medical device-related pressure injury, pediatrics, pediatric risk assessment, pressure injuries, pressure injury prevention, pressure ulcers, white paper



  1. Delmore, Barbara PhD, RN, CWCN, MAPWCA, IIWCC-NYU
  2. Deppisch, Michelle PT, CWS, FACCWS
  3. Sylvia, Cynthia DNurs, MSc, MA, RN, CWCN
  4. Luna-Anderson, Crystal BSN, RN, CWON, CFCN
  5. Nie, Ann Marie MSN, RN, FNP-BC, CWOCN


GENERAL PURPOSE: To review what is known about pediatric pressure injuries (PIs) and the specific factors that make neonates and children vulnerable.


TARGET AUDIENCE: This continuing education activity is intended for physicians, physician assistants, nurse practitioners, and nurses with an interest in skin and wound care.


LEARNING OBJECTIVES/OUTCOMES: After participating in this educational activity, the participant should be better able to:


1. Identify the scope of the problem and recall pediatric anatomy and physiology as it relates to PI formation.


2. Differentiate currently available PI risk assessment instruments.


3. Outline current recommendations for pediatric PI prevention and treatment.


ABSTRACT: Pediatric patients, especially neonates and infants, are vulnerable to pressure injury formation. Clinicians are steadily realizing that, compared with adults and other specific populations, pediatric patients require special consideration, protocols, guidelines, and standardized approaches to pressure injury prevention. This National Pressure Advisory Panel white paper reviews this history and the science of why pediatric patients are vulnerable to pressure injury formation. Successful pediatric pressure injury prevention and treatment can be achieved through the standardized and concentrated efforts of interprofessional teams.


Article Content


Pediatric pressure injuries (PIs) are increasingly recognized as a source of possible iatrogenic harm, morbidity, suffering, and increased costs.1,2 The National Pressure Ulcer Advisory Panel (NPUAP) initially drew attention to this problem in a 2001 monograph on PI prevalence and incidence.3 This was followed by additional data in the 2012 NPUAP incidence and prevalence monograph.4 The 2014 NPUAP, European Pressure Ulcer Advisory Panel (EPUAP), and Pan Pacific Pressure Injury Alliance (PPPIA) International Guideline devoted an entire chapter to the prevention of PIs in pediatric patients.5 Much has been learned since those initial efforts to elucidate this critical problem.


The purpose of this article is to review what is known about pediatric PI and the specific factors that make children so vulnerable. The authors describe the scope of the problem; pediatric anatomy and physiology as it relates to PI formation; and the current recommendations for pediatric PI prevention and treatment, including 18 selected skin and PI risk assessment instruments.


Scope of the Problem

Goudie and colleagues6 looked at the costs of stages 3 and 4 PIs and found that the average PI costs were nearly $20,000 per injury. In patients between 1 and 4 years of age, the average cost was $85,853;6 when multiplied by available prevalence and incidence data, the cumulative cost is astounding. In general, PIs are reported as prevalence and incidence data with varying formulas.5


Early pediatric studies (2010 or earlier), including multicenter studies, reported pediatric PI prevalence estimates ranging from 0.47% to 35%.7-16 Pediatric ICUs (PICUs) have higher prevalence estimates, ranging from 7.1% to 44%.16-18 Schluer and colleagues16 reported an estimate of 43% in their neonatal ICU (NICU). Facility-acquired pediatric PIs often comprise a substantial portion of these injuries.11 In one study of nine ICU units, authors reported an 8.7% prevalence estimate; 3.4% of the PIs were facility-acquired.11


Earlier incidence data (2010 or earlier), which may be reported in the literature as a percentage or as incidence density, demonstrated higher incidence in ICUs. For example, incidence may range from 0.29% to 7.2%.7,19 In PICUs, however, the reported incidence ranged from 7% to 27%.13,20-24 In NICUs, incidence percentage was reported between 8% and 16%.25,26 Expressed as incidence density, Visscher and colleagues20 reported 14.3/1,000 patient-days in the PICU (preimprovement effort; postimprovement effort, 3.7/1,000 patient-days) and 0.9/1,000 patient-days in the NICU regardless of improvement effort.


In general, there is little change between the prevalence and incidence data collected before or in 2010 as compared with data collected 2011 and later. Prevalence estimates after 2010 have ranged from 1.4% to 8.2%,27,28 whereas critical care areas report prevalence as high as 43.1%.28 In a more recent study of hospital-acquired PI (HAPI), Razmus and Bergquist-Beringer28 found that prevalence was highest among children aged 9 to 18 years (1.6%) and then those aged 5 to 8 years (1.4%). Critical care (3.74%) and rehabilitation units (4.6%) had the highest HAPI prevalence. The lowest HAPI prevalence estimate was in general pediatric units (0.57%).


