What is Underpad chux: Uses, Safety, Operation, and top Manufacturers!

Introduction

Underpad chux are absorbent protective pads placed under a patient to help contain and manage unwanted fluids (for example, urine, stool, wound drainage, or procedural fluids) and to protect hospital surfaces such as mattresses, stretchers, procedure tables, wheelchairs, and chairs. They sit at the intersection of patient comfort, skin protection, infection prevention, and operational efficiency—especially in busy acute care units, long-term care environments, and ambulatory settings.

In many facilities, the word “chux” is used generically (similar to how some brand names become everyday terms) to refer to an underpad, regardless of the actual manufacturer. You may also hear terms like inco pad, blue pad, bed protector, or disposable underpad. Despite the informal terminology, the product’s design details matter: two products that look similar can behave very differently in absorption speed, leakage resistance, and skin comfort.

Although Underpad chux are not “high-tech,” they are still widely used hospital equipment and, in many jurisdictions, may be regulated or treated like a medical device or medical accessory. Selection, correct use, and disposal practices can materially affect linen costs, bed turnaround time, staff workload, exposure risk, and patient experience.

Underpad chux also have a measurable operational footprint: they are bulky to store, frequently moved through the supply chain, and can meaningfully affect waste volumes. For that reason, many organizations evaluate underpads not only on unit price, but also on total cost of ownership (laundry savings, environmental services labor, mattress protection, and waste handling).

This article provides general, non-medical, globally relevant guidance on what Underpad chux are, when they are typically used, how to use them safely, how to think about performance (“output”), how to troubleshoot common issues, and how the global market differs by country for procurement and supply planning. It is not clinical advice and is not a substitute for facility policies, local regulations, or manufacturer instructions for use.

What is Underpad chux and why do we use it?

Clear definition and purpose

Underpad chux (often referred to as underpads, absorbent bed pads, or incontinence underpads) are single-use or reusable pads designed to:

  • Absorb fluid quickly into an internal core
  • Reduce “strike-through” (fluid reaching the top surface after initial absorption)
  • Prevent leakage to the surface beneath using a liquid-resistant or waterproof backing
  • Provide a barrier between the patient and hospital surfaces

In practical terms, Underpad chux support patient care by keeping surfaces drier and cleaner and by simplifying cleanup when fluid exposure occurs.

A practical way to think about Underpad chux is that they are surface-protection and containment tools. They can support continence care plans and hygiene workflows, but they are not a replacement for primary continence products (briefs, diapers, catheters, or toileting programs) and they are not a substitute for wound dressings. Their value is often highest in the “in-between” moments—during transfers, procedures, waiting periods, or when fluid exposure is unpredictable.

Common design elements (varies by manufacturer)

Most Underpad chux include:

  • Top sheet (patient-facing layer): Often nonwoven and designed to feel soft while allowing fluid to pass through.
  • Absorbent core: Frequently a mix of fluff pulp and superabsorbent polymer (SAP); structure and capacity vary by manufacturer.
  • Back sheet (bottom layer): Typically a fluid-impermeable or fluid-resistant film; some products are marketed as breathable.
  • Sealed edges: To reduce leakage from the sides.
  • Optional features: Wings/tucks, adhesive strips, non-slip backing, wetness indicators, odor-control claims, or quilted channels (all vary by manufacturer).

Because performance is product-specific, procurement teams should rely on manufacturer documentation and internal evaluation rather than assuming equivalence across brands.

Additional design details that often influence real-world performance include:

  • Acquisition / distribution layers: Some pads add an internal “acquisition” layer that pulls liquid away quickly, and a “distribution” layer that spreads fluid across the core to reduce pooling and edge leakage.
  • Core wrap and anti-gel features: SAP can swell into gel; core construction and wrapping may reduce clumping and help keep liquid locked in during movement.
  • Breathability vs. leakage resistance trade-offs: “Breathable” backings may improve heat/moisture comfort for some users, but the actual balance depends on film design and seams. Breathability claims are not standardized across all markets.
  • Noise and handling feel: Film backings can be “crinkly” and may affect patient comfort or perceived quality, especially in long-term care.
  • Lint and fiber shedding: In some environments (imaging suites, neonatal areas, or procedure rooms), linting can be a practical concern even when infection risk is low.
  • Reusable underpads: Reusable products (where used) typically rely on layered textiles and a waterproof/breathable membrane. They require laundering, inspection, and lifecycle tracking, but can reduce solid waste.

Common clinical settings

Underpad chux are used across many care environments, including:

  • Acute inpatient wards (medicine, surgery, orthopedics)
  • ICU/critical care (high frequency of lines, drains, and fluid exposure)
  • Emergency departments (rapid turnover, uncertain patient needs)
  • Long-term care and rehabilitation
  • Labor and delivery/postpartum areas
  • Dialysis units
  • Outpatient clinics and ambulatory procedure areas
  • Radiology and transport (stretcher protection and contamination control)

They are also used outside hospitals (home care, assisted living), but this article focuses on institutional and organized-care use cases.

In many institutions, Underpad chux are also routinely found in:

  • Pre-op holding and post-anesthesia care areas (PACU): Where nausea/vomiting risk and wound drainage may be higher.
  • Endoscopy and minor procedure rooms: As a non-sterile protective layer under patients during preparation and recovery (sterile drapes still apply when needed).
  • Oncology infusion and outpatient treatment chairs: To protect upholstery during long sessions where continence risk or spill risk exists.
  • Palliative and comfort-care settings: Where the emphasis is on dignity, rapid cleanup, and minimizing unnecessary linen changes.
  • Specialty clinics (urology, geriatrics, neurology): Where continence-related workflows are frequent.
  • Ambulance bay / patient transfer points: Particularly when stretchers move between departments and contamination control is a priority.

Key benefits in patient care and workflow

When implemented within facility protocols, Underpad chux can offer:

  • Surface protection: Reduced contamination of mattresses and equipment upholstery.
  • Operational efficiency: Faster changeover of beds, chairs, and stretchers compared with full linen changes in some scenarios.
  • Staff safety: Less direct contact with contaminated fluids when removal and disposal are done correctly.
  • Patient dignity and comfort: Reduced visible soiling and less time waiting for bed changes.
  • Cost control (context-dependent): Potential reductions in laundry volume, mattress cover damage, and environmental cleaning labor—balanced against consumable spend and waste disposal costs.

