DogNot an appropriate use

Intervertebral Disc Disease (IVDD)

Slipped disc, Herniated disc, Disc extrusion (Hansen type I), Disc protrusion (Hansen type II), Thoracolumbar intervertebral disc extrusion (TL-IVDE), Cervical disc disease (neck IVDD)

Intervertebral disc disease, or IVDD, means one of the soft cushions between the bones of your dog's spine has pushed out of place and is pressing on the spinal cord. That pressure hurts, and it can make the legs weak, wobbly, or unable to move at all. There are two patterns. The sudden kind (disc extrusion, Hansen type I) usually comes on fast, often within a day, and is most common in dogs built with long backs and short legs, such as Dachshunds and French Bulldogs; that is the kind this page is mainly about. The slow kind (disc protrusion, Hansen type II) builds up over weeks to months in older, longer-legged dogs such as German Shepherds, and looks more like a dog who is gradually stiffer, slower on stairs and sore in the back. A disc can also go in the neck rather than the back, and then the front legs are affected too. Most dogs who can still walk do get better. For dogs that are already paralysed the odds depend heavily on the neurologic grade and on whether they have surgery - some of those published numbers are much lower, and for a dog that has lost deep pain sensation in the back feet medical management alone succeeds in only about 1 in 5, versus about 3 in 5 with surgery - so ask your veterinarian for the numbers for YOUR dog. How quickly you are seen matters a great deal: a dog who suddenly cannot walk needs a veterinarian today, not tomorrow. Three things to know before you do anything else. First, NEVER give your dog human pain medicine. Ibuprofen, naproxen, aspirin and acetaminophen (paracetamol) all cause stomach ulcers, bleeding, perforation, kidney failure or liver failure in dogs at doses owners think are harmless - if the pain is not controlled, phone the clinic instead of opening your own medicine cabinet. Second, never give one animal another species' medicine: a dog anti-inflammatory can kill a cat, and the labels of the dog products say so outright. Third, once a drug has been dispensed, call before you change anything - do not add, stop, double up, or switch to something you have at home without speaking to the clinic first, and tell every new veterinarian exactly what your dog has already had, including any steroid injection given elsewhere. And be careful how you move your dog: support the whole body along its length, keep the back in a straight line, never lift under the belly alone, do not let the dog jump down from the car or the sofa, and use a harness rather than a neck collar if the neck is the problem.

What you might notice

  • Crying out, yelping or flinching when you pick your dog up or touch along the back or neck
  • A hunched or arched back, a tense belly, or holding the head low and stiff
  • Suddenly not wanting to jump, use stairs, or get on the couch - or, in the slow form, gradually becoming stiffer and slower over weeks to months
  • Wobbly back legs, scuffing the toenails, crossing the back legs, or knuckling over
  • Dragging the back end, or not able to stand or walk on the back legs at all
  • If the disc is in the neck: neck pain and a low, stiff head carriage, a yelp when the neck is moved, limping or 'root signature' where one front leg is held up, wobbliness or weakness in the FRONT legs as well as the back, or being down on all four legs
  • A tail that hangs limp and does not wag
  • Not able to pee on their own, a firm swollen belly, or urine leaking out
  • Soiling without seeming to know it, a limp open back end, or losing control of bowel movements
  • Trembling, panting, hiding, restlessness or going off food - in dogs these are pain signs

Standard of care

  1. Grade the dog first - everything else follows from the neurologic grade

    Approved / guideline-backed

    Assign severity (spinal pain only, ambulatory paraparesis, non-ambulatory paraparesis, paraplegia DPP, paraplegia DPN) and localise the lesion before discussing options or prices with the owner. The ACVIM panel's outcome table by grade is the single most useful clinical decision tool in this disease, and it only works if the grade is accurate. Give the owner the two numbers for their dog's grade in plain language - the grade-specific prognosis is the information the person funding surgery, or considering euthanasia, most needs, and withholding it to the clinician tier is not honesty.

    ACVIM consensus statement, systematic review of the post-1983 literature; recommendations by grade supported by low to high-level evidence depending on the grade. The panel's own summary states that 'Most recommendations made by the panel were supported by a low or moderate level of evidence' (dog).

    Olby NJ, Moore SA, Brisson B, Fenn J, Flegel T, Kortz G, Lewis M, Tipold A. ACVIM consensus statement on diagnosis and management of acute canine thoracolumbar intervertebral disc extrusion. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480

