Clinical question

Should supplementation with collagen versus no supplementation/standard supplements be used to promote healing in adults with PIs?

Context

Population:

Intervention:

Comparison:

Main Outcomes:

Setting:

Conflicts on Interest:

Adults who have a pressure injury

Collagen supplement

Standard diet or standard supplement or placebo

Any clinical setting

Hierarchy of outcome measures:

  • Outcome 1: Time to healing

  • Outcome 2:  Complete healing (total/percent healed)

  • Outcome 3: Change in wound size (% change)

  • Outcome 4: Pain

  • Outcome 5: If infected at baseline, changes in signs and symptoms of infection

No Guideline Governance Group members of Core Review Group members had a conflict of interest

Evidence to Decision Framework

(Click on the individual judgements for more information)

Summary of Judgements

1.

2.

3.

4.

5.

6.

7.

8.

9.

10.

11.

12.

Yes

Small

Large

Moderate

No important uncertainty or variability

Does not favor either the intervention or the comparison

Moderate costs

No included studies

No included studies

Probably increased

Varies

Varies

1. Problem:
Is the problem (pressure injuries) a priority?

JUDGEMENT

  • No

  • Probably No

  • Probably Yes

  • Yes

  • Varies

  • Don’t Know

RESEARCH EVIDENCE

Treating pressure injuries to achieve healing is a priority to most individuals who experience a PI. In 2021, the Guideline Governance Group undertook a stakeholder survey on priority issues to address in the guideline. Receiving clinical guidance on nutritional interventions for treating pressure injuries (PIs) was rated as the highest priority by clinicians (median ranking 5/5) and people with or at risk of PIs and their informal carers (median ranking 5/5).  Clinical guidance on nutritional interventions for treating PIs was rated as a high priority by researchers (median ranking 4/5) and industry representatives (median ranking 4/5).

In an earlier survey conducted by the previous Guideline Governance Group in 2018,(Haesler, Pittman et al. 2022) 71.8% (275/383) of individuals with or at risk of PIs and 65.3% (555/850) of informal carers rated receiving information on diet and hydration as important or very important. 

2. Desirable Effects:
How substantial are the desirable anticipated effects?

JUDGEMENT

  • Trivial

  • Small

  • Moderate

  • Large

  • Varies

  • Don’t Know

RESEARCH EVIDENCE

>
Outcome Collagen
supplement
No
supplement
Difference Relative effect
Change in PI surface area (cm2) -- Mean change 5cm2
Mean difference 1.8cm2 lower(from 3.36 lower to 0.26lower) --

Outcome 1: Change in PI surface area (cm2)

The forest plot (Langer, Wan et al. 2024) included one RCT (Sugihara, Inoue et al. 2018) providing evidence on the effectiveness of high dipeptide collagen supplementation for improving PI surface area versus a placebo supplement.** The supplements were taken for 16 weeks by individuals  with Category/Stage 2 or 3 PIs. Individuals who were malnourished, or who had diabetes, arterial or venous disease, smokers or any other condition that might impact wound healing were not eligible for inclusion in the study. The analysis showed that collagen supplementation might be associated with better healing, demonstrated by a mean difference in wound area (cm2) of 1.8cm2 lower (from 3.36cm2 lower to 0.26cm2 lower). There was moderate certainty in this result. The certainty was downgraded once for imprecision because there was a low number of events and participants (Langer, Wan et al. 2024).

** Regimens are described in the data extraction tables. Product names may have changed.

3. Undesirable Effects:
How substantial are the undesirable anticipated effects?

JUDGEMENT

  • Trivial

  • Small

  • Moderate

  • Large

  • Varies

  • Don’t Know

Outcome Collagen
supplement
No
supplement
or placebo
Difference Relative effect
Adverse GIT events 5/96 (5.2%) 1/58 (1.72%) 46 more per 1000
(from 6 more to 384 more)
RR 2.69
(0.33 to 22.30)

Outcome: Adverse GI events

The meta-analysis (Langer, Wan et al. 2024) included two RCTs (Yamanaka, Okada et al. 2017, Sugihara, Inoue et al. 2018) that reported adverse gastrointestinal tract (GIT) effects associated with low and high dipeptide collagen supplements. Compared to not taking a supplement, there was a non-significant higher rate of GIT events associated with the intervention (5.2% vs 1.72%, RR 2.69, 95% CI 0.33 to 22.30, p=0.36). This translated to 46 more individuals per 1,000 experiencing an adverse GIT event (from 6 more to 384 more). Reported adverse events included moderate constipation and moderate diarrhea. However, there is very low certainty in this result. The certainty was downgraded once for some concerns regarding the overall risk of bias for one included study (Langer, Wan et al. 2024). The certainty was also downgraded twice for imprecision because the confidence interval (CI) overlaps the null effect and includes potential benefit (RR<0.75) and potential harm (RR>1.25), and because there was a low number of events and participants (Langer, Wan et al. 2024).

