Chapter 21: Haematological procedures
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Source: Adapted from Be the Match Registry ([12]).Source: Adapted from Confer et al. ([23]).
Bone marrow harvest
Related theory
Collecting haematopoietic stem cells by means of a bone marrow harvest or apheresis is well established in the transplant setting. More recently, transplants have also been facilitated through stem cells obtained from umbilical cords. Cord blood transplantation remains a specialized procedure more relevant for some areas of transplantation than others (Richardson and Atkinson [98]). The protocol for harvesting this alternative source of stem cells is beyond the scope of this chapter.
Evidence‐based approaches
Rationale
Every year in the United Kingdom about 38,760 people are diagnosed with a haematological malignancy such as leukaemia, lymphoma or myeloma (Haematological Malignancy Research Network [48]). A stem cell transplant is one possible treatment option for these diseases (Atkinson [5]). A stem cell transplant aims to replace a patient's own diseased bone marrow with healthy stem cells. Before the patient receives the stem cells, they receive a combination of chemotherapy and radiation to destroy their own bone marrow. The healthy stem cells are collected from a patient when in remission (autologous) or from a donor (allogeneic) (Richardson and Atkinson [98]). The stem cells are then introduced into the patient's bloodstream much in the same manner as a blood transfusion. If the donated stem cells ‘engraft’, they begin producing normal blood cells (Atkinson [5]). The principles and process of collecting bone marrow apply to both allogeneic and autologous donors.
Indications
Although the use of stem cells collected by apheresis has superseded bone marrow in both the autologous and allogeneic setting in many transplant centres (Richardson and Atkinson [98]), indications for bone marrow harvest include:
- allogeneic donors under the age of 16 years
- allogeneic donors providing cells for a recipient with a non‐malignant disorder, for example aplastic anaemia
- donor preference.
Contraindications
Contraindications to donating stem cells by means of bone marrow include:
- a history of back problems
- donors who are unable to undergo a general anaesthetic.
Principles of care
The care of bone marrow donors is guided by a duty of care, encompassing the physical, emotional, psychological, social and spiritual dimensions of well‐being (Be the Match Registry [12]). Ethical considerations should be incorporated into local policy and guidelines are available that outline the expected standards of care for unrelated (Hurley and Raffoux [60], World Marrow Donor Association [115]) and related (van Walraven et al. [114]) donors. The procedure should be performed as a sterile procedure under general anaesthetic and all perioperative principles apply. Bone marrow harvests are performed under general anaesthesia because:
- The procedure may last for approximately 1 hour compared with 15–30 minutes for an aspiration and biopsy.
- Multiple puncture sites are used.
- The procedure may be painful.
Methods for bone marrow harvest
The procedure is undertaken by:
- two trained practitioners to perform the harvest (either two doctors, or a doctor and a nurse)
- one theatre nurse to oversee the equipment, sterile trolley and infusion of bone marrow into the sterile kit
- theatre staff
- an anaesthetist.
Bone marrow is aspirated directly from the marrow with a bone marrow harvest needle and syringe. A volume of 800–1000 mL is aspirated from the posterior iliac crest (in order to acquire sufficient cells per kilogram of the recipient's body weight) (Outhwaite [90]). The marrow is either frozen and stored or given fresh to the recipient (Richardson and Atkinson [98]).
Anticipated patient/donor outcomes
The anticipated outcome from the procedure is to collect a sufficient dose of stem cells in order to carry out a haematopoietic stem cell transplant. The anticipated outcome for the donor is to:
- remain infection free
- have no nerve, tissue or bone damage
- return to pre‐donation levels of activity within 1 month of the harvest
- adequately manage any pain or discomfort experienced due to the bone marrow harvest.
Legal and professional issues
Standards that regulate bone marrow donation include the Human Tissue Authority ([57]) Code G: Donation of Allogeneic Bone Marrow and Peripheral Blood Stem Cells for Transplantation and FACT‐JACIE's ([40]) International Standards for Cellular Therapy Product Collection, Processing and Administration.
Competencies
It is a requirement that practitioners performing this procedure have experience and training in bone marrow harvesting (FACT‐JACIE [40]). Competence must be demonstrated and documented.
Consent
Before consent is taken, donors should be carefully informed about the risks and benefits of the donation procedure in a manner that they understand. Although transplant centres usually have a preference for the source of stem cells, donors should be given a choice whether to donate bone marrow or stem cells by means of apheresis. Consent is an ongoing process and donors have the right to refuse to proceed (FACT‐JACIE [40]). They should, however, be warned what the consequences of this would be for the recipient, if they do so after the conditioning regimen for transplant has been commenced.