Incidence data reported after 2010 tend to be reported as incidence density in relation to quality improvement efforts. For example, Peterson and colleagues29 reported data both pre- and postimprovement (2010 to 2014). Before their improvement effort, incidence was 3.3/1,000 patient-days (second quarter 2010), which was reduced to 1.7/1,000 patient-days postimprovement (second quarter 2014). Frank and colleagues1 saw a reduction in stages 3 (0.06-0.03/1,000 patient-days) and 4 PIs (0.01-0.004/1,000 patient-days) after an improvement effort.


Devices are a leading cause of PIs in the younger pediatric population (neonates and children).2,15,30 Medical devices may account for 38.5% to 90% of PIs,15,16,20,25 and patients with this type of PI tend to be younger.25,26 For example, Visscher and Taylor25 evaluated NICU patients between 2007 and 2009. They found that nearly 80% of the PIs were associated with devices, and more than 90% of device-related PIs occurred in the premature infants. The authors also suspected that the higher estimates in the NICU indicated a "susceptibility to iatrogenic injury in pediatrics."25 Early studies (published before 2010) did not always separate out device-related PIs or specify whether device-related PIs were included or excluded.31


Respiratory devices are particularly problematic. For example, in their progressive care unit, Miske and colleagues32 found 35 PIs; approximately half were caused by tracheostomy securement devices (fiscal year 2015). Four months after practice change (performing neck assessments every shift), there was a decrease in securement device-related PIs to zero. However, the authors found it challenging to sustain these efforts and maintain this result.32


Although it is prudent to use prevalence and/or incidence data to determine if a problem exists and successfully address it, this appears to be easier said than done. Challenges include misunderstandings regarding terms and definitions of prevalence and/or incidence, failure to clearly define the study population, lack of resources for data collection, inability to distinguish between wounds and PIs, failure to acknowledge that devices can cause PIs, and errors in data analysis and interpretation.33,34 Further, providers should exercise caution when comparing data points from earlier years with those from more recent years because there are differences in the parameters included or excluded (eg, PIs only or PIs and other wound types), methodologies employed, single versus multiple sites, terminology, classification, and study quality.13,31,33 There have also been revisions to the NPUAP staging system during the years that these studies were conducted.



Much of the vulnerability to PIs can be appreciated given an understanding of pediatric skin development and maturity. Many skin issues, including PIs, are attributable to skin immaturity and body size and further compounded by the need for ventilation and invasive technologies to improve survival rates in young patients.26,35


Pediatric skin maturity certainly differs from adults, yet differences also exist among pediatric populations. Neonates and infants younger than 2 years are considered especially vulnerable.21 Makimoto and colleagues36 noted PI damage as early as day 12 on a patient born at 24 weeks of gestation and weighing 653 g. A recent case series highlighted three infants (two premature, one full-term) believed to have developed PIs in utero, termed "congenital PIs."37


The pediatric population can be categorized by age, birth-weight classification, and a combination of birth-weight classification and gestational age (Table 1).38-42 There may be some overlap or different terminology used to categorize the pediatric population, but it is important to understand that skin anatomy differences and a variety of factors can contribute to pediatric propensity to skin injuries. According to the 2014 NPUAP, EPUAP, PPPIA International Guideline, impairments in skin condition are associated with higher incidence of PIs.5 Therefore, it is critically important to maintain optimal skin conditions to prevent PIs as pediatric skin matures. For example, as seen in seminal and more recent work, the neonate's vulnerability to skin injuries can be attributed to certain key structures that are underdeveloped, diminished, or unstable, and these may be interrelated.43 Daily care such as bathing, moisturizing, or removing adhesives can disrupt normal barrier function, putting neonates at risk of PI formation.43,44


In neonates, the stratum corneum is thinner and has only two or three layers.43,45 To put this into perspective, the adult and full-term infant have 10 to 20 layers of stratum corneum. The ruddy appearance common in neonates is because of these few layers of stratum corneum. Therefore, assessing oxygenation using skin color in neonates is a poor method.43 In neonates younger than 24 weeks' gestational age, there may be virtually no stratum corneum.43 This underdeveloped and thin skin structure may be a challenge for clinicians as they attempt to stage a PI. Stratum corneum maturity depends on the gestational age of the neonate, but it is believed to be mature by 30 to 32 weeks' gestational age.45,46 Based on their research, Kalia and colleagues45 found that the state and rate of barrier function development of the stratum corneum are dependent on a combination of gestational and postnatal age.


The stratum corneum controls the loss of evaporative heat and transepidermal water loss (TEWL), which is an important consideration when caring for preterm infants because it is an indicator for skin barrier function.47 Normal adult TEWL levels are less than 10 g/m2 per hour;48,49 this is the same for a more mature infant (>=37 weeks old).46,49 However, in younger infants (<=32 weeks old), this value is higher than 10 g/m2 per hour until maturity is reached.45,46,50 For clinicians, a higher TEWL presents challenges for fluid balance and temperature control because of high insensible water loss; this may translate to dehydration and heat loss.46,47,51 In particular, dehydrated skin, which is dry and lacks the protective moisture that makes skin more resistant to trauma, is more predisposed to skin injuries.