  2. Surgical decompression for paraplegic dogs, and especially for dogs that have lost deep pain perception

    Approved / guideline-backed

    Published success by grade, medical versus surgical (ACVIM Table 3): spinal pain only and ambulatory paraparesis 80% (115 dogs) vs 98.5% (336 dogs); non-ambulatory paraparesis 81% (131 dogs) vs 93% (341 dogs); paraplegia deep-pain-positive 60% (67 dogs) vs 93% (548 dogs); paraplegia deep-pain-negative 21% (48 dogs) vs 61% (502 dogs). ACVIM verbatim for DPN dogs: 'In paraplegic DPN dogs, success with medical management is largely poor with an increase in the frequency of PMM. Surgical management is recommended.' Also verbatim: 'Surgical treatment should not be declined simply because the dog has been paralyzed for an extended period, because the literature documents that recovery of ambulation may occur for dogs that present with DPN status and have been paralyzed > 1 week before surgery.' That quote must never be presented alone, because on its own it reads as permission to wait, and the panel itself says the two questions are separate: 'The influence of surgical timing on locomotor outcome should be considered independently of its influence on development of PMM.' On the PMM clock, delay is a measured risk - in 197 dogs with complete sensorimotor loss, surgery more than 12 hours after loss of ambulation was associated with PMM (OR 3.4, CI 1.1-10.5, p = 0.03 for 12-24 h; OR 4.6, CI 1.3-16.6, p = 0.02 for >24 h, versus 12 h or less), and disc extrusion at the lumbar intumescence was also associated with PMM (OR 3.02, CI 1.3-7.2, p = 0.01) (Castel et al., BMC Vet Res. 2019;15(1):433, PMID 31796017, DOI 10.1186/s12917-019-2186-0). So: a long-standing paralysis is not a reason to decline surgery, and it is also not a reason to take your time. Hemilaminectomy is the standard approach. On durotomy: one retrospective series reported dogs undergoing durotomy 3.32 times more likely to regain ambulation, with 0% progressive myelomalacia versus 21.5% after hemilaminectomy alone (the consensus reports the two group sizes inconsistently between its own sections, 51 and 65, so no group size is asserted here), and a prospective cohort of 26 paraplegic DPN dogs treated by laminectomy and durotomy reported 16 of 22 followed up (72%) regaining independent ambulation with 1 (5%) developing PMM. These are single-centre, uncontrolled or retrospective figures, and the ACVIM panel makes NO recommendation for or against durotomy - it lists 'impact of durotomy on locomotor outcome and development of progressive myelomalacia' among its areas of high need for further study. Do not read the encouraging numbers as a recommendation, and do not ask a surgeon for a durotomy on the strength of them.

    Named products: Not a drug intervention. Perioperative analgesia is covered in the analgesia step below. For brachycephalic dogs, especially French Bulldogs, the anaesthetic and recovery plan is a separate conversation with the anaesthesia team; the consensus also notes a retrospective association between prolonged anaesthetic time and worse neurologic outcome in paraplegic DPN dogs.

    For paraplegic DPP dogs the consensus recommendation carries the label 'Supported by moderate-level evidence'; for paraplegic DPN dogs the label is 'Supported by moderate to high-level evidence' (both verified against the recommendation boxes in the published consensus). The panel's overall summary nonetheless states that most of its recommendations were supported by a low or moderate level of evidence, and the underlying data are observational studies pooled by systematic review, not randomised trials. The durotomy figures inside this step are NOT graded recommendations and carry no evidence level (dog).

    Olby NJ et al. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480; Castel A, Olby NJ, Ru H, Mariani CL, Munana KR, Early PJ. Risk factors associated with progressive myelomalacia in dogs with complete sensorimotor loss following intervertebral disc extrusion: a retrospective case-control study. BMC Vet Res. 2019;15(1):433. PMID 31796017. DOI 10.1186/s12917-019-2186-0

  3. Multimodal analgesia - and NSAIDs rather than steroids

    Approved / guideline-backed

    For medically managed dogs the ACVIM options are an NSAID, gabapentin or pregabalin for neuropathic pain, and possibly a muscle relaxant such as methocarbamol or diazepam; dogs whose pain requires opioids should be hospitalised until pain is controlled. The recommended postoperative protocol is IV or SC opioids for 24-48 hours (longer if needed), a fentanyl patch for 3-5 days, and an NSAID for 7 days, with pregabalin q8h as a possible addition. Honesty note: in one RCT (n=63) adjunctive gabapentin 10 mg/kg q12h gave no benefit over placebo for 5 days postoperatively, so gabapentin is a reasonable option, not a proven one; the consensus says a q8h interval 'might be beneficial, although evidence to support that assumption currently is lacking'. Two non-negotiables whenever an analgesic goes home with an owner. (1) Never combine an NSAID with a corticosteroid, and never let a dog receive an NSAID in the days after a steroid was given elsewhere without the prescribing veterinarian knowing about it and deciding on a washout - every US canine NSAID label carries this instruction in some form. (2) Owners must be told, in writing, not to supplement with human analgesics and not to give the dog a medicine dispensed for another animal, and to phone before changing any dose.

