Discussion
There are documented benefits from sterile gloves and gown; clean hair covers, masks, and boots; surgical hand washing techniques; and LAF in reducing surgical infections (Hubble et al.
1996;
American Association of Nurse Anesthetists 2013). Moreover, bacterial isolates are increased when LAF is interrupted in an OR by frequent opening of the doors (
Smith et al. 2013). Maintaining sterility of the surgical environment is viewed as even more critical when you have a significantly immunocompromised patient involved (Castro
2008). The ward setting provides unique challenges regarding transmission of infections to SCID patients, as health care providers attend to multiple patients with the potential for transmitting virulent organisms that are “antimicrobial resistant” (
Centers for Disease Control and Prevention [CDC] 2014). Vigilant reverse isolation of SCID patients in LAF can help minimize the risk of hospital-acquired infections. In our first publication of results for unrelated donor transplants for SCID, we reported only 5 episodes of bacterial sepsis in 16 patients undergoing matched unrelated donor BMT with our protocol (Dalal et al.
2000).
There have been few studies and reviews that have questioned the benefit of strict isolation for patients undergoing HSCT (Centers for Disease Control and Prevention; Infectious Disease Society of America; and American Society of Blood and Marrow Transplantation
2000; Sullivan et al.
2001; Yokoe et al.
2009). A recent survey found that even among patients with communicable diseases undergoing HSCT that isolation precautions were not used at many centres (
Hicheri et al. 2013). However, careful analysis of these studies and reviews suggests that the lack of advantage from isolation was based on a lack of survival advantage for adult patients with malignancy undergoing HSCT, and the literature did not look at infectious morbidity. In adults, at least 85% of infections are caused by reactivation of the infection in the host rather than by acquired pathogens (van Kraaij et al.
2002). In contrast, for infants, acquired infections such as EBV, CMV, adenovirus, and varicella are usually transferred to the infant from their caregivers, rather than being host in origin. This factor suggests that more vigilant control of infectious exposure is required for infants, particularly for those with profound cellular immunodeficiencies.
The survival of cancer patients undergoing HSCT is impacted by factors such as disease recurrence and treatment-related morbidity, but these factors are not relevant for patients with nonmalignant diseases. A large study in aplastic anemia, using an isolation protocol similar to ours, demonstrated the importance of the use of a protective environment in reducing mortality (Storb et al.
1983). Isolation has also been shown to benefit HSCT patients by reducing the incidence of nosocomial respiratory viruses (Raad et al.
1997). The benefit of reverse isolation in protecting SCID patients from infections is best evidenced by David, who lived in a “bubble” for 12 years and remained free from severe infections (Guerra and Shearer
1986). It has also been shown that despite normal colonization of the gut and skin for an infant with SCID born by C-section and placed immediately in reverse isolation, the infant remained disease free for a 5-year period; this supports the importance of LAF and reverse isolation techniques in preventing significant infections in SCID patients (Taylor et al.
1978).
A protective environment has also been associated with delayed onset and reduced acute graft versus host disease (GVHD) frequency and severity, as infections may be a trigger for the development of GVHD (Storb et al.
1983). Preventing infections and immune stimulation is particularly important for SCID patients receiving HSCT, because of their increased risk for GVHD reported at >70% in a large multicentre study (Grunebaum et al.
2006). This study found that GVHD and infections were the main cause of morbidity and mortality among these patients. The increased risk for severe and lethal GVHD is not surprising, as patients with immune deficiency have an abnormal/immature immune system with limited “negative selection” capacity (i.e., the ability to remove “auto-reactive” immune cells). Peripheral blood from SCID patients has revealed that they have markedly reduced levels of thymic dendritic and regulatory T cells (Treg), which are critical cells for immune regulation (Poliani et al.
2009; Somech et al.
2009). Treg are not expected to return to normal until after recovery of the thymus in patients with SCID, which occurs months after HSCT and may be even longer if prolonged immunosuppression is required to control GVHD (Cavazzana-Calvo et al.
2007).
The high financial cost of reverse isolation and LAF rooms has been used as an argument for not caring for SCID patients in this environment. A theoretical analysis of the nursing time spent preparing to enter patients’ rooms (2 min hand scrub, mask, gown, and glove) in a 9-bed HSCT unit suggested an annual cost of USD $7000/patient (Hayes-Lattin et al.
2005). However, when costs of providing isolation are offset against the financial cost of increased morbidity from GVHD and added in-patient hospital days the cost of reverse isolation is not so prohibitive.
It has also been argued that reverse isolation might have significant neurobehavioral effects on infants with SCID. Evidence from case reports of patients raised in reverse isolation for 28–52 months, and from David who lived in a bubble for 12 years, has shown no evidence of neurobehavioural problems in these children (Freedman et al.
1976; Dalton
1981;
Mueller 2011). From our unpublished observations of more than 25 years, we have not demonstrated impaired development, beyond that expected from the underlying disease, particularly when adequate social interventions and support are provided. However, the impact of the transplant experience on the development of young infants with SCID still requires further study.
Although studies assessing the effectiveness of a particular isolation protocol for SCID patients are lacking, it is also inappropriate to make deductions regarding required isolation for SCID patients from other patients who are secondarily immunosuppressed undergoing BMT. The unique immunological abnormalities and defective immune selection among patients with SCID supports the need to protect these patients from infections to reduce the morbidity and mortality from infections and GVHD. Our SCID reverse isolation protocol has been shown to have a low infection rate, and it has one of the best outcomes in the world for SCID patients undergoing HSCT.