Further, Lund and colleagues50 found that adhesive materials, particularly the removal of adhesive materials, can increase TEWL in neonates. Great care should be taken by clinicians when removing these products or applying products with strong adhesive properties (eg, cloth tape, transparent films). In addition, products that promote adhesion (eg, tincture of benzoin) may result in increased epidermal stripping because of the very strong bond created between a product and the skin.50


Other conditions predisposing premature skin to injury include the diminished cohesion between the epidermis and dermis. In premature infants, the fibrils (rete ridges) that connect the epidermis to the dermis at the dermoepidermal junction are widely spaced and fewer. Although this bond becomes stronger with advancing gestational and postnatal age, until maturity is reached, the neonate is susceptible to injury from adhesive removal, blistering from friction damage, and/or thermal injury.43


Toxicity may occur in the form of topical agents applied to the skin, which may be too readily absorbed. Certain agents have been known to cause issues, including iodine;44,51,52 isopropyl, ethyl, and methyl alcohol;44,53 chlorhexidine;44 and hydrocortisone.54 If antiseptics are used, they should be in an aqueous form rather than a spirit form.44,46 In addition, the use of invasive procedures (eg, intravenous infusions) and adhesives that can cause skin trauma (eg, skin stripping) may further compound toxicity or exacerbate skin damage and increase dryness because they interfere with skin barrier function.44,46,48,55 Preferred barrier products generally are those with a petrolatum base.44 The message for clinicians is protect neonates against toxicity, infection, injuries, and pressure until the stratum corneum has reached maturity.


Edema may be seen in the neonate because there is less collagen and fewer elastic fibers in the dermis.43,44 Edema affects the skin's turgor or elasticity and reduces blood flow, which can result in ischemic injury.43 For clinicians, edema is a signal to protect premature infants from pressure damage using appropriate preventive strategies.


Another important feature of the skin is the acid mantle, a slightly acidic film on the skin's surface. The acid mantle provides protection against some microorganisms and is ideal when the skin surface pH is between 4 and 6.5.43,44,48,49,56 Skin barrier function is altered when the pH shifts from acidic to neutral, which can increase the total number of bacteria or conditions, such as inflammatory dermatoses ("diaper dermatitis").43,57 A more alkaline environment can also increase the TEWL. Full-term infants at birth have a more alkaline skin pH, which drops to a more acidic level like that of adults within days of birth,39,43,49 but this continues to change during the first few weeks of life.57 Fluhr and colleagues57 found the greatest mean skin surface pH on newborns was 6. Earlier work conducted by Fox and colleagues58 on very low birth weight (VLBW) infants found the development of the mantle over time was influenced by birth weight, skin area, and postnatal age. Like term infants, VLBW infants are born with a higher pH that rapidly decreases over the first week and then more gradually over the following 3 weeks.


As children age, issues can occur because of an overall developmental growth issue, such as a larger occipital size versus older children, who are likely to develop a PI in the same areas as an adult (sacrum, heels, etc). The anatomical structure of a young child's head is proportionally larger and heavier, with a lack of adipose tissue. As a result, the occiput is a frequently reported location for PI among younger patients (infants to age 5 years).12,19,30,59,60 Along with anatomic issues, children younger than 5 years cannot properly differentiate pressure sensation from other sensory perceptions such as devices because of their developmental status.15


In summary, because the epidermal layer is thinner and functionally immature and young skin carries a high risk for excess water loss and a higher permeability to chemicals, the prevention of pressure damage and the need for optimal skin care in this group are paramount.21 If the skin's main function is to serve as a barrier to the outside environment, then prevention strategies are important to protect the skin from damage when it is still developing.



The shortcomings of PI risk assessment by bedside nurses specifically may be attributable to multiple factors. These include the lack of validated risk assessment instruments or instruments that can capture all risk factors,20,21,25,26,29,30,61-65 minimal nursing knowledge of neonatal and pediatric integumentary structure and susceptibility to pressure,29,66-68 inadequate nursing knowledge in PI identification and staging, and the dearth of skin bundles specific to pediatric patients.1 However, there are several system and facility barriers to adequate pediatric PI risk assessments as well.


Clinical practice guidelines, to this point, have primarily focused on adult PI prevention practice and treatment. The NPUAP, EPUAP, and PPPIA acknowledged this gap and included a chapter on pediatrics in the 2014 Clinical Practice Guideline.5 Many adult PI research findings cannot be applied to the pediatric population directly because of the anatomic and physiologic differences previously described. Yet there are far fewer PI studies conducted in pediatric populations. This research dilemma is compounded further by the ethical and legal issues involved in carrying out research on a pediatric/neonatal population. The end result has been that clinicians find themselves without evidence from which to determine risk or develop evidence-based interventions. Numerous articles note that it is not unusual for skin care regimens to be based on individual or institutional preference and routine.30,69 This general lack of a unified pediatric protocol structure for PI risk assessments on admission and at regular intervals during hospitalization has led to a varied range of reported pediatric PI data.