    Named products: Five NSAID-class analgesics are approved by the US FDA for use in DOGS: carprofen (Rimadyl), meloxicam (Metacam), deracoxib (Deramaxx), firocoxib (Previcox) and grapiprant (Galliprant, an EP4 prostaglandin receptor antagonist, mechanistically distinct from COX inhibitors). NONE of them is approved for intervertebral disc disease or acute spinal pain, so use in IVDD is extra-label BY INDICATION for all five - the same extra-label caveat that applies to gabapentin, pregabalin, methocarbamol and diazepam (which additionally have no canine approval at all, and are therefore extra-label by drug as well). Label indications, verified against the current US labels: carprofen - 'indicated for the relief of pain and inflammation associated with osteoarthritis and for the control of postoperative pain associated with soft tissue and orthopedic surgeries in dogs'; firocoxib - 'the control of pain and inflammation associated with osteoarthritis and for the control of postoperative pain and inflammation associated with soft-tissue and orthopedic surgery in dogs'; deracoxib - osteoarthritis pain and inflammation plus postoperative pain following orthopedic and dental surgery; meloxicam oral suspension - 'the control of pain and inflammation associated with osteoarthritis in dogs' ONLY; grapiprant - 'the control of pain and inflammation associated with osteoarthritis in dogs' ONLY, with no acute-pain or postoperative-pain indication, which makes it the weakest of the five for a step about acute and perioperative spinal pain. Label contraindications and limits: each is contraindicated in dogs with known hypersensitivity to that drug; every label directs that concomitant use with other NSAIDs or corticosteroids be avoided, and the firocoxib label names the drugs explicitly - 'PREVICOX should not be given with other NSAIDs (for example, aspirin, carprofen, etodolac, deracoxib, meloxicam, or tepoxalin) or corticosteroids (for example, prednisone, cortisone, dexamethasone, or triamcinolone)'; the grapiprant label likewise states it 'should not be used with other NSAIDs or corticosteroids'. Age and weight limits: safe use of carprofen has not been established in animals less than 6 weeks of age, in pregnant, breeding or lactating dogs; deracoxib has not been evaluated in dogs younger than 4 months, in breeding, pregnant or lactating dogs; meloxicam oral suspension has not been evaluated in dogs younger than 6 months; firocoxib cannot be accurately dosed in dogs weighing less than 12.5 lb (5.7 kg); grapiprant cannot be accurately dosed in dogs weighing less than 8 lb - which matters in exactly this breed population. Species limits are on the labels too: carprofen states 'For use in dogs only. Do not use in cats'; meloxicam states 'Do not use METACAM Oral Suspension in cats' and carries a boxed warning that 'Repeated use of meloxicam in cats has been associated with acute renal failure and death. Do not administer additional injectable or oral meloxicam to cats'; deracoxib is for oral use in dogs only and is not to be used in cats. These are US FDA approvals only - approval status, product names and permitted indications differ in the EU, the UK, Colombia and elsewhere, so never write 'approved' without naming the regulator. Specific NADA numbers were NOT verified in this research pass and must be confirmed against animaldrugsatfda.fda.gov before any are published on a product or protocol page.

    Medical-management analgesia supported by low-level evidence; postoperative protocol supported by RCT-level evidence for individual components. In 88 dogs with presumptive cervical disc herniation managed medically, NSAID administration was associated with success (P = .035, OR 2.52) (dog).

    Olby NJ et al. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480; Levine JM, Levine GJ, Johnson SI, Kerwin SC, Hettlich BF, Fosgate GT. Evaluation of the success of medical management for presumptive cervical intervertebral disk herniation in dogs. Vet Surg. 2007;36(5):492-9. PMID 17614931. DOI 10.1111/j.1532-950X.2007.00296.x; US FDA-approved labels for Rimadyl (carprofen), Metacam (meloxicam) Oral Suspension, Deramaxx (deracoxib), Previcox (firocoxib) and Galliprant (grapiprant), as published on DailyMed

  4. Do NOT use corticosteroids routinely in the acute phase

    Approved / guideline-backed

    ACVIM verbatim: 'Corticosteroids are not recommended for routine use in medical management of the acute phase of presumptive TL-IVDE. In the chronic phase, a short course of anti-inflammatory doses of corticosteroids may be of benefit for some dogs.' In 223 dogs managed medically for presumptive thoracolumbar disc herniation, glucocorticoid administration was negatively associated with treatment success (P = .008, OR 0.48) and with owner-assessed quality of life (P = .004, OR 0.48). Methylprednisolone sodium succinate and dexamethasone are both listed by the panel among neuroprotective strategies not currently recommended for routine use. This is a negative recommendation and it must be stated as plainly on a client-facing page as on a clinician-facing one, and in Spanish as plainly as in English. It also has a practical corollary for the common real-world sequence in which a primary-care visit gives a steroid injection and the referral centre then adds an NSAID: ask explicitly what has already been given, record it, and do not stack the two.

    Named products: Named agents NOT recommended for routine use: dexamethasone, methylprednisolone sodium succinate (MPSS). Fatal colonic perforations have been described in dogs treated with high doses of dexamethasone, and dogs treated with dexamethasone are more likely to develop urinary tract infections and diarrhoea than dogs given other or no glucocorticoids.

    Supported by moderate-level evidence (ACVIM). Underlying data are retrospective with owner-questionnaire follow-up. One retrospective case-control study of dogs with complete sensorimotor loss reported corticosteroid treatment as negatively associated with PMM (OR 3.1, CI 1.3-7.6, p = 0.01) and its authors concluded that corticosteroid use 'warrants further investigation' - this is a single unreplicated observational signal in one direction against a graded negative recommendation in the other, and it does not license routine steroid use (dog).

    Olby NJ et al. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480; Levine JM, Levine GJ, Johnson SI, Kerwin SC, Hettlich BF, Fosgate GT. Evaluation of the success of medical management for presumptive thoracolumbar intervertebral disk herniation in dogs. Vet Surg. 2007;36(5):482-91. PMID 17614930. DOI 10.1111/j.1532-950X.2007.00295.x; Castel A et al. BMC Vet Res. 2019;15(1):433. PMID 31796017. DOI 10.1186/s12917-019-2186-0

  5. At least four weeks of strict activity restriction

    Approved / guideline-backed

    ACVIM verbatim: 'A least 4 weeks of restricted activity is recommended, putatively to promote healing of the annulus fibrosus. This period should include confinement to a restricted area (crate ideally, or a small room without furniture) except for when performing rehabilitation exercises or outdoor toileting. There should be no off-leash walking, no jumping on or off furniture and no access to stairs during this time.' The same four weeks is recommended after surgery. Be honest with owners about the evidence: in 223 medically managed dogs, duration of restricted activity from none to more than 4 weeks was not associated with outcome, and the panel graded this recommendation as low-level evidence. Activity restriction does not mean skipping rehabilitation exercises. Include handling instruction in the same conversation, because most of the risk in this period is in how the dog is picked up and put down: support the trunk along its whole length, keep the spine in line, never lift under the abdomen alone, lift in and out of the car and off furniture rather than letting the dog jump, and for a cervical lesion walk in a harness rather than a neck collar.