Children acting as donors require further consideration. Laws and regulations governing minors who act as a donor for a sick sibling differ from country to country. Rarely, adult donors with severe developmental or psychological problems rendering them mentally incapable of informed consent are considered as stem cell donors for a relative. These can be either donors who have always been mentally challenged (e.g. Down's syndrome) or those who are suffering from a psychiatric illness. It is advised to first establish whether the aspirant donor would be able to endure the donation procedure (both physically and mentally) before performing tissue type testing (van Walraven et al. [114]).
Pre‐procedural considerations
Equipment
Bone marrow harvest needles are usually 11 G with a removable introducer. Harvested bone marrow must be filtered to remove particulate matter prior to final processing and packaging for distribution or transplantation (FACT‐JACIE [40]). This process must be performed under sterile conditions in the operating room at the time of harvest or in an appropriate sterile setting in the processing laboratory (FACT‐JACIE [40]). Sterile in‐line filters are available commercially in a collection set. The filter size may range from coarse (500 µm) to medium (300 µm) to fine (200 µm). All harvested marrow should ultimately pass through a fine filter, while other sizes may only be necessary if the marrow has a large amount of particulate matter (FACT‐JACIE [40]).
Pharmacological support
The bone marrow harvest is performed under general anaesthesia and local policy with regard to perioperative care should be followed. Local anaesthetic, for example lidocaine 2%, is usually instilled into the harvest sites for postsurgery pain relief. Post‐operative pain should be monitored and is usually managed with non‐opioids and mild opioids. Iron supplements may be prescribed to facilitate haemoglobin recovery post harvest.
Specific patient/donor preparation
There should be donor evaluation procedures in place to protect the safety of the donor and recipient. All stem cell donors (autologous or allogeneic) should be given a medical examination to confirm they are physically and emotionally fit to undergo anaesthesia and the marrow harvest (Be the Match Registry [12]). The donor's medical history, physical examination and laboratory test results should be performed and documented according to the International Standards for Cellular Therapy Product Collection, Processing and Administration (FACT‐JACIE [40]). Both the potential for disease transmission from the donor to the recipient and the risks to the donor from the collection procedure should be assessed (FACT‐JACIE [40]). The allogeneic donor's suitability must be documented before the recipient's high‐dose therapy has begun.
The psychosocial needs of the donor should be assessed (Scott and Sandmaier [102]). Key areas for support are: childcare arrangements, transportation, past and present drug and alcohol usage, unique cultural, religious, literacy and language needs and employment issues (Scott and Sandmaier [102]). An appropriately trained healthcare professional should be available to offer donors counselling, reassurance and support.
Education
It is widely agreed that donors require good‐quality information to reduce their anxiety, to enable them to give informed consent and to enable them to actively participate with the donation process (Chapman and Rush [20], NMC [86]). An increasing number of people are obtaining information from the internet and may be quite informed (or misinformed) based on the quality of the information they acquire. Transplant facilities and donor registries should develop their own centre‐specific information which can be posted on their website or mailed to donors in advance of their first clinic visit to meet some of the education needs (Scott and Sandmaier [102]).
Procedure guideline 21.2
Bone marrow harvest
Table 21.4 Prevention and resolution (Procedure guideline 21.2)
Problem | Cause | Prevention | Action |
---|---|---|---|
Reactions to the anaesthetic agents and associated morbidity (Rosenmayr et al. [99]) | Allergic reactions, hypersensitivity reactions or idiosyncratic reactions (Confer et al. [23]) | Careful preassessment | Instigate urgent treatment and mechanical ventilation as necessary (Confer et al. [23]) |
Haemorrhage, which can result in life‐threatening blood loss and can also create severe pain from the compression of soft tissues (Confer et al. [23]) | Poor technique
Antiplatelet drugs
Anticoagulant drugs
Coagulopathies | Careful preassessment
Experienced practitioners | Pressure dressing
Platelet transfusion
Correction of clotting derangement
Analgesia |
Target cell dose not achieved through aspiration from the posterior iliac crests | This may occur if the marrow space of the crest has been compromised by, for example, trauma or radiation (Confer et al. [23]). This is particularly applicable to autologous donors | Careful preassessment
Experienced practitioners | Marrow may then also be collected from the anterior iliac crests or the sternum (Confer et al. [23]) |
Post‐procedural considerations
Immediate care
Immediate post‐donation care includes:
- all usual post‐operative nursing care measures
- post‐operative full blood count
- adequate analgesia and antiemetic cover
- wound and dressing check before discharge.