Risk Assessment Scales and Psychometric Testing

In 2013, Kottner and colleagues70 published their systematic review of articles addressing pediatric PI risk assessment scales and reported that, of 1,141 articles, only 12 described standardized PI scales for children. They determined that none of the scales that had undergone psychometric testing were superior to another, albeit based on "sparse results." Although there have been many assessments of pediatric skin, skin condition, wound, PI risk assessment instruments, or structured protocols created over the years (Table 2), only a limited number have undergone more serious psychometric testing (Table 3), even since Kottner and colleagues' review. The following paragraphs highlight the pediatric PI risk assessment instruments that have undergone initial psychometric testing.


The Neonatal Skin Risk Assessment Scale, first published in 1997, was developed by Huffines and Logsdon35 specifically for the neonatal population (gestational age 26-40 weeks) at risk of injury and is based off of the Braden scale. It has six subscales: general physical condition, mental status, mobility, activity, nutrition, and moisture. Interrater reliability for the subscales general physical condition, activity, and nutrition was 97%.35 The three subscales that were not included for the pilot study because of low reliability coefficients were mental status, mobility, and moisture. Evidence for predictive validity was present using a cutoff score of 5 with a sensitivity of 83% and specificity of 81%. However, despite the low reliability of the three subscales Huffines and Lodgson35 suggested using all six subscales of the instrument because all are considered important in determining neonate risk.


The Braden Q scale was adapted from the adult Braden Risk Assessment scale in 1996. In 2003, Curley and colleagues71 published their reexamination of the scale's predictive validity and critical cutoff point for classifying risk. The Braden Q scale has the same six subscales as the Braden scale, with an added seventh subscale: tissue perfusion and oxygenation. The seventh subscale was added to reflect unique pediatric developmental characteristics and optimize the benefits of data that are commonly available in PICUs.72 The Braden Q scale is intended for use on pediatric patients from 21 days to 8 years old. Curley and colleagues71 reported a sensitivity of 88% and specificity of 58%; with an at-risk score of 16, high-risk patients will not be missed, nor will preventive therapies be applied on those who do not develop PIs.


The Glamorgan scale73 was the first widely used risk assessment scale to include devices. Willock and colleagues73 published their examination of the scale in 2009. They found that at a risk score of 10, sensitivity was 100% and specificity was 50.2%; at a risk score of 15, sensitivity was 98.4% and specificity was 67.4%; and at a risk score of 20, sensitivity was 93.4% and specificity was 71.5%.73


In 2015, Sterken and colleagues74 published their Pediatric Pressure Ulcer Prediction & Evaluation Tool (PPUPET). On admission, the PPUPET, which also has a subscale for external devices, was found to have a sensitivity of 74.58% and a specificity of 57.94%, retrospectively. On discharge, the PPUPET had a sensitivity of 76.27% and a specificity of 75.70%. However, sensitivity could not be calculated prospectively because of lack of patients with PIs; further, the specificity was very low. The authors believe the latter may be caused by the PPUPET's definition of risk.74


The electronic Skin Injury Risk Assessment + Prevention instrument was published in 2017 by Foster and colleagues75 and also includes external devices. The authors used the Braden and Braden Q as a framework, but modified the eight subscales to have two responses that were "scored" either at risk or not at risk. The foundational concept of this instrument is that if a patient is at risk for any subscale, then the patient is at risk for all subscales. When "at risk" is selected, a list of evidence-based interventions is provided. The authors have compared the reliability and validity to the Braden and Braden Q; the Skin Injury Risk Assessment + Prevention has a correlative reliability of 0.556 and correlative validity range of -0.778 to -0.634.


The newest of these instruments, the Braden QD, was introduced by Curley and colleagues2 in their 2018 publication and was founded on the Braden Q scale. Intended for those patients born preterm to 21 years, the Braden QD scale examines the five subscales of the Braden Q with the addition of two others: number of medical devices and repositionability/skin protection. A total score of 13 or higher indicates that the patient is at risk, with a sensitivity of 0.86 and a specificity of 0.59.


Performing a PI risk assessment is still a valuable method for PI prevention. The 2014 NPUAP, EPUAP, PPPIA International Guideline5 recommended that a structured risk assessment be conducted as soon as possible upon admission (up to a maximum of 8 hours after admission), as often as required by the patient's acuity, and with any significant change to the patient's condition. The admission assessment should include both a risk assessment (to evaluate risk for developing a PI) and a skin assessment (to detect existing PIs). These two assessments should be thought of as a single process step: a PI admission assessment.76


Risk Assessment Instrument Factors and Subscales

The authors' review of literature identified 18 skin and PI risk assessment instruments, some of which have undergone psychometric testing. In these 18 instruments, 58 different factors were identified. This variation and the sheer number of factors support the historic practice of each facility and/or nurse using clinical judgment to prevent pressure or skin injuries at a point in time. Although this may have served many patients successfully, it does leave a potential gap in practice. Any tenured nurse has a wealth of knowledge that cannot be immediately conveyed to newly graduated nurses during preceptorship. However, a risk assessment instrument has the sole purpose of presenting evidence-based practice in an algorithm that results in PI prevention through subscale intervention.