    Supported by low-level evidence (ACVIM consensus agreement rather than trial data) (dog).

    Olby NJ et al. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480

  6. Bladder management and urinary tract infection vigilance

    Approved / guideline-backed

    Retention incontinence is a core component of the disease, not a side issue, and recovery of bladder function lags behind the return of voiding. Reported time to urination by grade: ambulatory paraparesis 1.9 days, non-ambulatory paraparesis 2.9 days, paraplegia DPP 6 days, paraplegia DPN 15.5 days. Cystometry shows maximum bladder pressure and leak-point pressure still abnormal at 42 days. A dog that has started to void has not necessarily recovered normal bladder function - check residual volumes rather than assuming. Owner-side, two things must be taught rather than assumed: manual expression is only done by an owner who has been shown the technique on their own dog by a veterinarian or nurse, because forceful expression risks bladder rupture; and the owner needs the signs of urinary tract infection in plain words (foul, bloody or cloudy urine, straining, discomfort, fever, new leaking) because retention is what predisposes to it.

    Prospective and retrospective cohort studies summarised in the ACVIM consensus statement; no randomised data (dog).

    Olby NJ et al. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480

  7. Basic rehabilitation - and do not oversell intensive rehabilitation

    Approved / guideline-backed

    ACVIM verbatim: 'At a minimum, a basic rehabilitation protocol can be recommended to include cryotherapy, PROM, massage, assisted standing and walking, which can be performed with no specialized equipment or training.' Two RCTs showed that in-hospital, staged, intensive physical rehabilitation for 10-14 days postoperatively is well tolerated but does NOT improve recovery of ambulation compared with basic passive range of motion and assisted walking. Rehabilitation can safely start as early as 24 hours postoperatively; hydrotherapy or underwater treadmill from 3 days (with incision protection) to 14 days. A clinic selling an intensive rehabilitation package should know that the controlled evidence does not support it as superior to the basic protocol.

    Inclusion of basic exercises supported by moderate-level evidence; superiority of intensive protocols contradicted by 2 RCTs (dog).

    Olby NJ et al. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480

  8. Fenestration of the herniated disc at surgery, and consideration of prophylactic fenestration in predisposed breeds

    Approved / guideline-backed

    ACVIM verbatim: 'Fenestration of the herniated disc space at the time of surgical decompression is recommended to minimize risk of recurrence at the site of herniation.' On adjacent discs, verbatim: 'Fenestration of adjacent, degenerated but non-ruptured disc spaces, should be considered. In breeds predisposed to IVDE such as dachshunds and French bulldogs, fenestration is recommended even if the discs are not mineralized.' Reported recurrence was 17.89% with single-site fenestration and 7.45% with multiple-site fenestration; recurrence at new disc spaces is reported in up to 19% of all dogs undergoing decompression, with breed-specific rates of 25% for Dachshunds and 44% for French Bulldogs, and most (87.5%) of these late recurrences develop within 1 to 2 disc spaces of the original extruded disc. Recurrence after medical management ranges from 15% to 66%. The trade-offs the panel names are additional surgical trauma, increased anaesthetic time and cost, plus reported complications including extrusion of additional disc material, potential vertebral instability, increased morbidity at L5-6 and L6-7, and pneumothorax or haemothorax.

    Supported by moderate-level evidence (ACVIM); retrospective comparative data (dog).

    Olby NJ et al. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480

  9. Weight control and sensible lifestyle counselling

    Early evidence

    Overweight dogs had 1.67 times the adjusted odds of owner-reported IVDD (95% CI 1.38-2.01) in 43,517 US dogs. In the same study, higher daily active time, being fed a commercial diet, and regular use of a staircase were associated with REDUCED odds. The staircase finding is counter-intuitive and cross-sectional - it is an association in owner-reported data, plausibly reflecting that dogs already unwell avoid stairs, and it must not be published as advice to make a Dachshund use stairs. What is defensible is weight control, which is also the one modifiable factor with a coherent mechanism and a supporting nutritional guideline.

    Cross-sectional observational association only; no interventional trial of weight loss for IVDD prevention or outcome was located (dog).

    Wee C, Nin DZ. J Am Vet Med Assoc. 2025;263(5):1-9. PMID 39813820. DOI 10.2460/javma.24.08.0553; AAHA Nutrition and Weight Management Guidelines for Dogs and Cats. J Am Anim Hosp Assoc. 2021. PMID 34228790. DOI 10.5326/JAAHA-MS-7232

  10. Breeding and screening advice for predisposed breeds

    Early evidence

    For breeders, this is the only genuinely preventive lever identified. Radiographic screening for intervertebral disc calcification plus 12-FGF4 retrogene genotyping is feasible and the calcification count correlates with overall MRI-graded disc degeneration; 24-48 months of age is a suitable screening age. In 193 radiographically screened Finnish Dachshunds that had reached at least 10 years of age, an owner questionnaire reported clinical IVDD in 31%, strongly associated with calcification grade (P < 0.001) - a single cross-sectional survey of older screened dogs, not a prospective follow-up.

