Nursing Officers of England, Northern Ireland, Scotland and Wales, 2010). Further, it is essential that midwives build a relationship of trust with women and work in partnership, sharing information and consulting regarding their care (NMC, 2015). Care should be tailor-made, offering choices and a service that delivers personalised and safe care for all women and their babies (National Maternity Review, 2016). Midwives are also required to work across professional boundaries (Kirkup, 2015), especially where complex conditions require the involvement of doctors, such as immune thrombocytopaenia (ITP) in pregnancy. Multidisciplinary working is also key to ensure that women receive the correct treatment, particularly when a pregnancy deviates from the norm and becomes high risk owing to an altered health condition.

As an autonomous practitioner, the midwife is viewed as a specialist whose expertise and knowledge base are considered fundamental components in ensuring that women have a safe and life-enhancing experience of childbirth (Chief Nursing Officers of England, Northern Ireland, Scotland and Wales, 2010). It is recommended that each woman should have a named midwife who cares for her throughout her pregnancy. This model of continuity of care can limit the risk to women and babies, preventing incidents and serious adverse outcomes (National Institute for Health and Care Excellence (NICE), 2008). Such integrated models of care are crucial in minimising the potential morbidity associated with ITP (Gernsheimer et al, 2013).

Midwives should be familiar with the change in terminology from ‘idio pathic thrombocytopaenia’ to immune thrombo cytopaenia (McCrae, 2011). This complex condition arises as a consequence of altered immunity; antibodies alter glycoproteins on the surface of platelets, impairing platelet production by rapid destruction of platelets by the spleen (Stasi, 2011). This results in a diminished number of circulating platelets, which, if severe, increases the risk of haemorrhage (Semple et al, 2010; Kühne et al, 2011). In pregnancy, the normal range of platelets is 150–400 × 109/L, which is less than non-pregnant values (Lefkou and Hunt, 2015). The international working group on ITP (Rodeghiero et al, 2009) provided a cut-off for ITP as a platelet count of < 100 × 109/L in the absence of other causes for thrombocytopaenia. Midwives are referred to a recent paper with more detailed discussion on platelet physiology in pregnancy with varying types of thrombocytopaenia (Boothman, 2016); however, the focus of this paper is on ITP. Unlike other autoimmune diseases, ITP is not exacerbated by pregnancy (Parnas et al, 2006; Sukenik-Halevy and Fejgin, 2008); indeed, it is reported that maternal/perinatal outcomes for women with ITP are mostly positive (Suri et al, 2006). Nonetheless, midwives must be aware that although rare (< 1: 1000 pregnancies) possible complications of maternal/fetal haemorrhage may arise (Terrell et al, 2010; Kistanguri and McCrae, 2013). The clinical presentation of ITP may be obscured by signs of normal pregnancy; for example, progesterone-induced bleeding from the gums. However, nosebleeds, bruising and continued bleeding from acu punc ture sites should always be viewed as abnormal and midwives should advise women to report these (Cines et al, 2009; British Committee for Standards in Haematology, 2012). Risk of intracranial bleeding is very rare (< 1: 1 000) and some of the presenting features may mimic pre-eclampsia (e.g. alterations in the visual field and headache) (Fogarty et al, 2012). Other signs and symptoms include: hypertension, bradycardia, nausea and vomiting; all of which are possible signs of raised intracranial pressure (Roytowski and Figaji, 2013). Presentation of these symptoms requires immediate referral to a doctor for a full neurological assessment (NMC, 2012).

Key aspects of care for women with immune thrombocytopaenia

Antenatal

Booking history and case note review

Although a full history is always important as part of a risk assessment, midwives should note that neither age, gender nor ethnicity confer protection against ITP (Fogarty and Segal, 2007). Ibuprofen should be avoided in pregnancy (NHS Choices, 2016); however, women should be reminded that this drug, along with aspirin, is contraindicated with ITP due to the effect on platelets (Myers, 2012). A dental hygiene assessment should be sought for gingivitis. The pattern of care should be tailored specifically for women with ITP; this must be obstetrician-led in conjunction with midwifery care and specialist haematologist input. Antepartum assessments should take place monthly in the first two trimesters, every 2 weeks after 28 weeks, and weekly from 36 weeks up to birth (Provan et al, 2010). Women with ITP may already be members of a national support organisation, but if not, the midwife should direct them to such groups (Box 1).