The most common factors in each instrument were the same as items normally found in adult risk assessment tools (Table 4). Nutrition was assessed in 12 (67%) of the 18 instruments, and weight was assessed in 6 (33%). These are important factors in PI prevention, but not all instruments assessed either or both of these factors. Tissue perfusion and skin moisture were each assessed in eight instruments (44%). One would expect that all 18 instruments would have looked at these important subscale factors. More surprisingly, only seven instruments (39%) assessed sensory perception, medical device/cast/splints, or friction/shear factors. However, as expected, mobility/activity was included in 14 (78%) of the 18 instruments. Again, with an effective and comprehensive risk assessment instrument, factors leading to pediatric PI are better understood and identified so that interventions can be put in place for prevention.


In addition, some instruments60,71,74,77 have subscales that measure the concept of shear, which can be an underlying causal factor in PI development. However, this concept has many definitions; risk assessment instruments that claim to measure the concept of shear may in fact be measuring friction, shear force, shear strain, shear stress, or other indirect factors that may not specifically measure all or any components of shear.78 A dedicated exploration of the complex concept of shear is beyond the scope of this article. The authors suggest that the evolution of science regarding shear should be taken into account in the development of future risk assessment scales, and researchers should clearly identify which aspect applies to a given risk assessment score. The forthcoming 2019 NPUAP, EPUAP, PPPIA International Guideline will discuss shear and tissue deformation in detail.


Clinical knowledge and practice have advanced since the first risk assessment instrument was developed. It is imperative that instruments be regularly reviewed against the current science of PI development and validated by reporting reliability, sensitivity, specificity, and predictive values. These instruments are a means for common communication and practice among direct care providers to protect pediatric patients. Initiating PI prevention strategies for at-risk patients, rather than all patients, will optimize the appropriate use of resources.72



Given the complexity of pediatric medicine, there are noted challenges in preventing PIs in this population. Most pediatric prevention protocols have been extrapolated from adult practice because the empiric data on which to base clinical practice guidelines are scarce, particularly for infants.79 Providers should not treat children simply as scaled-down adults;80 as previously discussed, pediatric PIs can be inherently different in etiology. Despite the many challenges, there are many opportunities to implement evidence-based recommendations.


Prevention Strategies for Optimal Skin Health

As previously discussed, maintaining skin integrity, especially in younger pediatric populations, is important in preventing PIs. Avoiding excess moisture is critical, because skin is susceptible to injury not only from moisture, but also the chemicals found in moisture sources such as stool, urine, respiratory devices, and caustic gastrointestinal effluent (eg, tube leakage). The fragility of the skin and the increased PI risk when the skin is damaged require products that can prevent, absorb, and/or diminish further damage. Routine use of petroleum-based products or products with zinc oxide is recommended for dermatitis, as well as "crusting" techniques using stoma powder in combination with a skin ointment barrier. Caustic effluent from a percutaneous endoscopic gastrostomy tube may require the use of a foam dressing for protection and absorption. The most common dressings in pediatric PI management include hydrocolloids, hydrogels (available as amorphous gel and sheets), polyurethane foams, and transparent films.81 Exercise caution with dressings that can trap moisture and cause epidermal stripping, such as hydrocolloids and transparent films. Gentle dressings or adhesives (eg, tapes) with silicone are generally recommended.


Preventing Medical Device-Related Pressure Injuries

With the recent acknowledgement of increasing medical device-related PIs (MDRPIs) among pediatric patients,82,83 more attention has been paid to ill-fitting medical devices or equipment that were not designed for pediatric patients, especially respiratory devices such as tracheostomies, endotracheal tubing, and continuous positive airway pressure (CPAP) machines.25,30,35,36,46,83-85 Interestingly, it appears that various terms other than PI, including "injuries," "necrosis," breakdown," or "trauma," have been used over the years to describe the damage created by respiratory devices that may now be called MDRPI.


For example, Robertson and colleagues86 reported nasal deformities along with "snubbing," "flaring," and columella nasi necrosis from CPAP prongs. Buettiker et al82 performed a randomized study among three different CPAP systems: one nasopharyngeal tube and two types of prong systems. They found that the prong systems caused more "nasal injuries." Yong and colleagues87 randomized different CPAP systems on 89 VLBW infants. One system was a nasal CPAP (N-CPAP) mask, and the other was a nasal prong device. A higher incidence of nasal "trauma" was seen in the nasal prong group. The most common "traumatized" sites were at the nasal septum/philtrum junction for the mask group and the nasal septum walls in the prong group. Further, an integrative review of skin "breakdown" in preterm infants performed by Newnam and colleagues64 identified factors associated with "skin injury" during N-CPAP. A total of 46 studies were selected for data extraction on frequency of occurrence, severity, location, and type of "skin injuries" associated with nasal device interface.64