4. Overall certainty of evidence: What is the overall certainty of the evidence of effects?

JUDGEMENT

  • Very low

  • Low

  • Moderate

  • High

  • No included studies

RESEARCH EVIDENCE

Outcome Relative Importance Certainty of Evidence
Change in PI surface area (cm2) CRITICAL MODERATE

There is no core outcome set specific to pressure injury healing. To determine the relative importance of outcome measures, the GGG reviewed literature (Gottrup, Apelqvist et al. 2010, Augustin, Schmitt et al. 2014, Driver, Gould et al. 2017, Driver, Gould et al. 2019, Miranda, Deonizio et al. 2021, Raepsaet, Alves et al. 2023, Gupta, Goldstone et al. 2024, Zhang, Zhang et al. 2024), on PI and wound healing outcome measures and, in 2021, undertook a survey of stakeholders regarding their perspective on the importance of commonly reported wound healing outcomes. Based on the review and survey, the GGG prioritized consideration of the following five outcome measures of interest when evaluating evidence for interventions to support PI healing. These clinical outcomes were supported by all surveyed stakeholder groups as critically important to making decisions about the evidence, and are wound agnostic (Gupta, Goldstone et al. 2024), frequently reported in PI research (Miranda, Deonizio et al. 2021), and relevant to both clinical practice and quality of life for individuals with a PI (Driver, Gould et al. 2017, Driver, Gould et al. 2019).

Priority for outcome measures was:

  • Time taken to heal

  • Complete healing

  • Percent change in wound size

  • Wound-related pain

  • Changes in signs and symptoms of infection (if infected at baseline)

Certainty of evidence for outcome measures

Certainty of evidence for change in PI area (in cm2) was downgraded once for imprecision because there was a low number of events and participants (Langer, Wan et al. 2024).

5. Values:
Is there important uncertainty about or variability in how much people value the main outcomes?

JUDGEMENT

  • Important uncertainty or variability

  • Possibly important uncertainty or variability

  • Probably no important uncertainty or variability

  • No important uncertainty or variability

RESEARCH EVIDENCE

In a Delphi survey (Lechner, Coleman et al. 2022) that developed a core outcomes et for PI prevention trials, the outcome of PI occurrence was rated as being of critical important (score of 7-9) by all types of stakeholders (health professionals, people with or at risk of a PI and their informal carers, industry representatives and researchers). Greater than 90% of the 158 participants rated this outcome measure as critically important (Lechner, Coleman et al. 2022).

6. Balance of Effects:
Does the balance between desirable and undesirable effects favour the intervention or the comparison?

JUDGEMENT

  • Favors the comparison

  • Probably favors the comparison

  • Does not favor either the intervention or the comparison

  • Probably favors the intervention

  • Favors the intervention

  • Varies

  • Don’t know

RESEARCH EVIDENCE

The desirable effects were small, with a large confidence interval and individuals with poorer healing were excluded from the studies. The undesirable effects were considered large. The Guideline Governance Group considered that the balance of effects favored neither the intervention nor comparison.

7. Resources Required:
How large are resource requirements (costs) of the intervention?

JUDGEMENT

  • Large costs

  • Moderate costs

  • Negligible costs and savings

  • Moderate savings

  • Large savings

  • Varies

  • Don’t know

RESEARCH EVIDENCE

In the Panel Group’s expert opinion, nutritional supplementation can be expensive, particularly for homeless people, people living in the community, people in long term institutional settings, and those without access to health insurance. This is a particular concern for people who require supplementation for longer duration. In acute care settings, particularly intensive care, nutritional supplements are usually funded within the costs of health care.

In the Guideline Governance Group’s expert opinion, the above costs represent moderate costs of implementing the nutritional supplementation.

8. Certainty of evidence of required resources:
What is the certainty of evidence of resource requirements (costs) of the intervention?