    Prospective blinded imaging study (n = 21 asymptomatic Dachshunds, 546 discs) plus a cross-sectional owner questionnaire (n = 193 Dachshunds aged at least 10 years at the time of the single survey); no breeding-program outcome trial (dog).

    Reunanen VLJ, Jokinen TS, Hytonen MK, Junnila JJT, Lappalainen AK. Acta Vet Scand. 2023;65(1):42. PMID 37752484. DOI 10.1186/s13028-023-00702-0; Lappalainen AK, Vaittinen E, Junnila J, Laitinen-Vapaavuori O. Acta Vet Scand. 2014;56(1):89. PMID 25523328. DOI 10.1186/s13028-014-0089-4

Professional guideline

ACVIM consensus statement on diagnosis and management of acute canine thoracolumbar intervertebral disc extrusion — American College of Veterinary Internal Medicine (ACVIM)

Olby NJ, Moore SA, Brisson B, Fenn J, Flegel T, Kortz G, Lewis M, Tipold A. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480

How it is diagnosed

  • Full neurologic examination to localise the lesion (T3-L3 versus L4-S3, or cervical) and to assign a severity grade: spinal pain only / ambulatory paraparesis / non-ambulatory paraparesis / paraplegia with deep pain perception (DPP) / paraplegia without deep pain perception (DPN). This grade, not the imaging, is what drives prognosis and the surgical decision (Olby et al. 2022, PMID 35880267).
  • Deliberate, careful assessment of deep pain perception (nociception) as a distinct test - a limb withdrawal reflex is not the same as conscious perception, and the DPP/DPN distinction separates an approximately 93% surgical success rate from approximately 61%.
  • Rule out the mimics before committing to a disc diagnosis: acute non-compressive nucleus pulposus extrusion (ANNPE), ischaemic myelopathy / fibrocartilaginous embolism, vertebral fracture or luxation and other trauma, discospondylitis, spinal neoplasia and aortic thromboembolism. Take a deliberate trauma history, because a fracture or luxation changes handling and immobilisation before it changes anything else. In 123 dogs with suspected IVDE managed on clinical reasoning alone at one referral hospital, 81% had a successful outcome without imaging, but 3% proved to have an alternative diagnosis or were euthanised (Scalia & Freeman, Animals. 2024;14(7):1017, PMID 38612256).
  • Advanced imaging when surgery is on the table or the diagnosis is unclear. ACVIM verbatim: 'When extruded material is mineralized, especially in young to middle-aged adult, chondrodystrophic dogs, CT is sensitive in diagnosis and treatment planning. It therefore can be recommended as a first-line advanced imaging modality when acute TL-IVDE is suspected.' MRI (diagnostic sensitivity >98.5%) is preferred where intramedullary lesion definition, prognostication, or a non-IVDE diagnosis matters; minimum sequences are T2W sagittal and transverse.
  • Survey spinal radiographs cannot confirm an extrusion, but they screen for discospondylitis, fracture and vertebral neoplasia and allow counting of mineralised discs.
  • Baseline bloodwork and urinalysis before NSAIDs and general anaesthesia; urine culture if there is retention or a catheter, because retention incontinence predisposes to urinary tract infection.
  • Serial re-examination rather than a single assessment, starting at presentation. Progressive myelomalacia was already evident at first evaluation in 17 of 51 dogs, declared within 48 hours in 25 of 51, and began as late as 5 days after presentation in the remainder (Castel & Olby, PMID 28961348); the ACVIM consensus states that it 'usually develops within days (24 hours up to 14 days) of an acute IVDE-associated injury' and 'is not always apparent at time of presentation'. Read those two together rather than as an interval in which the first day is safe. Signs to actively re-check include cranial advancement of the cutaneous trunci reflex cut-off, loss of patellar reflexes, weak anal tone, loss of abdominal tone, Horner syndrome, thermodysregulation and hypoventilation.

Where a biologic fits

Not an appropriate useNot an appropriate use

Our own product, graded by the same rule

For canine intervertebral disc disease there is no defensible role for stem cell, exosome or peptide products: nothing of the kind has ever been tested in acute thoracolumbar disc extrusion, the nearest canine evidence - a 6-dog pilot of intradiscal stem cells in chronic lumbosacral disc disease - found no clinical benefit and worsening disc degeneration in all three treated dogs, no exosome or peptide product has any published in-vivo clinical efficacy evidence in dogs for this condition, and time spent on an unproven injection is time taken from the two things that do change outcomes - prompt pain control and, for a dog that has lost deep pain perception, prompt decompressive surgery.

