Compromised Grafts and Flaps and HBOT | Canada Hyperbarics
UHMS Indication #12 Level B - Moderate Evidence

Compromised Grafts and Flaps and HBOT

Hyperbaric oxygen therapy improves the survival of skin grafts and surgical flaps at risk of failure by enhancing tissue oxygenation at the graft-wound interface during the critical period before durable neovascularisation establishes a permanent blood supply. It is used both to prepare compromised recipient sites before grafting (most commonly irradiated tissue) and to rescue grafts and flaps that show early signs of failure after surgery. Compromised grafts and flaps is recognised by Health Canada as one of the 14 conditions for which provincial health insurance covers HBOT at hospital-based programmes.

· Canada Hyperbarics Editorial Team · Sources

Quick Answer

Does HBOT help compromised grafts and flaps? Hyperbaric oxygen therapy improves the survival of skin grafts and surgical flaps at risk of failure by enhancing tissue oxygenation at the graft-wound interface during the critical period before durable neovascularisation establishes a permanent blood supply. It is used both to prepare compromised recipient sites before grafting (most commonly irradiated tissue) and to rescue grafts and flaps that show early signs of failure after surgery. Compromised grafts and flaps is recognised by Health Canada as one of the 14 conditions for which provincial health insurance covers HBOT at hospital-based programmes.

What Is Compromised Grafts and Flaps?

Skin grafts and surgical flaps fail when the new blood supply at the recipient site is inadequate to support tissue survival during the early post-operative period. The critical biological window is the first 24 to 72 hours after surgery, before plasmatic imbibition and capillary inosculation give way to durable neovascularisation from the recipient bed. Graft and flap failure rates rise with anything that compromises the vascular bed: prior radiation, diabetes mellitus, peripheral vascular disease, active or recent smoking, prior surgical scarring, infection, malnutrition, advanced age, and the use of non-vascularised grafts in problematic anatomic locations.

The Health Canada-recognised hyperbaric indication encompasses several distinct surgical scenarios: split-thickness and full-thickness skin grafts in compromised wound beds, pedicled and free vascularised flaps showing early signs of compromise (pallor, cyanosis, congestion, or capillary refill changes), composite grafts (skin and underlying tissue, including ear and nose reconstructions), nipple-areola complex grafts after breast reconstruction, and replantation of avulsed segments. The clinical pattern that prompts HBOT consultation is typically a graft or flap that was placed with adequate surgical technique but is showing early signs of inadequate perfusion, often within hours to a day or two of the index operation.

HBOT can also be used pre-operatively in patients whose recipient site is known to be compromised (most commonly previously irradiated tissue) to support angiogenesis before the planned reconstruction. The Marx 20-and-10 protocol applied to head-and-neck reconstruction in irradiated jaws is the canonical example: 20 HBOT sessions before the planned graft and 10 sessions afterward.

How HBOT Helps

Hyperbaric oxygen therapy supports compromised grafts and flaps through three convergent mechanisms.

First, oxygen delivery during the critical pre-vascularisation window. Inside the chamber at 2.0 to 2.5 ATA on 100 percent oxygen, plasma oxygen content rises 10- to 15-fold, raising tissue pO2 in the graft-wound interface from ischemic levels to several hundred mmHg during each session. This intermittent hyperoxia keeps the graft and flap tissue alive long enough for plasmatic imbibition, capillary inosculation, and neovascularisation to establish a permanent blood supply.

Second, edema reduction at the graft-bed interface. Hyperoxic vasoconstriction reduces capillary permeability and tissue edema in well-oxygenated peri-graft tissue while preserving or improving oxygen delivery to the hypoxic graft itself. Reduced edema lowers diffusion distance and supports earlier vascular ingrowth.

Third, support for angiogenesis and fibroblast activity. The same VEGF-mediated angiogenesis that underpins HBOT's benefit in chronic wounds and radiation injury contributes to definitive vascularisation of the graft or flap recipient bed. Fibroblast proliferation and collagen cross-linking, both oxygen-dependent, support the structural integration of the graft into surrounding tissue. In pre-operative use for irradiated recipient sites, repeated HBOT sessions raise capillary density to approximately 75 to 80 percent of non-irradiated baseline before the planned surgery, substantially improving the probability of graft take.