Additional operational and quality benefits often cited by facilities include:

  • Protection of high-cost assets: Mattress covers, specialty support surfaces, and transport equipment can be expensive to repair/replace. Even small reductions in contamination events can have outsized cost impact.
  • Support for standardized rounding workflows: When pad checks and changes are integrated into routine care rounds, tasks become more predictable and less “urgent cleanup.”
  • Reduction of cross-area contamination: A controlled “remove–contain–dispose–clean” sequence can reduce tracking of fluids to bed rails, floors, and staff clothing.
  • More reliable bed turnover: Underpads can reduce the frequency of “unexpected mattress contamination” events that delay admissions or transfers.

When should I use Underpad chux (and when should I not)?

Appropriate use cases

Underpad chux are typically used when there is a reasonable expectation of fluid exposure to a surface. Common examples include:

  • Incontinence management support: Episodes of urinary or fecal incontinence, or suspected leakage around continence products.
  • Catheter-related leakage protection: Protection of linen and mattress surfaces when leakage is anticipated (usage and monitoring follow facility protocols).
  • Wound and drain protection: Containing expected drainage during dressing changes or if a drain is leaking (not a substitute for appropriate dressings).
  • Procedural and hygiene care: Bed baths, perineal care, oral care, emesis risk situations, and minor bedside procedures where fluid may drip or spill.
  • Transport and waiting areas: Protection of stretchers and wheelchairs during transfers and while waiting for imaging or treatment.
  • Isolation workflows: As part of surface protection and contamination control in rooms with higher bioburden risk (as directed by infection prevention policies).

For operations leaders, the most efficient use is usually targeted: placing Underpad chux only where fluid exposure is likely, and removing them promptly when soiled.

Other common, practical scenarios where facilities may use Underpad chux (subject to local protocols) include:

  • Postpartum care: Managing lochia and protecting bedding during early recovery, particularly during transfers and early mobilization.
  • Bowel preparation and GI symptoms: When diarrhea risk is elevated, pads can help protect surfaces during episodes while hygiene care is organized.
  • Emesis-prone situations: Recovery from anesthesia, motion sickness during transport, or acute illness where vomiting is possible.
  • Line and access site protection during care: For example, during removal of dressings or flushing of lines where small fluid spills can occur (the pad is for surface protection, not sterility).
  • High-perspiration or fever episodes: When moisture management is needed to protect linens and reduce frequent full bed changes.
  • Chair protection during long sittings: Rehabilitation or dialysis chairs may need targeted pads to protect upholstery while preserving patient comfort.

Situations where it may not be suitable

Underpad chux may be a poor choice—or require extra controls—in the following situations:

  • As a lifting or transfer aid: Underpad chux are not designed as slide sheets or lifting slings; tearing and patient injury risks increase when used for manual handling.
  • As a substitute for pressure injury prevention measures: Underpad chux are not pressure-redistribution surfaces; excessive layering can increase heat/moisture and reduce mattress performance.
  • Where a sterile field is required: Most Underpad chux are not sterile unless explicitly labeled sterile (varies by manufacturer). Procedure-specific drapes may be required.
  • High-volume fluid procedures: If fluid volumes are high, specialized drapes, suction, or containment systems may be needed; Underpad chux alone may leak or saturate.
  • When product materials are incompatible: Adhesives, backings, or top sheets may interact with certain surfaces or skin protectants. Compatibility varies by manufacturer and facility practice.
  • Imaging considerations: Some pads may be discouraged on certain imaging tables or during specific imaging sequences due to local protocols. Follow radiology department guidance.

Additional “not suitable” or “use with caution” considerations that often come up in practice:

  • Specialty support surfaces: Some advanced mattresses and overlays rely on airflow and microclimate management. Adding non-breathable layers (including some underpads) can reduce intended performance.
  • Bed-exit or sensor systems: In some beds, added layers can affect sensor accuracy or patient positioning. Follow bed manufacturer guidance and facility policy.
  • Behavioral health environments: Tearable materials can become a safety concern in certain supervised settings; facilities may use alternative approved products.
  • When a reusable option is mandated: Some organizations restrict disposables in certain areas for sustainability or waste management reasons, using laundered alternatives with defined handling rules.

Safety cautions and contraindications (general, non-clinical)

  • Do not place Underpad chux on the floor as a spill mat unless specifically allowed by facility policy; it can become a slip hazard.
  • Avoid wrinkles and bunching under the patient, which can contribute to friction and discomfort.
  • Change promptly when soiled to reduce prolonged moisture exposure and odor; timing is defined by clinical protocols.
  • Check for sensitivity to materials (top sheet, adhesives, fragrances, odor-control additives), recognizing that composition varies by manufacturer.
  • Keep packaging intact and dry until use; damaged packaging should be handled according to facility policy.

Additional practical cautions that can prevent avoidable incidents:

  • Avoid trimming or cutting pads unless the manufacturer and facility policy explicitly allow it; cutting can compromise edge seals and increase leakage.
  • Do not apply adhesive strips to skin: Adhesives (if present) are typically intended for linen or mattress covers, and even then only if compatible with the surface.
  • Be cautious around alcohol-based prep solutions and heat sources: Absorbent materials can retain liquids; follow peri-procedural policies regarding drying times, ignition sources, and material placement.
  • Do not “hide” wet pads under layers: If a pad is wet, it should be changed. Covering it with another pad can trap moisture and may worsen skin comfort and odor.

What do I need before starting?

Required setup, environment, and accessories

Before placing Underpad chux, ensure the basics support safe, efficient care:

  • Correct product type: Size and absorbency appropriate to the task (chair vs bed, light vs heavy absorbency), as specified by facility formularies.
  • PPE: Gloves and additional PPE as indicated by standard precautions and isolation requirements.
  • Waste disposal supplies: Appropriate waste bag or bin access based on local waste segregation rules.
  • Supporting materials: Clean linen (if used), skin cleansing supplies, barrier products (if part of protocol), and spare Underpad chux for timely changes.
  • Safe environment: Bed brakes locked, adequate lighting, privacy measures, call bell accessible, and ergonomic access for staff.

Underpad chux are “low equipment,” but the process is safer and faster when supplies are prepared before patient repositioning.