Documentation
Bone marrow harvests should be strictly regulated within a quality management system with clear standard operating procedures and documentation. Archived documentation should be maintained according to governmental, regulatory or institutional policy, whichever is longer (FACT‐JACIE [40]). Due to the strict regulatory nature of bone marrow harvests, a record‐keeping system must be in place to ensure the authenticity, integrity and confidentiality of all documents (FACT‐JACIE [40]). All nursing records must be clearly maintained to ensure accurate data (NMC [86]).
Education of patient and relevant others
All donors should be informed that it is normal to experience some pain, bruising and stiffness, feel more tired than usual and run a low‐grade fever during the first week after donation. Soreness at the collection site usually eases off in around a week with pain relief (Be the Match Registry [12]). Further guidelines to be given to donors post procedure are detailed in Box 21.1.
Box 21.1
Guidelines to be given to bone marrow harvest donors post procedure
- The discomfort at the harvest site should resolve in about 1 week.
- Analgesia should be taken as directed.
- Aspirin should be avoided during the first week after the donation unless instructed by the medical team.
- The harvest site should be checked daily for bleeding or increasing erythema.
- The harvest site should be kept dry the night after the procedure.
- Bandages should be removed 24 hours after surgery, and replaced with an adhesive dressing.
- Some wound drainage is expected.
- Showers rather than baths should be taken for the first 2–3 days to decrease the risk of infection.
- The adhesive dressings should be changed daily after a shower until the wounds have healed.
- If bleeding occurs, firm pressure should be applied for 5 minutes, followed by an ice pack. The patient should be advised, if the bleeding does not stop after 10 minutes of constant direct pressure, to contact the hospital.
- It is common to experience ‘hard lumps’ at the harvest sites where the needles were inserted. These may take a few weeks to resolve.
Furthermore, all donors should receive written instructions to contact the hospital if they experience any of the following symptoms (Be the Match Registry [12]):
- temperature of 38°C or higher
- increased redness, bleeding, swelling, drainage or pain at the collection area
- muscle weakness or severe headache within 2 weeks of donation
- pain more than 14 days after the donation.
Complications
The complications of bone marrow harvest are rare but it remains a significant procedure and not without physical risk or psychological consequences (Scott and Sandmaier [102]). There is potential for bone, nerve or other tissue damage at the aspiration sites (Rosenmayr et al. [99]). Sciatic pain, lasting up to 18 months, has been reported in a related donor (Confer et al. [23]). Other complications include:
- A potential for infection at the aspiration sites (Rosenmayr et al. [99]). This may occur due to poor practitioner technique or inadequate wound care. Hand decontamination, infection control and wound care policies should be followed as essential preventive measures (Fraise and Bradley [41]). Antibiotics should be used to treat infections if indicated (Confer et al. [23]).
- Anaemia, due to the large amount of bone marrow aspirated (Rosenmayr et al. [99]). Resultant allogeneic transfusions may cause transfusion reactions or transmit viral infections and, rarely, bacterial infections (Confer et al. [23]). Transfusion practice for bone marrow donation varies depending on the collection physician (see Box 21.2). Discharge medication should include ferrous sulfate.
- Fatigue related to procedure‐induced anaemia. The severity of anaemia is determined entirely by the donor's pre‐operative haemoglobin level and the net blood loss. Treatment with transfusion has already been described. Other measures include:
- a gradual return to work (usually after 1 week)
- ensuring rest between periods of work
- avoiding strenuous activity for 3–4 weeks
- a 1‐month follow‐up appointment for check‐up and repeat full blood count.
In the event of complications, donors should be referred to the medical team, physiotherapist and the wider multidisciplinary team as necessary.
Box 21.2
Reported bone marrow harvest transfusion practice
- Units of autologous blood may be collected from donors a few weeks prior to the harvest for transfusion after the procedure. This practice is becoming less common.
- Autologous red cells may be recovered from the collected bone marrow. This process has been successfully applied in child donors without compromising the quality of the marrow donation.
- Administration of erythropoietin (EPO) may also diminish the likelihood of allogeneic blood transfusion. A theoretical concern about pretreatment of donors with EPO is diminished quality of the collected marrow.