Because devices are a risk factor for pediatric PI, prevention strategies should aim to mitigate their effect.34 The 2014 NPUAP, EPUAP, PPPIA International Guideline5 made recommendations for reducing MDRPIs in conjunction with clinical judgment based on the patient's clinical situation and goals of care. While there are 19 recommendations for avoiding MDPRIs, the essence of these recommendations is to select and properly fit the medical device; assess the area around and under the device at least twice daily or as needed; and rotate, remove, relieve, or replace the device as necessary. The 2014 NPUAP, EPUAP, PPPIA International Guideline5 recommendations have been upheld as the national standard and adopted by facilities and governing organizations. Adaptation of these recommendations can be seen in the literature; for example, using a moisture- and pressure-redistribution dressing such as a foam dressing83 at the device interface81 to reduce tracheostomy-related PIs. The forthcoming 2019 NPUAP, EPUAP, PPPIA International Guideline will incorporate new evidence regarding the prevention of MDPRI for all populations including children.


Support Surfaces

Based on the patient's identified risk, it is important that prevention strategies such as turning and repositioning are implemented. To augment prevention strategies, support surfaces may be employed to alleviate poor tissue tolerance and shear, improve microclimate, and/or address pain but should not take the place of turning and repositioning.5 Choosing support surfaces for the pediatric population requires critical thinking and understanding of the anatomy and physiology. Pediatric muscle and fat tissue structures are softer than those of adults, making newborns and young children more susceptible to deformation-related injuries.79 A surface needs to envelop the patient to redistribute the pressure, provide a low-friction interface to reduce shear, accommodate the patient's mobility status, and be appropriate for the developmental age of the patient.5,88 Providers should take into consideration the frequent movements and growth requirements of pediatric patients. Further, a support surface should conform to the misplacement of tubes and lines and decrease PI susceptibility.


Computer simulations indicate that air cell mattresses provide superior protection against increased soft tissue deformation around a misplaced tube in NICU and PICU populations, compared with foam mattresses.79,88 Other manufacturers produce low air-loss options such as mattress replacements, overlays, or pads. Unfortunately, the most common products for pressure redistribution, and the research behind them, are geared toward the adult population. The 2014 NPUAP, EPUAP, PPPIA International Guideline5 not only provided general recommendations for selecting a support surface based on mobility level; controlling microclimate; shear reduction; risk of developing PIs; and the number, severity, and location of existing PIs for the adult population, but also recommendations for pediatric patients (under Special Populations: Pediatrics) when selecting support surfaces and repositioning while on a surface.


Prevention by Age Range

Extant literature15 recommends that PI prevention in the pediatric population be conceptualized according to age. Some research has tried to demonstrate the effectiveness of interventions specifically based on age. There appears to be a natural division for care pathways and overall approach to care when guided by a framework based on selection of some defined age range according to characteristics such as integumentary development.


One such example is the neonate's skin immaturity and propensity to PIs and other skin injuries. Based on their findings of extremely low birth weight as a risk factor for nasal trauma, Chen and colleagues89 advocated for guideline development around gestational age and birth weight because of physiologic differences. A multisite prospective study in Japan on PIs in a neonatal population (N = 211) demonstrated that skin texture was a predictor of PI risk.26 Early work by Harpin and Rutter46 demonstrated differences in the effectiveness of skin barrier properties explained by physiologic development of skin structure according to age. Infants who were 32 gestational weeks or less had marked drug absorption and water loss until 2 weeks of age compared with infants born at 37 or more gestational weeks. Newnam and colleagues64 found that neonates of smaller birth weights and younger gestational ages were at risk during N-CPAP use and recommended prevention strategies including frequent skin assessments, focused examinations, correct prong size, adequate humidification, strategies for positioning, and the use of skin barriers to protect them from direct pressure. The authors noted that many of the "injuries" were preventable but that a lack of standardization made prevention difficult, especially in preterm infants.64


In their retrospective study, Schluer and colleagues15 identified factors associated with the development of occipital PIs in pediatric populations. They concluded that their data support early prediction and intervention to prevent PIs according to age.15 In Switzerland, Schluer and colleagues16 conducted a descriptive, multicenter point prevalence study on 412 patients from birth to 17 years. They found that the age and the department/unit were the two single characteristics that influenced PI occurrence, stages 2 to 4. Patients with PI stages 2, 3, and 4 were older than 8 years and had chronic conditions or surgical procedures, especially orthopedics. One case-control study (N = 59) in a 30-bed PICU found that the majority of PIs developed in infants younger than 3 years.90 Distribution of PIs in patients younger than 1 year was 36%, whereas patients between 1 and 3 years had 30% of the PIs.