For smoother workflow and fewer interruptions, many units also standardize:

  • A “pad change kit” approach: Pre-staged gloves, wipes, barrier products, and a single standard underpad SKU for the ward (where clinically appropriate).
  • A clean surface or caddy for supplies: Especially in isolation rooms, to avoid placing items on potentially contaminated bedside tables.
  • A plan for linen management: Knowing whether the pad sits over a draw sheet, under a flat sheet, or directly on a mattress cover can reduce confusion during hurried changes.
  • Ergonomic support: For heavier patients or limited-mobility patients, having the right number of staff and approved repositioning aids prevents unsafe “quick pulls.”

Training and competency expectations

Underpad chux placement is commonly delegated, but safe use still benefits from structured competency:

  • Orientation on correct placement (backing down, absorbent side up, center alignment, wings/tucks if present).
  • Manual handling training: Clear guidance that Underpad chux are not transfer devices.
  • Skin integrity awareness: Recognizing moisture/friction risks and how to minimize wrinkling and prolonged dampness.
  • Infection prevention practices: Safe removal, containment, disposal, and environmental cleaning steps.
  • Documentation expectations: What to record (for example, skin checks, pad changes per protocol, or unusual leakage patterns), as defined by the facility.

In many facilities, the most common real-world errors are simple and preventable (pad placed upside down, pad placed too low on the bed, pad not wide enough for patient movement, or staff using the pad to “drag” a patient). Competency programs that include return demonstration and scenario-based practice (bed, chair, transport stretcher) often reduce these errors more effectively than written instructions alone.

Pre-use checks and documentation

A practical pre-use check for Underpad chux includes:

  • Packaging integrity: No tears, punctures, moisture damage, or contamination.
  • Correct SKU: Confirm absorbency level, dimensions, and features (wings, adhesive, wetness indicator) match the intended use.
  • Lot/traceability information: Record when required by policy; this supports complaint handling and recalls.
  • Visible defects: Tears, delamination, damaged backing, or excessive linting.
  • Storage conditions: Pads should be stored clean, dry, and off the floor, following local policy and manufacturer guidance.

Documentation requirements vary significantly by facility, payer, and country. Where auditing is common (for example, pressure injury prevention programs or incontinence care pathways), consistent charting and product standardization reduce variability.

Additional checks that may be relevant in regulated or highly standardized environments:

  • Expiry date (if present): Not all underpads display an expiry date, but where it exists it should be respected, especially for products with adhesives or specialized coatings.
  • Label claims required by policy: For example, latex-free status, fragrance-free status, or “breathable backing” claims.
  • UDI or equivalent identifiers (where applicable): Some jurisdictions require unique device identification for certain product categories; facilities may incorporate this into inventory and traceability workflows.

How do I use it correctly (basic operation)?

Basic step-by-step workflow

The following is a general workflow; always follow your facility protocol and the manufacturer’s instructions for use (IFU):

  1. Prepare the area: Gather Underpad chux, PPE, disposal supplies, and any skin/linen items needed.
  2. Hand hygiene and PPE: Perform hand hygiene and don gloves (and other PPE as required).
  3. Explain and preserve dignity: Provide a brief explanation, ensure privacy, and minimize exposure time according to facility practice.
  4. Remove soiled materials safely: If replacing an existing pad, roll it inward (contaminated side in), contain it, and dispose according to policy.
  5. Inspect surfaces: Check for moisture on the mattress cover or chair surface; clean/disinfect if needed per environmental services protocol.
  6. Select placement location: Typically under the pelvis/hips for incontinence risk, or under the expected fluid source for procedures.
  7. Position Underpad chux correctly:Absorbent side up (patient-facing) – Waterproof or resistant backing down (surface-facing) – Center the pad so the most absorbent area is under the expected fluid exposure zone
  8. Use wings/tucks if present: Tuck under the mattress or secure as designed; do not attach adhesives to skin.
  9. Smooth and flatten: Remove wrinkles and avoid bunching; ensure it does not create ridges under bony prominences.
  10. Reposition the patient safely: Use appropriate transfer equipment and techniques; do not pull on the pad for repositioning unless explicitly allowed by protocol (and even then, verify product strength and method).
  11. Monitor and replace as needed: Check periodically; replace promptly when wet/soiled and document as required.
  12. Dispose and perform hand hygiene: Remove PPE safely and complete hand hygiene.

For immobile patients, many teams use a “fold and roll” placement method (aligned with manual handling policies): the clean pad is folded lengthwise and placed close to the patient’s body during a gentle turn, then rolled flat under the pelvis as the patient is returned to position. This can reduce the need for full lifts and helps maintain correct placement without tugging on the pad as a pulling surface.

For chairs and wheelchairs, additional placement tips include:

  • Ensure the pad is fully supported by the seat (no long overhang) so it doesn’t brush the floor and become contaminated.
  • If the chair has contours or a pressure cushion, choose a pad size that lays flat without creating folds at the edges.
  • If the patient is likely to slide forward, consider non-slip designs or facility-approved securing methods that do not involve skin contact.

Setup, “calibration,” and operation (what’s relevant)

Underpad chux are not electronic clinical devices and do not require calibration. Operational reliability comes from:

  • Correct product selection (absorbency and size)
  • Correct orientation and placement
  • Timely replacement when saturated or soiled
  • Safe disposal and surface cleaning

A useful operational concept for underpads is “right pad, right place, right time.” Many leakage problems are not “bad products” but a mismatch between pad size/absorbency and the reality of patient movement, bed angle, or fluid volume.

Typical “settings” and what they generally mean

Underpad chux often come with product options rather than device settings. Common options include:

  • Absorbency level: Light/moderate/heavy (terminology and capacity vary by manufacturer; there is no universal scale).
  • Dimensions: Bed-size rectangles vs chair-size pads; bariatric sizes may be available.
  • Backing type: Standard waterproof film vs “breathable” backing (performance claims vary).
  • Attachment method: Wings/tucks, adhesives, or non-slip backings (varies by manufacturer).
  • Wetness indicator: A line or pattern that changes appearance when wet (where present, it is a qualitative cue—not a measurement tool).

For procurement teams, these “settings” should be standardized within formularies so staff are not forced to guess which pad fits a scenario.

Other product “options” that can affect bedside experience include:

  • Quilted vs flat construction: Quilting can help distribute fluid and reduce pooling, but construction varies widely.
  • Core material mix: Higher SAP content may improve fluid lock-in, while different pulp structures may affect acquisition speed.
  • Fold pattern and packaging format: Some products are folded to speed placement or reduce storage footprint; others are bulk-packed for cost efficiency.

How do I keep the patient safe?