Support organisations


ITP Support Association www.itpsupport.org.uk
ITP Foundation www.itpfoundation.org

ITP–immune thrombocytopaenia

An assessment by the anaesthetist should be undertaken in the antenatal period to review platelet function prior to labour and birth; a plan of care should be documented in the case notes.

Serum testing

ITP may present early in the first trimester; however, in the absence of bleeding and a platelet count under 30 × 109/L in the second trimester, women only require ongoing assessment. In the third trimester, as labour and birth approach, higher platelet counts (> 50 × 109/L) are required (Kappler et al, 2014). Where counts do not fluctuate, they should ideally be assessed monthly and at least once per trimester (Nicolescu et al, 2013). Midwives should ensure all blood results are suitably recorded and retained and that a doctor has indicated all results have been reviewed.

Treatment

This is only required where there is evidence of bleeding or the platelet count is below 20 000. The main treatment options include the following:

  • In pregnancy, the primary option is the use of oral corticosteroids, usually prednisone (10–20 mg/day). Steroids suppress the immune response, thus increasing the platelet count. However, the midwife and obstetrician must be aware that in women who are hypertensive or have diabetes, steroids should be avoided as they can exacerbate these conditions (Martí-Carvajal et al, 2009; Liu et al, 2013)
  • For women in whom steroids are contra-indicated or where there is an unsuccessful response to steroids, intravenous immunoglobulin (IVIG) may be administered if platelet count is below 10 000 prior to delivery (European Group for Blood and Marrow Transplantation, 2011). The midwife should be aware that vomiting, headache and hypotension may arise as a result of treatment; however, these may be modified by a reduced rate of infusion. All adverse reactions should be reported immediately
  • Anti-D immunoglobulin may be administered, possibly to increase the survival rate of immunised platelets (Tarantino et al, 2006); however, there is no widespread agreement on its use (Despotovic et al, 2012)
  • Platelet transfusions can increase the platelet count over a short period of time and may be considered for those women who are undergoing operative delivery and there are concerns about imminent bleeding (Provan et al, 2010). As with the administration of blood transfusions, midwives are required to have appropriate haemovigilance training and assessed as competent to monitor women (National Patient Safety Agency, 2006)
  • Splenectomy is reserved for only the most resistant/severe cases as, although platelet turnover is reduced, infection risk is increased. This is because the spleen produces anti bodies against infection (Mebius and Kraal, 2005) and infection may further reduce platelets. Hence, with ITP, midwives must be vigilant for reported symptoms/signs of infection and refer to a doctor for immediate review. However, this would be assessed and undertaken post-pregnancy
  • Information sharing and record keeping are key to preserving the safe and effective care of the woman and baby (NMC, 2015).
  • Intrapartum

    Owing to the risk of haemorrhage after birth, women with ITP should be advised to give birth in a fully equipped maternity unit with easy access to blood transfusion. Lower platelet levels will have an impact on the availability of epidural (> 80 × 109/L is required for epidural) and on the management of third-stage blood loss (van Veen et al, 2010). The mode of delivery is determined by maternal condition, and elective caesarean section does not improve outcomes (Provan et al, 2010). However, before surgery or anticipated operative vaginal delivery, platelet count should be taken and should be higher than 50 000 to minimise the risk of bleeding (Gernsheimer, 2012). Midwives should ensure the anaesthetist is informed of the woman's admission to the labour ward, recent platelet results accessed and a wide-bore cannula sited. All of these measures are precautionary in the event of excess bleeding in the third stage of labour. The risk of bleeding may persist in the immediate postpartum, thus close monitoring of blood loss by the midwife is required. All loss and clinical observations must be clearly documented (NMC, 2015).

    Postpartum

    The risk of fetal ITP is high due to antiplatelet IVIG antibodies, which may enter fetal circulation via the placenta and cause fetal thrombo-cytopaenia; this may not be evident until 2–5 days postpartum. Consistent observation and assessment of the neonate is required because, in 5–10% of cases, the thrombocytopaenia is severe (Kistanguri and McCrae, 2013) and may require admission to a neonatal unit. Neonates should be carefully monitored for signs of neurological deficit, which may indicate intracerebral bleeding; however, this risk is very low (Stavrou and McCrae, 2009). Women should be educated about the signs and symptoms and informed on how to request urgent assistance.