JUDGEMENT

  • Very low

  • Low

  • Moderate

  • High

  • No included studies

RESEARCH EVIDENCE

No included studies

9. Cost Effectiveness: Does the cost-effectiveness of the intervention favour the intervention or the comparison?

JUDGEMENT

  • Favors the comparison

  • Probably favors the comparison

  • Does not favor either the intervention or the comparison

  • Probably favors the intervention

  • Varies

  • No included studies

RESEARCH EVIDENCE

No included studies

10. Inequity:
What would be the impact of recommending the intervention on health inequity?

JUDGEMENT

  • Reduced

  • Probably reduced

  • Probably no impact

  • Probably increased

  • Increased

  • Varies

  • Don’t know

RESEARCH EVIDENCE

In the Panel Group’s expert opinion, people who are at higher risk of nutritional deficits are also more likely to be unable to access nutritional supplementation due to their social circumstances and the cost of interventions. This includes barriers to accessing a dietitian to evaluate the person’s nutritional needs. In the Guideline Governance Group’s expert opinion, recommending nutritional supplementation would likely increase health inequity. There are barriers to accessing supplementation for many people depending on their geographic location and the clinical context.

11. Acceptability:
Is the intervention acceptable to key stakeholders?

JUDGEMENT

  • No

  • Probably no

  • Probably yes

  • yes

  • Varies

  • Don’t know

RESEARCH EVIDENCE

There is some evidence that arginine/micronutrient supplements are acceptable. In one study (Banks, Ross et al. 2016), there was a nonsignificant higher rate of non-adherence to supplementation compared with standard diet (29.67% versus 0%, RR 15.60, 95% CI 0.94 to 259, p=0.06, very low certainty of evidence) (Langer, Wan et al. 2024).

In the Panel Group’s expert opinion, a wide range of factors influence acceptability of nutritional supplements. These include palatability of thickened supplements and altered foods (e.g. pureed or thickened) and the person’s ability to consume the volume of fluid required for some supplements

In the Guideline Governance Group’s expert opinion, recommending nutritional supplementation would having varying acceptability from stakeholders.

12. Feasibility:
Is the intervention (limiting sitting time) feasible to implement?

JUDGEMENT

  • No

  • Probably no

  • Probably yes

  • yes

  • Varies

  • Don’t know

RESEARCH EVIDENCE

In the Panel Group’s expert opinion, barriers to implementation include access to a dietitian to ensure the intervention can be individualized to the person’s needs. Nutritional supplementation is not available in many clinical and geographic contexts, and in some contexts there are rigid referral mechanisms to access dietitians and nutritional interventions.

In the Panel Group’s expert opinion, people living in the community may be unable to implement the recommendation due to lack of relevant knowledge to select an appropriate supplement.

In the Guideline Governance Group’s expert opinion, the feasibility of implementing a recommendation to provide nutritional supplementation varies. In some contexts (e.g. most acute care settings) access to nutritional supplementation and the processes that support implementation (e.g. screening for nutritional deficits, dietician review, access to products) is highly feasible. In other contexts (e.g., community settings, low resource communities) implementing a recommendation to provide nutritional supplementation would not be feasible.

References

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Driver, V. R., L. J. Gould, P. Dotson, L. L. Allen, M. J. Carter and L. L. Bolton (2019). "Evidence supporting wound care end points relevant to clinical practice and patients' lives. Part 2. Literature survey." Wound Repair Regen 27(1): 80-89.

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Gottrup, F., J. Apelqvist and P. Price (2010). "Outcomes in controlled and comparative studies on non-healing wounds: recommendations to improve the quality of evidence in wound management." J Wound Care 19(6): 237-268.

Gupta, R., L. Goldstone, S. Eisen, D. Ramachandram, A. Cassata, R. D. J. Fraser, J. L. Ramirez-GarciaLuna, R. Bartlett and J. Allport (2024). "Towards an AI-based objective prognostic model for quantifying wound healing." IEEE J Biomed Health Inform 28(2): 666-677.

Haesler, E., J. Pittman, J. Cuddigan, S. Law, Y. Y. Chang, K. Balzer, D. Berlowitz, K. Carville, J. Kottner, M. Litchford, Z. Moore, P. Mitchell and D. Sigaudo-Roussel (2022). "An exploration of the perspectives of individuals and their caregivers on pressure ulcer/injury prevention and management to inform the development of a clinical guideline." J Tissue Viability 31(1): 1-10.

Langer, G., C. S. Wan, A. Fink, L. Schwingshackl and D. Schoberer (2024). "Nutritional interventions for preventing and treating pressure ulcers." Cochrane Database Syst Rev 2: CD003216.

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