Safety practices and monitoring

Underpad chux support safety when they are used as a barrier and absorbent layer, not as a substitute for clinical care plans. Key safety practices include:

  • Prevent prolonged dampness: Replace when wet/soiled to reduce extended moisture contact with skin and linen.
  • Minimize friction and shear: Keep the pad flat and avoid wrinkles; reposition patients using approved transfer aids.
  • Support skin integrity protocols: Use facility-approved skin cleansing and barrier approaches; product interaction varies by manufacturer.
  • Protect equipment surfaces appropriately: Ensure the backing faces downward; leakage onto mattress seams or upholstery increases cleaning burden and contamination risk.
  • Avoid over-layering: Multiple pads and linens can trap heat and moisture and may reduce mattress support characteristics; follow local guidance.
  • Maintain dignity and privacy: Efficient changes reduce exposure time and patient distress.

From a non-clinical safety and comfort perspective, it can be helpful to understand the concept of microclimate (heat and moisture at the skin–surface interface). Some underpads, especially those with fully occlusive backings, can trap heat and moisture if left in place too long or layered. This does not mean they are “unsafe,” but it reinforces why timely changes, correct placement, and avoiding unnecessary layers are important.

For high-risk patients (limited mobility, heavy perspiration, frequent incontinence episodes), facilities often coordinate underpad use with:

  • scheduled turning/repositioning routines,
  • routine skin checks per protocol, and
  • targeted moisture management steps approved by the care team.

Alarm handling and human factors (what applies to this product)

Underpad chux typically have no electronic alarms, but human factors still matter:

  • Standardization reduces error: If wards stock too many similar-looking absorbency levels, mis-selection is common.
  • Visual management helps: Clear labeling on storage bins, color coding (where used), and “one ward, one standard” approaches improve consistency.
  • Workflow design prevents missed changes: Define who checks pads, how often, and what triggers a change (policy-driven).
  • Communicate across shifts: Handover should include any recurring leakage patterns or supply constraints.

If wetness indicators are used, they should be treated as an attention cue, not a clinical “alarm.” Indicators can be obscured by linens, and different brands use different visual signals. A clear local rule (for example, “indicator change triggers a check at next round”) prevents inconsistent interpretation.

Additional risk considerations (general)

  • Slips and falls: Wet pads can lead to slippery floors during changes; keep waste contained and clean spills immediately.
  • Allergies/sensitivities: Avoid fragranced or additive-containing products if policy or patient needs require; composition varies by manufacturer.
  • Heat sources and procedures: In procedural areas, follow local policies regarding absorbent materials near heat sources, prep solutions, or electrosurgical workflows.
  • Pediatrics and vulnerable populations: Ensure product size and placement are appropriate; prevent loose pieces becoming a hazard if a pad is torn.

Most facilities treat Underpad chux as simple supplies, but safety improves markedly when they are integrated into skin care, falls prevention, and infection prevention programs.

Additional practical considerations in some environments include:

  • Noise and sleep disruption: Crinkly backings can be noticeable at night; comfort-focused units may prefer softer, quieter constructions.
  • Patient confusion and tampering: Patients with cognitive impairment may pull at pads. Selecting more robust designs and ensuring frequent checks can reduce tearing and contamination.
  • Bariatric care: Larger body habitus and higher movement forces may require wider pads, stronger edge seals, and clear guidance that pads are not repositioning aids.

How do I interpret the output?

Types of outputs/readings (what “output” means here)

Underpad chux do not generate numerical readings like an electronic medical device. The “output” is typically observational:

  • Saturation level: Dry, damp, wet, or soaked appearance/feel.
  • Strike-through: Whether fluid has returned to the top surface after absorption.
  • Leakage: Fluid reaching linen, mattress cover, chair upholstery, or the floor.
  • Wetness indicator changes: If the product includes an indicator (qualitative, not quantitative).
  • Odor and containment: Whether the pad is containing fluid without spreading beyond the intended area.

How clinicians typically interpret them (general)

In routine care, staff may use Underpad chux to support:

  • Timely recognition of wetness (prompting hygiene care per protocol)
  • Surface protection checks (confirming bedding and mattress cover remain clean/dry)
  • Trend awareness (for example, repeated saturation may signal the need to review the overall continence plan—handled by the clinical team)

Importantly, Underpad chux are not designed to measure fluid volume, and they should not be treated as a substitute for defined output measurement methods (which are governed by clinical policy).

From an operations perspective, “interpretation” is often about identifying patterns such as:

  • pads saturating consistently within short intervals,
  • leakage incidents occurring primarily during patient sitting/upright periods,
  • higher failure rates after a product substitution, or
  • higher usage on specific shifts due to workflow or stocking differences.

These patterns can point to training gaps, product mismatch, or supply issues rather than individual staff performance.

Common pitfalls and limitations

  • Mistaking absorbency for measurement: Absorbent capacity is not a calibrated measurement tool.
  • Assuming all pads are equivalent: Absorbency labels are not standardized globally; “heavy” in one brand may differ from another.
  • Ignoring bed angle and patient movement: Upright positioning can drive fluid toward edges and increase leakage risk.
  • Layering masks problems: Stacked pads may hide leakage until it reaches the mattress, complicating cleaning and increasing exposure risk.
  • Over-reliance on odor control claims: Odor-control features (if present) vary by manufacturer and do not replace timely changes and hygiene.

For quality improvement teams, the most actionable “output” metrics are often operational: pad usage rate per patient-day, leak incidents, mattress contamination rates, and linen utilization—measured at the ward or facility level.

A useful addition for procurement discussions is that manufacturers may provide laboratory-style performance data (for example, total absorbency capacity under a specified test method, “rewet” performance, or acquisition time). These figures can be helpful for comparing products, but they still may not predict bedside performance unless the facility tests the pads under realistic conditions (patient movement, bed angles, and typical volumes).

What if something goes wrong?

Troubleshooting checklist

When Underpad chux performance is not meeting expectations, a structured check helps:

  • Leakage at edges
  • Verify the pad is centered under the highest-risk area.
  • Increase size or absorbency level (per formulary).
  • Check if the bed is elevated; consider repositioning or alternate placement.
  • Confirm the backing is facing downward and the edges are not folded up.

  • Strike-through (surface stays wet)

  • Confirm the product is intended for direct skin contact; some pads prioritize surface protection rather than dryness.
  • Replace more frequently in high-output situations.
  • Review whether additional moisture-wicking products are required (policy-driven).