Typical Treatment Protocol

Standard adjunctive protocol is 2.0 to 2.5 ATA on 100 percent oxygen for 90 minutes per session. Total course depends on the clinical scenario. For compromised post-operative grafts and flaps showing early signs of failure, treatment begins as soon as the diagnosis is recognised, typically within hours to a day or two of the index operation. Twice-daily sessions for the first 24 to 48 hours are followed by once-daily sessions for the remainder of the course. Total course is typically 10 to 20 sessions, guided by clinical response, capillary refill, colour, and (for flaps with monitoring) Doppler signal. For pre-operative preparation of compromised recipient sites (most commonly irradiated tissue), the Marx 20-and-10 protocol applies: 20 HBOT sessions before the planned graft or flap, 10 sessions afterward, total 30 sessions. The pre-operative phase stimulates angiogenesis in the recipient bed; the post-operative phase supports the graft during the critical pre-vascularisation window. HBOT is delivered as an adjunct to standard reconstructive-surgery management, never as a substitute for surgical re-exploration when revision is indicated. The decision to add HBOT, and whether to combine it with surgical revision, is made jointly by the plastic-surgery team and hyperbaric medicine.

Evidence Summary

B

Level B - Moderate Evidence

Supported by controlled studies and clinical evidence

Key Research Findings

Top studies in our database

Highest-evidence-tier studies tagged to this condition in the Canada Hyperbarics research database, ranked by evidence tier (1 = meta-analysis or RCT, 2 = cohort, 3 = case series), most recent first.

See all compromised grafts and flaps studies in our research database

What to Expect from Treatment

For post-operative compromised grafts and flaps, the plastic-surgery team typically recognises the early signs of failure (pallor, cyanosis, congestion, capillary refill changes) within hours to a day or two of the index operation and contacts the hospital hyperbaric programme directly. The decision to add HBOT, and whether to combine it with surgical re-exploration of the flap pedicle or graft bed, is made jointly. The first chamber session is typically delivered the same day as the consultation.

You change into cotton scrubs (no synthetic fabrics, no skin lotions, no jewellery), enter the chamber, and lie down (in a monoplace) or sit in a recliner (in a multiplace with multiple patients). Pressurisation takes five to ten minutes, the 90-minute treatment phase is on 100 percent oxygen at 2.0 to 2.5 ATA, and decompression takes another five to ten minutes. For critically ill patients, multiplace chambers accommodate ventilator-dependent and infusion-dependent support with a hyperbaric-trained nurse and physician inside the chamber.

Twice-daily sessions for the first 24 to 48 hours are followed by once-daily sessions through the remainder of the course. Total course is typically 10 to 20 sessions. The plastic-surgery team monitors the graft or flap clinically (colour, capillary refill, temperature, Doppler signal where applicable) at each visit. Pre-operative Marx 20-and-10 cases are scheduled around the planned reconstructive surgery date.

Accessing HBOT for Compromised Grafts and Flaps in Canada

Compromised grafts and flaps is recognised by Health Canada as one of the 14 conditions for which hyperbaric oxygen is the established adjunctive treatment. Coverage is provincial at the 11 hospital-based hyperbaric programmes across seven provinces.

In Ontario, OHIP covers treatment at the three hospital programmes (Toronto General / UHN, Hamilton General Hospital, The Ottawa Hospital). Toronto General has particularly close working relationships with the major reconstructive plastic-surgery teams in the GTA. Select eligible Independent Health Facilities may also bill OHIP for approved indications. In Alberta, Misericordia Edmonton (Covenant Health) and the Foothills Medical Centre / AJECCC Calgary (Alberta Health Services) accept compromised-graft referrals, with the Alberta hospital billing code 13.99I (per 15 minutes). British Columbia (MSP) covers treatment at Vancouver General Hospital. RAMQ covers treatment at Hôpital du Sacré-Cœur de Montréal and Hôtel-Dieu de Lévis in Quebec. MSI (Nova Scotia), MCP (Newfoundland and Labrador), and Saskatchewan also cover their respective hospital programmes.

For patients in provinces or territories without an in-province hospital programme (Manitoba, New Brunswick, Prince Edward Island, Yukon, Northwest Territories, Nunavut), inter-provincial referral is arranged through the receiving province's transfer service. The most common scenarios are post-operative graft compromise after reconstructive surgery in a referring province and pre-operative Marx-protocol preparation before planned reconstruction at a hospital with both plastic-surgery and hyperbaric capabilities.

Provincial Access for Compromised Grafts and Flaps

Hyperbaric oxygen therapy for the 14 Health Canada-recognised conditions, including Compromised Grafts and Flaps, is delivered at the 11 hospital hyperbaric programmes located in seven provinces (Ontario, Quebec, British Columbia, Alberta, Nova Scotia, Newfoundland and Labrador, and Saskatchewan). The six provinces and territories without an in-province hospital programme (Manitoba, New Brunswick, Prince Edward Island, Yukon, Northwest Territories, and Nunavut) route patients to the nearest receiving hospital programme. Use the links below for province-specific coverage, referral pathway, and emergency routing details.