    Conclusions

    Most women with ITP have good outcomes in pregnancy with only a few requiring first-line treatment. However, close monitoring of maternal and fetal wellbeing are required to detect complications. Midwives should ensure women are given adequate antepartum appointments with one-to-one care being the ideal; there should be an opportunity to provide contact details of support groups. Clear information on the signs and symptoms of a falling platelet count with clarification on when to seek medical or midwifery advice should be provided. Midwives may help to minimise complications by advising women to avoid certain medications. Elective operative delivery does not provide better maternal or fetal outcomes over vaginal birth, but options for analgesia may be limited. Midwives must ensure all women with ITP who are in labour have been assessed by the medical team and that intravenous access is maintained in the event of severe bleeding. Diligent management of the third stage of labour is even more crucial for women with ITP and close observation for postpartum bleeding should ensue. Finally, the midwife must be aware that a small proportion of neonates may present with signs and symptoms of bleeding and this may take several days to manifest.

    Revalidation claim: Continuing professional development/40 hours

    This section provides an example of how this article might be used as material for reflection for use as part of a midwife's revalidation with the Nursing and Midwifery Council (NMC). Evidence for revalidation should be linked to the NMC Code and should demonstrate the impact that the learning has had on your practice.


    Nursing and Midwifery Council Code Description Focus of revalidation claim √
    Prioritise people Act in the best interest of people (service users) at all times
    Practise effectively Use best available evidence to assess client need and deliver treatment/care/advise on care
    Preserve safety Work within your skills and knowledge (competence) and use your skills and knowledge to keep people (clients) safe
    Promote professionalism and trust Act in line with the standards of practice and behaviour to uphold the reputation of the nursing and midwifery professions

    Nursing and Midwifery Council (2015) The Code: Professional standards of practice and behaviour for nurses and midwives. NMC, London


    Questions to consider Example answers
    What did you think about on reading this clinical practice article? This article was useful for increasing my awareness of contemporary issues around immune thrombocytopaenia (ITP). This complication of pregnancy poses risks for labour and birth. The article summarised key priorities of care, providing reference sources to promote evidence-based practice
    Why do you think the content made you feel like this? The content of the article reassured me that my current level of understanding is contemporaneous and allowed me to access further reading
    What did you learn as a consequence of reading the article? The article gave a general overview of ITP with areas of good practice recommended by national bodies. In particular, it allowed to me reflect on the possible dangers of a low platelet count in pregnancy e.g. postpartum haemorrhage. This reminded me of my professional accountability in respect of the Nursing and Midwifery Council (NMC, 2012) Midwives rules and standards and Rule 5: Scope of Practice. It also made me reflect on the role of the midwife in demonstrating compassionate care by communicating with women, offering reassurance and acting as an advocate (NMC, 2015).

    Nursing and Midwifery Council (2012) Midwives rules and standards. NMC, London

    Nursing and Midwifery Council (2015) The Code: Professional standards of practice and behaviour for nurses and midwives. NMC, London


    Questions to consider Example answers
    What have you done to complete the learning? I read two further articles: Myers B (2012) Diagnosis and management of maternal thrombocytopenia in pregnancy. Br J Haematol 158(1): 3. doi: 10.1111/j.1365-2141.2012.09135.x Martí-Carvajal AJ, Peña-Martí GE, Comunián-Carrasco G; (2009) Medical treatments for idiopathic thrombocytopenic purpura during pregnancy. Cochrane Database Syst Rev (4): CD007722. doi: 10.1002/14651858.CD007722.pub2 The first article outlined evidence-based principles of care and the second discussed risks of steroids
    What is the effect of your learning? This article included the British Committee for Standards in Haematology guidelines on management of ITP. This reminded me that signs/symptoms should be treated seriously. Midwives must act within their rules and ensure immediate referral
    What will you do differently as a result of reading the article? I will use the article with student midwives to discuss the outcomes for ITP pregnancies, careful history taking and rapid referral. In discussing the evidence, I will refer to: Parnas M, Sheiner E, Shoham-Vardi I et al (2006) Moderate to severe thrombocytopenia during pregnancy. Eur J Obstet Gynecol Reprod Biol 128(1–2): 163–8

    Key Points

  • Most women with immune thrombocytopaenia (ITP) have good outcomes in pregnancy
  • Women with ITP should be given contact details of support groups
  • Clear information on the signs and symptoms of a falling platelet count and when to seek medical or midwifery advice should be provided
  • Midwives must facilitate close monitoring of maternal and fetal wellbeing to detect complications
  • Diligent management of the third stage of labour is crucial for women with ITP, with close observation for postpartum bleeding