  • Pad sliding or bunching

  • Use wings/tucks or non-slip options if available.
  • Ensure the sheet system and mattress cover are compatible (very slick surfaces increase migration).
  • Avoid using the pad as a repositioning tool.

  • Tearing or delamination

  • Confirm staff are not pulling on the pad during transfers.
  • Inspect storage conditions (heat/humidity can degrade some materials over time; varies by manufacturer).
  • Quarantine visibly defective stock and report through internal quality channels.

  • Skin irritation complaints

  • Assess whether adhesive, top sheet texture, or additives may be contributing (varies by manufacturer).
  • Ensure the pad is changed promptly when wet/soiled.
  • Escalate to the clinical team and follow facility reporting pathways for suspected product-related issues.

Additional troubleshooting issues that frequently appear during product changes or supply disruptions:

  • Unexpected odor despite “odor control”
  • Confirm change frequency and hygiene workflow timing.
  • Check whether pads are being over-layered (trapping moisture).
  • Confirm the pad is stored properly; carton moisture damage can sometimes affect odor and performance.

  • Sudden increase in leaks after a substitution

  • Verify the substitute SKU’s size and absorbency are truly comparable (labels can be misleading).
  • Re-educate staff on identifying the “absorbent side” if the product looks different.
  • Report trends quickly to materials management so substitution decisions can be reviewed.

When to stop use

Stop using a specific Underpad chux item (and replace it) if it is:

  • Saturated, leaking, or no longer containing fluid
  • Torn, delaminated, or missing its backing integrity
  • Contaminated beyond the intended use area
  • Causing patient discomfort due to bunching, ridges, or heat buildup

If a recurring pattern is observed (for example, repeated leakage with a specific lot), treat it as a quality signal rather than a one-off.

When to escalate to biomedical engineering or the manufacturer

Underpad chux are consumables, so escalation is usually to materials management, infection prevention, and procurement. However, biomedical engineering may be involved when:

  • There is an institutional product evaluation that impacts patient safety workflows across devices (beds, support surfaces, monitoring cables, accessories).
  • Compatibility concerns arise with hospital equipment (for example, mattress systems, specialty beds, imaging table protocols).

Escalate to the manufacturer (or brand owner) when:

  • There is suspected product defect, unexpected failure, or unusual material shedding.
  • A lot/traceability issue is identified.
  • Facility policy requires reporting and follow-up for complaints or adverse events.

In all cases, document the product identifier information available (lot/batch, SKU, size, absorbency, and date of use) according to your quality management process.

In addition, many facilities escalate internally when:

  • Product performance affects throughput (bed closures due to mattress contamination, delays in admissions).
  • Waste volumes spike unexpectedly (which can indicate misuse, over-layering, or a mismatch between pad selection and patient need).
  • Staff injuries occur linked to improper pad use during repositioning (a training and manual-handling issue rather than a product defect in many cases).

Infection control and cleaning of Underpad chux

Cleaning principles (and where cleaning actually applies)

Most Underpad chux are single-use and are disposed of after contamination; they are not “cleaned.” Infection control focuses on:

  • Safe removal and containment
  • Correct waste segregation
  • Environmental cleaning of the surfaces that were protected (or exposed)

Reusable underpads do exist (varies by manufacturer and local purchasing), and these require laundering and inspection rather than routine disinfection at bedside.

For reusable programs, facilities typically define:

  • how soiled reusable pads are bagged at point of use,
  • whether they are treated as contaminated linen,
  • minimum laundering parameters (temperature, chemistry, and drying),
  • inspection criteria for membrane damage or edge fraying, and
  • a retirement/lifecycle plan to prevent degraded pads from re-entering circulation.

Disinfection vs. sterilization (general)

  • Sterilization: Typically reserved for devices labeled as sterile and intended to be used in sterile fields. Most Underpad chux are not sterile unless explicitly labeled.
  • Disinfection: Applies to the bed, mattress cover, chair, or table surface after pad removal if contamination is suspected or confirmed, following facility-approved disinfectants and contact times.

Always follow your facility’s environmental cleaning and infection prevention protocols, which may be more stringent than general guidance.

High-touch points to remember

Underpad chux protect surfaces, but staff often touch surrounding areas during changes. Commonly missed high-touch points include:

  • Bed rails, bed controls, and nurse call buttons
  • Mattress seams and zipper areas on mattress covers
  • Wheelchair armrests and brake levers
  • Stretcher side rails and handles
  • Overbed tables and bedside lockers
  • Commode chair surfaces and splash-prone areas

In high-turnover areas (ED, imaging, transport), it can also be helpful to remember:

  • stretcher push bars and steering handles,
  • IV pole adjustment points,
  • monitor leads or cable routing points that may rest on bedding, and
  • privacy curtains (depending on local cleaning responsibilities and schedules).

Example cleaning workflow (non-brand-specific)

  1. Perform hand hygiene and don appropriate PPE.
  2. Roll the soiled Underpad chux inward (contaminated side in) to reduce aerosolization and dripping.
  3. Dispose according to local waste policy (general waste vs regulated medical waste depends on jurisdiction and contamination type).
  4. If any fluid reached the underlying surface, clean visible soil first, then disinfect using facility-approved products and required contact time.
  5. Allow surfaces to dry fully before placing new linens or a new pad.
  6. Perform hand hygiene after glove removal and after touching cleaned surfaces.

Storage and handling to reduce contamination risk

  • Store Underpad chux in clean, dry areas off the floor.
  • Keep cartons closed when not actively restocking.
  • Avoid bringing bulk cartons into isolation rooms unless policy allows; use a cleanable caddy or pull only required quantity.
  • Rotate stock (first-expire/first-out where expiry exists; not publicly stated for all products).

Because underpads are often stored in large cartons, facilities in humid climates or older buildings sometimes add simple controls such as:

  • keeping cartons away from sinks, showers, and external walls prone to condensation,
  • using covered shelving to reduce dust exposure, and
  • avoiding over-stacking that crushes pads and can deform the absorbent core.

Medical Device Companies & OEMs

Manufacturer vs. OEM (Original Equipment Manufacturer)

In the Underpad chux market, the name on the box may not always be the entity that physically manufactures the product.

  • Manufacturer (brand owner / legal manufacturer): The organization responsible for product specifications, labeling, regulatory declarations (where applicable), complaint handling, and recalls.
  • OEM: The entity that produces the item (or major components) under contract for one or multiple brands, sometimes across multiple regions.