What exists

Scope determines the answer here, so state it first. This page is about acute Hansen type I thoracolumbar disc extrusion. NO cell, exosome or peptide product has been tested at all in that disease, so the honest position for acute TL-IVDE is 'no evidence of benefit in either direction' - not 'tested and shown not to work'. What does exist is intradiscal MSC work in a DIFFERENT canine disc disease - chronic degenerative LUMBOSACRAL disc disease with low back pain - and that work was negative on structural endpoints. A neighbouring-disease negative is weaker than a same-disease negative and must not be sold as one, but it is also not encouraging. (1) Steffen et al. 2017: a 6-dog pilot in German Shepherd Dogs with naturally occurring degenerative IVD disease, 3 given intradiscal autologous bone-marrow MSC and 3 intradiscal saline after decompressive surgery, followed 12 months with disc height index, Pfirrmann grading and volumetry of the L7-S1 disc - i.e. lumbosacral, in a non-chondrodystrophic breed. It is the only controlled canine intradiscal MSC study located in this research, but the title is 'Feasibility, Safety, and Preliminary Results' and the conclusion is prefaced 'On the basis of this preliminary study', so it is a pilot rather than a trial and should be read as hypothesis-generating. Authors verbatim: intradiscal autologous MSC 'is well tolerated without any adverse effects, does not affect clinical outcome, and does not have any evident regenerative effects,' and 'In the MSC group, the Pfirrmann grade increased in all patients over time, whereas in the control group, the Pfirrmann grade remained stable.' Concretely, that means disc degeneration grade worsened in all 3 treated dogs and in none of the 3 controls - three dogs per arm (Tissue Eng Part C Methods. 2017;23(11):643-51, PMID 28471303, DOI 10.1089/ten.TEC.2017.0033). (2) Steffen et al., published online 2018 and in issue 2019 (cite as Cell Transplant. 2019;28(2):201-11, PMID 30488736, DOI 10.1177/0963689718815459): 20 client-owned dogs with spontaneous degenerative LUMBOSACRAL IVD disease and low back pain, again not thoracolumbar extrusion; MSC-microcarriers (n = 11), MSC-TGF-beta1-microcarriers (n = 6), microcarriers only (n = 3). Clinical function improved in all groups, but authors verbatim: 'postoperative Pfirrmann grade remained identical in all dogs,' 'microcarriers and MSC failed to regenerate the structure of degenerated IVD,' and Schmorl's node formation was detected in 45% of dogs, falling to 11% when the injection volume was halved - i.e. a procedure-related harm signal, in a study whose control arm was 3 dogs. (3) Kim et al. 2016, 34 dogs with acute thoracolumbar IVDD and absent deep pain perception, all decompressed within a week, with adipose-derived MSC transplanted into the injured cord parenchyma in a treatment subgroup; reported better recovery than decompression alone, but with no reported group sizes, allocation method or blinding, and intraparenchymal cord injection is a materially higher-risk procedure than intradiscal or IV delivery (J Vet Sci. 2016;17(1):123, PMID 27051350, DOI 10.4142/jvs.2016.17.1.123). Because 21% to 61% of DPN dogs recover with conventional care alone, an unblinded comparison at this grade is fragile. (4) Besalti et al. 2015: 7 paraplegic DPN dogs, uncontrolled case series, neurogenically induced autologous BM-MSC injected percutaneously into the cord; at 2 months only 1 dog improved by 1 gait-score point (Turk Neurosurg, DOI 10.5137/1019-5149.JTN.14502-15.2). (5) A 2024 review of 45 companion-animal stem cell studies (2015-2023) found only 12 were randomised and controlled, and specifically noted that the exceptions to generally beneficial reports were 'those related to more chronic processes such as spinal cord injury and chronic kidney disease' (Williams ZJ, Pezzanite LM, Chow L, Rockow M, Dow SW. Stem Cells. 2024;42(8):677-705, PMID 38795363, DOI 10.1093/stmcls/sxae034). (6) The ACVIM consensus panel stated verbatim: 'Evaluation of cell-based treatments was considered beyond the scope of this discussion' - so no guideline endorses them here, and no guideline has rejected them here either. (7) On the exosome/EV side, the canine-relevant work is in vitro or in the wrong species: notochordal-cell-derived EVs raised glycosaminoglycan deposition in canine and human nucleus pulposus cell micro-aggregates in culture (Bach et al., Oncotarget. 2017;8:88845-56, PMID 29179481, DOI 10.18632/oncotarget.21483), and canine MSC-derived EVs improved locomotor recovery in RATS with spinal cord injury, which its own title states honestly (Nishida et al., Regen Ther. 2025;30:164-72, PMID 40575347, DOI 10.1016/j.reth.2025.05.014). (8) Bone marrow aspirate concentrate in ultra-purified alginate gel suppressed disc degeneration after discectomy in an experimentally induced canine model at 24 weeks - a preclinical proof-of-concept in laboratory dogs with surgically created lesions, explicitly not naturally occurring clinical disease (Ukeba et al., Cells. 2024;13(11):987, PMID 38891119, DOI 10.3390/cells13110987). (9) Jurisdiction, since it is routinely blurred: the one MSC product authorised for dogs anywhere is DogStem, which is EQUINE umbilical cord-derived MSC authorised for dogs by the EUROPEAN MEDICINES AGENCY (EMEA/V/C/005829, marketing authorisation holder EquiCord S.L.), and its authorised indication is osteoarthritis - not disc disease, not spinal cord injury. Its supporting canine RCT (Punzon et al., J Am Vet Med Assoc. 2022;260(15):1947-55, PMID 36198051, DOI 10.2460/javma.22.06.0237, n = 80 client-owned dogs, intra-articular, manufacturer-authored) is an osteoarthritis trial. There is no FDA approval of DogStem or of any other animal cell or exosome product in the United States, and an EU authorisation for one indication in one joint is not evidence for a different disease in the spine.