For acute or emergency presentations of Compromised Grafts and Flaps, call 911 first. The receiving emergency department coordinates urgent transfer to the nearest hospital hyperbaric programme through the relevant provincial transfer network (CritiCall Ontario at 1-800-668-4357, BC Patient Transfer Network, EHS Nova Scotia, or equivalent). For diving-related emergencies, the Divers Alert Network (DAN) emergency hotline is 1-919-684-9111.

Risks and Contraindications

Untreated pneumothorax is the only absolute contraindication. Concurrent treatment with bleomycin (oxygen-induced pulmonary fibrosis risk) and disulfiram (interference with antioxidant defences) are also contraindicated. Relative contraindications include severe chronic obstructive pulmonary disease with bullous lung disease, uncontrolled seizure disorder, claustrophobia (manageable in monoplace chambers), recent middle-ear or sinus surgery, and uncontrolled hypertension. None of these typically override the hyperbaric decision in a patient with a failing graft or flap that would otherwise require complete revision and a second major operation.

Frequently Asked Questions

HBOT is indicated when a graft or flap shows early signs of compromise (pallor, cyanosis, congestion, capillary refill changes) in the first 24 to 72 hours after surgery, or when a planned reconstruction is to be performed in a compromised recipient site (most commonly previously irradiated tissue). It is an adjunct to surgical management, not a substitute for surgical revision when indicated.

As soon as the diagnosis is recognised, ideally within hours of the appearance of compromise. Twice-daily sessions for the first 24 to 48 hours are standard. Earlier intervention produces better salvage rates. The decision to add HBOT, and whether to combine it with surgical re-exploration of the flap pedicle, is made jointly by the plastic-surgery team and hyperbaric medicine.

Published case series report salvage rates of 65 to 85 percent for compromised grafts and flaps treated with adjunctive HBOT, with the strongest signal in patients treated within hours to a day or two of the index operation. The Cochrane Review concludes HBOT may improve the survival of compromised grafts and flaps, particularly in irradiated tissue.

Yes. Compromised grafts and flaps is recognised by Health Canada and covered at the 11 hospital-based hyperbaric programmes under OHIP, MSP, AHCIP, RAMQ, MSI, MCP, and Saskatchewan Health. Select eligible Independent Health Facilities in Ontario may also bill OHIP for approved indications.

The Marx 20-and-10 protocol is a pre-operative HBOT regimen designed to support reconstructive surgery in previously irradiated tissue. It delivers 20 HBOT sessions before the planned graft or flap and 10 sessions afterward, each at 2.0 to 2.4 ATA for 90 minutes. The pre-operative phase stimulates angiogenesis in the irradiated recipient bed, raising capillary density to approximately 75 to 80 percent of non-irradiated baseline before the surgery. The post-operative phase supports the graft during the critical pre-vascularisation window. The protocol was established by Marx in the 1980s and remains the canonical regimen for head-and-neck reconstruction in irradiated jaws.

No. HBOT is an adjunct to plastic-surgery management. When surgical revision (release of a constricting suture, re-anastomosis of a thrombosed pedicle, drainage of a hematoma compromising perfusion) is indicated, surgery is performed first; HBOT is added afterward to support the revised flap. The decision is made jointly by the plastic-surgery team and hyperbaric medicine.

Typical post-operative rescue course is 10 to 20 sessions: twice-daily for the first 24 to 48 hours, then once-daily for the remainder. Pre-operative Marx 20-and-10 protocol totals 30 sessions over approximately six weeks (20 before surgery, 10 after).

Yes. Replantation of an avulsed segment is one of the recognised acute traumatic ischemia indications, and HBOT supports tissue survival in the marginally perfused replanted segment during the critical period before robust microvascular recovery. Standard adjunctive protocol applies; total course depends on segment size, vascular repair quality, and clinical course.

You change into cotton scrubs, enter the chamber, and lie down (in a monoplace) or sit in a recliner (in a multiplace with multiple patients). Pressurisation takes five to ten minutes and feels like the descent in an aircraft. Most people clear their ears with the same technique used in flying. During the 90-minute treatment phase you breathe pure oxygen, often through a hood or mask. Decompression takes another five to ten minutes. The most common sensation during a session is a feeling of warmth.

All 11 Canadian hospital hyperbaric programmes accept compromised-graft and compromised-flap referrals from plastic-surgery teams. The Canada Hyperbarics verified directory at canadahyperbarics.ca/facilities/ lists all programmes with phone numbers, addresses, and current operational status. Toronto General Hospital has particularly close working relationships with the GTA reconstructive plastic-surgery teams.

Last reviewed: April 28, 2026 | Reviewed by: Canada Hyperbarics Editorial Team | Editorial process | Research sources | Counts & methodology

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