In practice, an OEM relationship can be perfectly acceptable—often essential for scale—but it changes how buyers should assess risk.

How OEM relationships impact quality, support, and service

For procurement and biomedical/quality teams, OEM dynamics can affect:

  • Consistency: Changes in OEM, materials, or production lines can change absorbency and leakage performance without obvious packaging differences.
  • Traceability: Clear lot/batch labeling and complaint pathways are critical when multiple OEM sources exist.
  • Quality systems: Certifications and audits (for example, ISO-based quality systems) vary by manufacturer and region; verify during vendor qualification.
  • Support and responsiveness: The brand owner’s complaint handling process matters more than the OEM’s identity for end users, but both influence resolution speed.
  • Regulatory compliance: Whether Underpad chux are regulated as a medical device or consumer hygiene product varies by country; responsibilities follow local law.

A practical procurement implication is change control: even when the box looks identical, the supplier may change core materials, backing film thickness, or adhesive chemistry. Contracts and vendor agreements sometimes include clauses requiring notification of material/OEM changes, which can help prevent “silent” performance drift.

Practical product evaluation criteria (non-clinical)

When facilities run in-use trials or compare bids, the following criteria are commonly assessed in addition to unit price:

  • Absorption speed (acquisition): Does fluid disappear quickly from the top surface?
  • Rewet/rewick: After absorption, does the top sheet feel dry, or does moisture return with pressure/movement?
  • Edge leakage resistance: How often do leaks occur at the sides or corners during typical patient movement?
  • Pad stability: Does it migrate on common mattress covers or chair materials?
  • Tensile strength: Does it tear during normal handling (without being used as a transfer aid)?
  • Noise and comfort: Patient-reported comfort and perceived quality.
  • Carton durability and storage footprint: Does packaging protect the product during transport and storage?

These are operational questions that frontline staff can answer quickly during a short pilot, often yielding more useful insight than relying on absorbency labels alone.

Top 5 World Best Medical Device Companies / Manufacturers

The following are example industry leaders often associated with healthcare consumables and/or absorbent hygiene products. This is not a verified ranking, and availability of Underpad chux varies by manufacturer and country.

  1. Essity – Essity is a well-known global hygiene and health company with established incontinence care portfolios in many regions. It is commonly associated with absorbent product categories used in institutional and home-care settings. Product naming, absorbency ranges, and distribution models vary by country and channel.

  2. Paul Hartmann AG (HARTMANN) – HARTMANN is widely recognized in medical consumables, wound care, and incontinence management across multiple markets. The company is commonly present in hospital procurement catalogs, especially in Europe and parts of Asia-Pacific. Specific underpad constructions and formulary positioning differ by region.

  3. Ontex – Ontex is an international personal hygiene group often linked to private-label and branded absorbent hygiene products. In some markets, Ontex-associated portfolios include institutional incontinence items that overlap with Underpad chux use cases. OEM/private-label relationships are common in this segment, so brand-owner clarity is important during purchasing.

  4. ABENA – ABENA is commonly referenced in healthcare and hygiene consumables, including continence care products used in long-term care and hospitals. Many buyers value predictable SKU structures and institutional packaging formats, though local availability and tender participation vary. Product claims and features should be verified against the local IFU.

  5. Medline Industries – Medline is a major provider of healthcare supplies and often offers private-label consumables across acute and post-acute care. In many systems, Medline functions as both a brand owner and a supply-chain partner, which can simplify standardization and contract management. The extent of global footprint and local manufacturing depends on region and is not publicly stated in a uniform way.

Vendors, Suppliers, and Distributors

Role differences: vendor vs. supplier vs. distributor

In day-to-day purchasing conversations these terms are often used interchangeably, but they can mean different things operationally:

  • Vendor: A general term for the party selling the product to your facility (could be a manufacturer, distributor, or marketplace seller).
  • Supplier: Often used to describe a contracted source responsible for meeting defined service levels (fill rate, lead time, substitutions, returns).
  • Distributor: A company focused on warehousing, logistics, order fulfillment, and sometimes value-added services (kit assembly, EDI integration, inventory management).

For Underpad chux, distributors play an outsized role because the products are bulky, high-throughput, and sensitive to storage conditions (crushing, moisture, carton damage).

For supply chain teams, underpads behave differently from many small consumables:

  • Cube matters: The storage footprint can be larger than the value of the inventory, making par-level planning important.
  • Substitution is common during shortages: Because many products look similar, substitution risk needs clear governance so clinical areas don’t receive unsuitable alternatives.
  • Last-mile handling affects quality: Cartons stored on floors, near doors, or in damp areas can lead to crushed cores or compromised packaging.

Top 5 World Best Vendors / Suppliers / Distributors

The following are example global distributors in healthcare supply chains (not a verified ranking). Regional reach and Underpad chux portfolio availability vary.

  1. McKesson – McKesson is widely known for large-scale healthcare distribution, particularly in North America. For institutional buyers, strengths often include standardized ordering, contract management, and broad med-surg catalogs. International availability and specific incontinence lines vary by market.

  2. Owens & Minor – Owens & Minor operates healthcare logistics and distribution services that can include med-surg consumables. Many health systems engage such distributors for integrated supply programs, inventory services, and PPE/consumables management. Product selection and private-label availability differ by country.

  3. Henry Schein – Henry Schein is recognized for healthcare distribution, historically strong in dental and ambulatory settings, with medical supply offerings in many regions. Buyers may encounter Henry Schein in clinic networks, outpatient surgery, and office-based care procurement. Hospital-scale distribution and underpad selection depend on local operations.

  4. DKSH – DKSH is known for market expansion and distribution services in parts of Asia and beyond, supporting multinational and regional healthcare brands. Where present, it may provide regulatory, marketing, warehousing, and last-mile support alongside distribution. Portfolio breadth for Underpad chux depends on the specific country operation.

  5. Bunzl – Bunzl is a distribution and outsourcing group with healthcare-related distribution businesses in several regions. Its strengths often center on logistics for disposable products and contract supply to institutions. Specific medical catalogs and local regulatory support vary by subsidiary and geography.

In distributor-managed environments, it is common to formalize additional expectations such as:

  • acceptable substitution rules (what can replace what, and who signs off),
  • carton quality requirements (no crushed cases delivered to wards),
  • delivery frequency and emergency replenishment for bulky items, and
  • procedures for returns or credit when packaging is water-damaged or contaminated in transit.