What has not been shown

There is no randomised controlled trial - adequately powered or otherwise - of any cell, exosome or peptide product for acute canine thoracolumbar disc extrusion. Total dogs in genuine placebo/control arms across the entire canine intradiscal MSC literature located is six (3 MSC vs 3 saline in the Steffen 2017 pilot) plus a 3-dog control arm in Steffen 2019, and all of those dogs had lumbosacral rather than thoracolumbar disease. There is no published in-vivo clinical efficacy study of exosome or extracellular vesicle products in dogs or cats for IVDD or for spinal cord injury of any cause - the relevant EV work is in vitro or in rats. There is no controlled canine clinical trial of BPC-157, TB-500 or any other peptide for this or any indication; the only dog data for BPC-157 is a beagle pharmacokinetic study (IM bioavailability 45-51%, elimination half-life under 30 minutes - He L et al., Front Pharmacol. 2022;13:1026182, PMID 36588717, DOI 10.3389/fphar.2022.1026182), which is laboratory pharmacology with no efficacy endpoint in any veterinary species, and thymosin beta-4 (TB-500) is listed as a banned substance in the FEI Equine Prohibited Substances Database under 'Thymosin (synthetic fragments)'. Nothing has been shown to prevent a disc extruding, to restore lost deep pain perception, to regenerate a degenerated canine disc, to reduce progressive myelomalacia, or to substitute for decompressive surgery. There is no analgesic-equivalence evidence against an NSAID. And there is no FDA-approved animal cell- and tissue-based product in the United States: FDA states verbatim that 'Currently, no ACTPs are FDA-approved' and that it is illegal to market an unapproved ACTP. This is not abstract for this condition - FDA's warning letter to Safari Stem Cell, LLC (MARCS-CMS 661023, 5 April 2024) specifically listed 'intervertebral disc disease (IVDD)' among the indications the firm was marketing, quoted the website claim 'Disc Disease/Spinal Cord Injury' back at it, and held that the firm was marketing unapproved new animal drugs. FDA has also written, in a separate letter, that an 'unproven treatment could cause animal owners to forgo or delay appropriate veterinary care' - which in this disease is the whole risk. A Colombian or other non-US entity does not change US marketing law for US-directed promotion. Also non-defensible as a concept: 'immune-privileged', 'immune-invisible' or 'zero-flare' cells. Punzon et al., in a randomised controlled safety trial of intra-articular xenogeneic equine umbilical-cord MSC versus allogeneic canine adipose MSC versus placebo in 24 police working dogs, found that BOTH equine and canine MSC generated antibody titres in the dogs, although no adverse events were detected and the administration was concluded to be safe (Front Vet Sci. 2023;10:1098029, PMID 37266387, DOI 10.3389/fvets.2023.1098029).

Sources

  1. The only controlled canine intradiscal MSC study located - a 6-dog PILOT (3 vs 3) in degenerative LUMBOSACRAL disc disease, not thoracolumbar extrusion; negative, with worsening Pfirrmann grade in all 3 treated dogs — Steffen F, Smolders LA, Roentgen AM, Bertolo A, Stoyanov J. Bone Marrow-Derived Mesenchymal Stem Cells as Autologous Therapy in Dogs with Naturally Occurring Intervertebral Disc Disease: Feasibility, Safety, and Preliminary Results. Tissue Eng Part C Methods. 2017;23(11):643-651. PMID 28471303. DOI 10.1089/ten.TEC.2017.0033 https://doi.org/10.1089/ten.TEC.2017.0033
  2. 20-dog prospective study in degenerative LUMBOSACRAL disc disease (online 2018, in issue 2019); failed to regenerate disc structure, Schmorl's nodes in 45% of dogs, control arm n=3 — Steffen F, Bertolo A, Affentranger R, Ferguson SJ, Stoyanov J. Treatment of Naturally Degenerated Canine Lumbosacral Intervertebral Discs with Autologous Mesenchymal Stromal Cells and Collagen Microcarriers: A Prospective Clinical Study. Cell Transplant. 2019;28(2):201-211. PMID 30488736. DOI 10.1177/0963689718815459 https://doi.org/10.1177/0963689718815459
  3. 34 DPN dogs, unblinded, intraparenchymal AD-MSC; no group sizes or allocation reported — Kim Y, Lee SH, Kim WH, Kweon OK. Transplantation of adipose derived mesenchymal stem cells for acute thoracolumbar disc disease with no deep pain perception in dogs. J Vet Sci. 2016;17(1):123-126. PMID 27051350. DOI 10.4142/jvs.2016.17.1.123 https://doi.org/10.4142/jvs.2016.17.1.123
  4. 2024 review of 45 companion-animal stem cell studies; only 12 randomised and controlled, and spinal cord injury named as an exception to beneficial reports — Williams ZJ, Pezzanite LM, Chow L, Rockow M, Dow SW. Evaluation of stem-cell therapies in companion animal disease models: a concise review (2015-2023). Stem Cells. 2024;42(8):677-705. PMID 38795363. DOI 10.1093/stmcls/sxae034 https://doi.org/10.1093/stmcls/sxae034
  5. Canine and human nucleus pulposus EV work - IN VITRO ONLY, not a treatment study — Bach F, Libregts S, Creemers L, Meij B, Ito K, Wauben M, Tryfonidou M. Notochordal-cell derived extracellular vesicles exert regenerative effects on canine and human nucleus pulposus cells. Oncotarget. 2017;8(51):88845-88856. PMID 29179481. DOI 10.18632/oncotarget.21483 https://doi.org/10.18632/oncotarget.21483
  6. Canine-sourced EVs for spinal cord injury - the recipients were RATS; do not cite as canine evidence — Nishida H, Matsuura H, Yoshizaki K, et al. Sustained release of canine mesenchymal stem/stromal cell-derived extracellular vesicles rescues motor function in rodent spinal cord injury models. Regen Ther. 2025;30:164-172. PMID 40575347. DOI 10.1016/j.reth.2025.05.014 https://doi.org/10.1016/j.reth.2025.05.014
  7. Preclinical canine model (surgically induced lesions, laboratory dogs), BMAC in alginate gel after discectomy — Ukeba D, Ishikawa Y, Yamada K, et al. Bone Marrow Aspirate Concentrate Combined with Ultra-Purified Alginate Bioresorbable Gel Enhances Intervertebral Disc Repair in a Canine Model: A Preclinical Proof-of-Concept Study. Cells. 2024;13(11):987. PMID 38891119. DOI 10.3390/cells13110987 https://doi.org/10.3390/cells13110987
  8. Both equine and canine MSC raised antibody titres in dogs - 'immune-privileged' and 'zero-flare' are not defensible claims — Punzon E, Garcia-Castillo M, Rico MA, Padilla L, Pradera A. Local, systemic and immunologic safety comparison between xenogeneic equine umbilical cord mesenchymal stem cells, allogeneic canine adipose mesenchymal stem cells and placebo: a randomized controlled trial. Front Vet Sci. 2023;10:1098029. PMID 37266387. DOI 10.3389/fvets.2023.1098029 https://doi.org/10.3389/fvets.2023.1098029
  9. The n=80 canine RCT behind DogStem - EQUINE UC-MSC, intra-articular, for OSTEOARTHRITIS; EMA-authorised for dogs (EMEA/V/C/005829), no FDA approval, and not evidence for disc disease — Punzon E, Salguero R, Totusaus X, Mesa-Sanchez C, Badiella L, Garcia-Castillo M, Pradera A. Equine umbilical cord mesenchymal stem cells demonstrate safety and efficacy in the treatment of canine osteoarthritis: a randomized placebo-controlled trial. J Am Vet Med Assoc. 2022;260(15):1947-1955. PMID 36198051. DOI 10.2460/javma.22.06.0237 https://doi.org/10.2460/javma.22.06.0237
  10. Only dog data for BPC-157 - beagle pharmacokinetics, no efficacy endpoint in any veterinary species — He L, Zhou Z, Wang Y, et al. Pharmacokinetics of body protective compound 157 in beagle dogs. Front Pharmacol. 2022;13:1026182. PMID 36588717. DOI 10.3389/fphar.2022.1026182 https://doi.org/10.3389/fphar.2022.1026182
  11. ACVIM panel excluded cell-based treatments from scope; no guideline endorsement and no guideline rejection exists for this indication — Olby NJ, Moore SA, Brisson B, et al. J Vet Intern Med. 2022;36(5):1570-1596. PMID 35880267. DOI 10.1111/jvim.16480 https://doi.org/10.1111/jvim.16480
  12. FDA: no ACTP is FDA-approved; marketing an unapproved ACTP is illegal. The Safari Stem Cell warning letter named IVDD specifically. — US FDA. FDA's Role in Veterinary Regenerative Medicine; CVM GFI #218, Cell-Based Products for Animal Use (June 2015); Warning Letter to Safari Stem Cell, LLC, MARCS-CMS 661023, 5 April 2024. https://www.fda.gov/animal-veterinary/cell-and-tissue-products-a