Based on literature like this, it seems evident that age-appropriate ranges are one way to categorize prevention strategies. However, part of the problem in addressing PI prevention by age may be that extant prevalence data may not include all pediatric-age groups or individuals, and thus epidemiologic data may not be reflective of pediatric populations at large. Further, to date, the literature demonstrates differences among pediatric populations regarding risk factors and PI locations.91 More research is required to identify whether these differences truly lead to an increase in PIs and thus require prevention strategies according to age group. Regardless, an argument may be made for the allocation of intervention bundles according to specific age ranges to allow for individualized care.


Prevention Bundles and Programs

Empiric evidence has shown that multicomponent interventions may be more effective than individual actions in the prevention of PIs.92 Pre- and postintervention studies, framed as quality improvement, describe interprofessional and multifaceted intervention bundles that have successfully decreased PI prevalence and incidence in specific populations.20


Solutions for Patient Safety, an initiative designed to reduce occurrences of harm in pediatric hospitals, examined active participation in a collaborative to implement PI prevention bundles of nursing interventions and found that PI occurrence decreased by 57%.93 Implemented from 2009 to 2016, the bundles included five risk factors: medical devices, moisture, immobility, skin integrity, and support surface selection. No particular risk factor exerted a greater effect on PI occurrence, supporting the need for intervention bundles.


Frank and colleagues1 also studied the pediatric population in 33 hospitals that were members of the Solutions for Patient Safety initiative. Their objectives were twofold: to increase the detection of PIs through active surveillance and to reduce the number of serious PIs (stage 3, stage 4, unstageable, deep tissue PI). This project used a three-pronged approach consisting of active surveillance, a prevention bundle, and the deployment of a wound ostomy continence nurse. After the implementation of the bundle, they found a decrease in PIs: 0.06 to 0.03 per 1,000 patient-days in participating institutions. They also found that hospitals reporting greater than 80% bundle adherence reported fewer PIs. Using a patient/day formula, Visscher and colleagues20 found that PICU PIs decreased from 14.3 to 3.7/1000 patient-days after implementing a quality improvement bundle. In the NICU, however, they found that PIs did not significantly change after bundle implementation.


In a children's hospital, Boesch and colleagues94 noted a high number of tracheostomy-related PIs in their ventilator unit and implemented a bundled intervention model that included reducing moisture and pressure at the device interface. They implemented the model over a 30-month period and found a decrease in the number of patients who developed a tracheostomy-related PI, from 8.1% to 2.6%. With the intent to improve quality of care and decrease incidence of nasal trauma, Chen and colleagues89 initiated a standardized process and protocol with prepackaged kits. The kits and standardized nursing protocol decreased the incidence of nasal trauma from 42.2% to 19.6%, except for infants with extremely low birth weight (less than 1,000 g). The authors concluded that preventing nasal trauma by implementation of standard nursing protocol during N-CPAP is potentially one of the greatest opportunities for preventing of skin injury in this patient population.


In a PICU of a large tertiary care center, a prospective, quasi-experimental study was conducted to determine if a PI prevention program reduced PI development.21 The program included a skin care bundle that incorporated five components: appropriate support surface, frequent turning and repositioning, moisture and incontinence management, appropriate nutrition, and nursing staff education. The staff in the control group received education, and the patients received standard care. The intervention group also received education and standard care, but incorporated skin care champions (staff nurses) who helped to facilitate adherence to the bundle and unit-based advanced practice nurses who performed root-cause analyses. A [chi]2 analysis revealed that PI development in the control group was significantly higher than in the experimental group. This study demonstrates the importance of a systems approach to bundled interventions, along with dedicated skin care champions who reinforce and implement change into daily practice.


Prevention Through Industry Partnerships

Taking into consideration pediatric vulnerability to PIs and the current standard of care, several implications become apparent for the future of informed clinical practice. For example, given the high occurrence of MDRPIs, collaboration with industry partners to develop innovative solutions is one way to attack the root cause of PIs. The recommendations of Robertson and colleagues86 on pediatric CPAP use included providing rest time and ensuring an appropriate fit, but more importantly, they reported working with the manufacturer to address design flaws. The study led to a collaborative effort with the manufacturer to develop a new curved design with tapering nasal prongs that would help to eliminate the issues. In addition, the manufacturer worked with staff on modifications and learning activities that would support care until the new design was available. This is an example of a positive and productive resolution arising from a collaborative effort between clinicians and a manufacturer.


In their integrative literature review, Newnam and colleagues64 found that researchers had recommended device design changes that would ultimately reduce tissue injury. A retrospective chart analysis of occipital PI incidence found that the majority of patients younger than 1 year were critically ill and using multiple medical devices,59 including endotracheal tubes, mechanical ventilation, extracorporeal membrane oxygenation, central venous catheters, nasogastric tubes, saturation probes, and electroencephalography leads. This finding demonstrates the imperative to collaborate with industry partners to minimize the risks associated with these medical devices.