Global Market Snapshot by Country

India

Demand for Underpad chux in India is driven by expanding private hospitals, growing long-term care needs, and higher expectations for patient dignity and infection prevention in urban facilities. Procurement is often price-sensitive, with a mix of domestic manufacturing and imported brands depending on quality tier. Rural access can be constrained by distribution reach and storage conditions for bulky consumables.

In addition, hot and humid conditions in some regions can make storage and carton integrity more challenging, increasing the importance of dry warehousing and stock rotation. Large hospital groups may standardize SKUs across networks, while smaller facilities may buy opportunistically based on availability.

China

China’s market is influenced by large hospital networks, rapid modernization in top-tier cities, and expanding elder care needs. Domestic manufacturing capacity is significant, and private-label/OEM models are common, while premium institutional products may still rely on imports in some channels. Urban facilities typically have stronger supply-chain infrastructure than county-level hospitals.

Quality variability can be a key procurement issue: buyers often focus on consistent absorbency performance across lots, and large systems may require stronger documentation on specifications, labeling, and traceability.

United States

In the United States, Underpad chux are high-volume consumables across acute care, post-acute, and home health, with procurement strongly shaped by GPO contracts and standardized SKUs. Demand is tied to staffing efficiency, pressure injury programs, and infection prevention workflows, alongside reimbursement and documentation requirements in post-acute settings. Domestic and imported sourcing both exist, with strong distributor influence on availability.

Waste handling and cost accounting can also influence product choice, as some facilities weigh solid-waste costs against laundry capacity and linen replacement rates. Substitution management during backorders is a recurring operational concern.

Indonesia

Indonesia’s demand is concentrated in urban hospitals and private networks, with ongoing expansion in healthcare capacity and a growing focus on patient experience. Many facilities rely on distributors for consistent supply, and import dependence can be higher for premium or specialized variants. Logistics across islands can affect lead times, warehousing, and carton integrity.

Facilities often plan higher buffer stock for bulky items like underpads due to delivery variability, particularly outside major metropolitan areas.

Pakistan

Pakistan’s market is shaped by a mix of public hospitals and a sizeable private sector in major cities, where consumable standardization is increasing. Price sensitivity remains a major driver, with variable access to higher-absorbency products outside urban centers. Import reliance can be significant for certain brands, and procurement processes may differ widely between provinces and institutions.

In some settings, underpads may be reserved for higher-acuity areas due to budget constraints, which increases the value of targeted use protocols and staff training on correct placement.

Nigeria

In Nigeria, demand is growing in tertiary hospitals and private facilities, particularly in major urban areas where infection prevention expectations are rising. Supply can be constrained by import dependence, currency fluctuations, and distribution challenges, which drives interest in reliable local partners and buffer stock planning. Rural and smaller facilities may face limited product choice and inconsistent availability.

Power and storage infrastructure can also influence product condition; facilities with limited climate control may prioritize packaging durability and moisture resistance.

Brazil

Brazil has a large, diverse healthcare system with demand spanning public networks and private hospital groups, and procurement is often influenced by tenders and contract frameworks. Domestic production exists for many hygiene consumables, while certain premium institutional products may be imported. Service ecosystems are stronger in major metropolitan areas than in remote regions.

Hospitals may balance underpad use against laundry capacity and local waste management rules, and product standardization can vary between states and hospital networks.

Bangladesh

Bangladesh’s demand is concentrated in urban hospitals, maternity services, and rapidly growing private clinics, where surface protection and workflow efficiency are increasingly prioritized. Price and availability drive purchasing decisions, and facilities may use multiple brands depending on supply continuity. Import dependence and distribution capacity can affect consistency outside Dhaka and other major cities.

Because storage space can be limited in crowded facilities, carton size, case-pack configuration, and predictable delivery schedules can be as important as absorbency labels.

Russia

Russia’s market reflects large regional hospital systems and public procurement processes that can emphasize standardization and domestic sourcing preferences. Availability of imported Underpad chux may vary by region due to logistics and regulatory pathways, while local manufacturing and private-label options can fill gaps. Service and distribution tend to be stronger in major cities than in remote areas.

Facilities may prioritize documentation and specification compliance during tenders, and regional differences can influence which brands are consistently available.

Mexico

Mexico’s demand comes from public institutions and expanding private hospital networks, with strong distributor influence on product availability and contract compliance. Import and domestic sourcing both play roles, and hospitals often balance absorbency performance against cost and waste handling constraints. Urban centers typically have wider brand choice than rural facilities.

In some networks, underpads are bundled into broader med-surg contracts, so product changes may occur during contract renewals and require coordinated staff communication.

Ethiopia

In Ethiopia, Underpad chux use is most common in larger urban hospitals and private facilities where supply chains can support consistent consumable availability. Import dependence is often significant, and procurement can be affected by lead times and constrained budgets. Building reliable distribution and storage practices is central to improving access beyond major cities.

Facilities may prioritize multipurpose, cost-effective pads that can serve both beds and chairs, while still needing clear guidance to avoid misuse as transfer aids.

Japan

Japan’s demand is supported by an aging population, high expectations for continence care quality, and mature hospital and long-term care infrastructure. Domestic manufacturers and established distributors play a major role, and product specifications may be closely aligned with comfort and skin-friendly performance. Standardization and consistent supply are typically strong, though product requirements can be exacting.

There is often a strong emphasis on patient comfort, quiet materials, and predictable performance, particularly in long-term care environments where underpads may be used frequently.

Philippines

The Philippines shows growing demand in urban hospitals, BPO-linked private healthcare, and long-term care needs, with consumables procurement often managed through distributors and import channels. Logistics across islands can influence availability, pricing, and carton condition, making forecasting and buffer stock important. Rural facilities may have limited access to higher-tier product variants.

Facilities sometimes standardize to fewer SKUs to reduce confusion and ensure consistent stocking across multiple island-based sites.

Egypt

Egypt’s market is driven by large public hospitals and a sizable private sector, with increasing attention to infection prevention and patient experience in higher-acuity facilities. Import dependence can be higher for premium products, while local production and regional supply chains may cover baseline needs. Distribution strength and purchasing power differ between Cairo/Alexandria and more remote governorates.

Tender processes and public procurement rules can influence product choice, and some facilities may prioritize local availability and continuity over premium features.