Tracking response

How you know whether it is working

Open Field Score (OFS) and Texas Spinal Cord Injury Score (TSCIS) for serial gait and neurologic recovery; the modified Frankel Scale (MFS) for coarse grading. In a 20-rater reliability study on video from dogs recovering from IVDD-associated spinal cord injury, intraclass correlation was 0.96 for both OFS and TSCIS and 0.85 for MFS, regardless of rater expertise; MFS and simple binary outcomes showed a marked ceiling effect once dogs regained ambulation, while OFS and TSCIS captured ongoing recovery better.

Olby N, Griffith E, Levine J. Comparison of Gait Assessment Scales in Dogs with Spinal Cord Injury from Intervertebral Disc Herniation. J Neurotrauma. 2020;37(18):1991-1998. PMID 31914849. DOI 10.1089/neu.2019.6804

Suggested cadence: While hospitalised: neurologic re-examination at least daily, and immediately on any owner-reported change; assessment for progressive myelomalacia starts at the first examination, since a third of affected dogs already show signs then. After discharge: owner check-in daily for the first 14 days; clinician re-examination at 2 weeks, at 4-6 weeks (before activity restriction is lifted), and at 3 months. Any deterioration at any point triggers an unscheduled re-examination rather than a wait-and-see.

Questions you can answer at home

  • Today, can your dog stand up and take steps on the back legs without help - none, some with support, or yes on their own?
  • Is the back end getting stronger, staying the same, or getting weaker compared with yesterday?
  • Did your dog pee on their own today? Did you have to help the bladder empty, and did any urine leak between times? Does the urine smell bad, look bloody or cloudy, or is your dog straining?
  • Has your dog passed a bowel movement, and is there any soiling that your dog does not seem to notice?
  • Does your dog cry out, flinch or tense up when picked up, or when you touch along the back or neck?
  • Has any weakness, floppiness or change appeared further forward - in the belly, the front legs, the neck, or in breathing?
  • If your dog is on an anti-inflammatory: any vomiting, blood or coffee-ground material in vomit, black or bloody stool, loss of appetite, extra drinking or urinating, or yellow gums?
  • Have you given your dog anything that we did not dispense - including anything from your own medicine cabinet or prescribed for another pet?
  • Is your dog eating, sleeping and settling normally, and does the day seem comfortable or uncomfortable overall?

Last reviewed: 2026-09-12 · Every claim on this page carries a citation you can check. If one does not hold up, tell us and we will correct it. science@azzamedical.com

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