In their secondary analysis of the National Database of Nursing Quality Indicators, Razmus and Bergquist-Beringer95 found that pressure redistribution support surface use as an intervention in the pediatric population was lower than in a previously reported adult population. Based on this finding, they recommended further investigation to better understand the effectiveness of support surface use in decreasing pediatric HAPIs. What was not clear to them was whether the pressure redistribution support surfaces were designed for pediatric or adult patients.


Clearly, end users of a product are in a position to offer recommendations and suggestions for innovative designs based on daily clinical experience. All clinical disciplines offer value when consulting with industry members involved in the research and design of equipment and devices that address the unique aspects and needs of a special population, such as anatomical or care needs.


There are various opportunities to partner with industry and manufacturers to improve the design, safety, and efficacy of devices, especially in the pediatric population.96 Clinicians can partake in these opportunities through product evaluation committees in their own institutions or participate for advisory boards that engage clinicians and researchers for new product development; in fact, the American Nurses Association works to promote nurses who serve on various types of advisory boards through their Nurses on Boards Coalition.97 The NPUAP, which is composed of medical, nursing, physical therapy, nutrition, and industry stakeholders, forms a cohesive partnership with a mission to serve as the authoritative voice for improved patient outcomes in PI prevention and treatment through public policy, education, and research.98 This includes the Support Surface Standards Initiative (overseen by the NPUAP Research Committee), which is an interprofessional mix of industry, researchers, academics, and practicing clinicians who work together to standardize support surface performance evaluations.99


To be clinically relevant and meet the needs of the pediatric population, collaboration is required between professional caregivers and those involved in the design and development of equipment and medical devices. Developing devices and equipment that achieve highly reliable and quality care through the partnership of industry, researchers, academics, and providers should be the norm. Such interprofessional teams achieve the synergy required to enhance products and ultimately care.


Opportunities for PI Treatment

Unfortunately, like prevention strategies, pediatric PI treatment protocols are extrapolated from adult practice because of the paucity of relevant empiric data on which to base guidelines for clinical practice, particularly in infants.79 Pediatric wound management lacks consensus because research is geared toward adults, which can pose risks to the neonatal and pediatric populations. Baharestani and Ratliff30 stated that the rapid, uncomplicated wound healing of pediatric patients gives rise to a limited need for intervention, making it the "normative expectation" in this population. Some providers believe that healing occurs more expeditiously in younger patients, which is one of several factors that have resulted in\ the lack of consideration for wound care protocols with these populations.30


Wound care practices are currently based on a combination of provider experience and preference as well as a small number of published clinical guidelines based on expert opinion. This includes the choice of specific dressings or other wound care products for pediatric populations as evidenced by the following examples. Transparent films and hydrocolloids were favored at one point, especially in the younger pediatric populations. However, their increased propensity to cause skin stripping and/or moisture-associated skin damage has caused them to fall out of favor.44,48,55,81,100 Medical-grade honey has been used more recently because it is seen as a "natural" product and parents and children respond positively to natural and gentle dressings that are effective and easy to use.81,101 There is also documentation regarding its efficacy in healing wounds in pediatric populations, particularly oncology patients.81,101-103


However, rigorous evidence-based criteria and clinical guidelines for wound management for these populations are limited at best.81 Unfortunately, because of the lack of clear-cut treatment guidance, several problems arise. Importantly, clinicians may have to balance manufacturer-recommended products (which may not have been created with the pediatric patient in mind) with clinical concerns such as skin immaturity and absorption issues.30 Given these issues, clinicians often find it difficult to determine the appropriate treatment.


The future of wound management for neonates and other pediatric populations will depend on continued research and guidelines created to assist clinicians in treating PIs. Currently, there are only a limited number of published clinical guidelines for the evaluation and management of wounds in neonatal and pediatric populations. None of these have undergone the rigorous assessment required for the generation of evidence-based guidelines.81



This white paper reviewed the history of and continued journey to pediatric PI prevention to reveal the scope of the problem, how pediatric anatomy and physiology can lead to PI formation, and the current recommendations for pediatric PI prevention and treatment. More recent published literature and trends show that clinicians are paying attention to the specific issues that make this population vulnerable to PI formation. This population requires special consideration, protocols, and approaches compared with adult or other specific populations. The slow but steady realization of this fact has significantly advanced provider thought processes, approaches, and care provisions particularly when addressing PI prevention and treatment. The wound care discipline must construct standardized approaches that involve targeted risk assessment, evidence-based guidelines, prevention strategies, medical equipment and device design, and wound treatments specific to this special and vulnerable population. This can only be accomplished by working in interprofessional teams that integrate all stakeholders, including industry partners.




* Pediatric patients, especially neonates and infants, are vulnerable to PI formation.


* Pediatric patients should have a risk assessment using a validated risk assessment instrument for successful PI prevention.


* The known PI prevention principles are appropriate for the pediatric population, but the implementation is slightly different for each developmental age.


* There are limited evidence-based guidelines for treatment and management of pediatric PI.


* Providers must work in interprofessional teams that integrate all stakeholders, including industry partners, to effectively prevent and treat pediatric PI.




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