Democratic Republic of the Congo

In the DRC, demand is concentrated in major cities and in facilities supported by private investment or international programs, where basic surface protection and fluid containment supplies are prioritized. Import reliance and challenging logistics can limit product variety and continuity, making local distributor capability a key differentiator. Rural access is often constrained by transport, storage, and budget realities.

In such contexts, training on targeted use and rapid disposal can improve both cost control and infection prevention outcomes when supplies are limited.

Vietnam

Vietnam’s demand is growing with hospital modernization, expanding private healthcare, and rising expectations for patient comfort and cleanliness. Distribution networks in major cities support broader brand availability, while provincial facilities may rely on fewer suppliers and more price-driven selection. Import and domestic production coexist, and OEM/private-label models are common in consumables.

Hospitals often evaluate underpads in relation to housekeeping performance metrics and bed turnover speed, especially in higher-volume urban facilities.

Iran

Iran’s market reflects a combination of domestic manufacturing and import pathways that may vary over time due to regulatory and trade conditions. Large urban hospitals typically have more stable access to institutional-grade consumables through established procurement systems. Outside major cities, availability and product selection can be more variable, emphasizing the need for standardized, resilient supply planning.

Facilities may maintain higher safety stock for high-throughput items and prefer suppliers who can provide consistent specifications over time.

Turkey

Turkey has a strong healthcare delivery system with both public and private procurement, and a developed manufacturing base for many medical consumables. Demand for Underpad chux is supported by hospital throughput and long-term care needs, with competitive local brands alongside imported options. Distribution and service ecosystems are generally stronger in western urban regions than in more remote areas.

Private hospital groups may run formal product evaluations focused on patient comfort and leakage rates, while public systems may emphasize standardized tender specifications.

Germany

Germany’s demand is shaped by mature hospital infrastructure, strong long-term care services, and structured procurement processes with emphasis on compliance and quality documentation. Domestic and EU-based manufacturing plays a major role, and product specifications often focus on predictable performance and skin-friendlier designs. Distribution is highly organized, supporting consistent availability across regions.

Facilities may also weigh sustainability initiatives, including waste reduction and evaluated use of reusable alternatives where laundry systems can support them.

Thailand

Thailand’s market is supported by major urban hospitals, private healthcare networks, and medical tourism in some areas, where patient experience and housekeeping standards are closely monitored. Import and domestic sourcing both contribute, with distributors often managing brand access and contract supply. Rural access can vary, and hospitals may standardize to a limited number of SKUs to ensure continuity.

In tourist-facing or premium private facilities, comfort and perceived quality (softness, noise, dryness) may receive greater emphasis alongside absorbency.

Key Takeaways and Practical Checklist for Underpad chux

  • Standardize Underpad chux SKUs by ward to reduce selection errors and waste.
  • Treat Underpad chux as hospital equipment that affects safety, cost, and throughput.
  • Select size first, then absorbency, based on expected fluid exposure and patient movement.
  • Confirm absorbent side up and backing side down every time during placement.
  • Avoid wrinkles and bunching to reduce friction and discomfort under the patient.
  • Do not use Underpad chux as a lifting, dragging, or transfer aid.
  • Keep Underpad chux off the floor to prevent slip hazards and contamination.
  • Replace Underpad chux promptly when wet or soiled per facility protocols.
  • Use wings/tucks or non-slip options where migration and bunching are recurring problems.
  • Do not assume “heavy” absorbency is standardized across manufacturers.
  • Verify packaging integrity and quarantine damaged cartons according to policy.
  • Capture lot/batch details when required for traceability and complaint handling.
  • Integrate Underpad chux use into skin integrity workflows and moisture management routines.
  • Avoid excessive layering that can trap heat and moisture and reduce mattress performance.
  • Coordinate with wound care and continence teams on placement practices for high-risk patients.
  • Use appropriate PPE and standard precautions during removal and disposal.
  • Roll the soiled pad inward to contain contaminants and reduce dripping during disposal.
  • Dispose of Underpad chux according to local waste segregation rules and contracts.
  • Clean and disinfect any exposed surfaces using approved products and contact times.
  • Pay attention to bed rails, controls, and call buttons during changes as high-touch points.
  • Train staff that Underpad chux do not provide measured fluid output data.
  • Use observational cues (leakage, strike-through, saturation) as operational quality signals.
  • Escalate repeated failures by SKU or lot to procurement and the manufacturer for investigation.
  • Include Underpad chux in new staff competency checklists for basic care workflows.
  • Ensure storage areas are dry, clean, and organized to prevent carton crushing and moisture damage.
  • Plan buffer stock for bulky Underpad chux, especially in facilities with constrained deliveries.
  • Align Underpad chux selection with mattress cover materials and bed features to reduce sliding.
  • Avoid adhesives on skin and verify adhesive compatibility with facility surfaces.
  • Confirm whether a product is sterile only if it is explicitly labeled as sterile.
  • Use procedure-specific drapes when a sterile field is required instead of standard Underpad chux.
  • Involve infection prevention teams when changing products that affect containment and cleaning workload.
  • Track pad consumption trends to identify overuse, misuse, or workflow inefficiencies.
  • Evaluate products with simple in-use trials focused on leakage rates and staff handling feedback.
  • Consider total cost of ownership, including laundry, EVS labor, waste disposal, and mattress protection.
  • Define clear responsibilities for routine checks so pads are not left saturated for long periods.
  • Use consistent naming (“Underpad chux”) in internal catalogs to reduce ordering confusion.
  • Ensure transport teams stock Underpad chux for stretchers where contamination risk is predictable.
  • Review country-specific regulatory and labeling expectations before importing or switching suppliers.
  • Maintain a documented complaint pathway so frontline staff can report failures without friction.
  • Treat recurring skin irritation reports as a trigger for product review, not just a care issue.
  • Coordinate with biomedical engineering when product changes affect bed systems or specialty surfaces.
  • Require suppliers to disclose OEM changes or material changes where contracts allow.
  • Avoid substituting similar-looking products without clinical and operational sign-off.
  • Keep Underpad chux accessible at point of care to reduce delays and rushed placement errors.

Additional practical reminders that often improve consistency:

  • Run brief refresher training after any brand/SKU change so staff recognize differences in look and feel.
  • If reusable underpads are used, define clear linen bagging and laundry workflows to prevent cross-contamination.
  • For chair use, confirm the pad does not overhang to the floor where it can pick up contaminants.
  • Treat repeated leakage events as a system problem (placement, size, bed angle, substitution) before blaming staff.

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