Hand & Upper Limb

Calcific Tendinitis of the Shoulder

Barbotage and arthroscopic excision of calcific tendinitis - FRCS/FRACS exam preparation guide

Core Procedure
intermediate
By OrthoVellum Medical Education Team

Reviewed by OrthoVellum Editorial Team

Editorial maintenance, source checking, and correction workflow β€’ Published by OrthoVellum Medical Education Team

High-yield overview

Subacromial approach | intermediate

Surgical Imaging

AP shoulder radiograph showing calcium deposit arrow in supraspinatus rotator cuff
AP shoulder radiograph of calcific tendinitis: white arrow identifies a dense, well-circumscribed calcium deposit in the supraspinatus tendon critical zone (1–2cm proximal to the greater tuberosity insertion). The dense homogeneous appearance is consistent with GΓ€rtner Type I (formative phase) β€” though counterintuitively, the less dense Type III (resorptive) deposits cause more acute pain.Credit: Verstraelen FU et al., SpringerPlus 2016 (PMC4769244) β€” CC BY 4.0
Arthroscopic view showing probe in subacromial space with white calcium material visible
Arthroscopic appearance of calcific tendinitis: the subacromial bursa is entered and a probe identifies the calcium deposit bulging through the rotator cuff surface. The white chalky material (calcium hydroxyapatite) is visible extruding into the subacromial space β€” Type III resorptive deposits have this characteristic toothpaste-like consistency that facilitates needle aspiration.Credit: Verstraelen FU et al., SpringerPlus 2016 (PMC4769244) β€” CC BY 4.0
Six-panel arthroscopic sequence showing calcific tendinitis excision from needle puncture to calcium debridement and cuff repair
Arthroscopic calcific tendinitis excision sequence: (A) calcium deposit bulging through cuff surface; (B) needle puncture releases calcium; (C) white calcium material escaping under subacromial pressure; (D) motorised burr debridement of calcium; (E) rotator cuff defect after calcium removal; (F) suture repair of cuff defect greater than 50% tendon thickness. Defects under 25% do not require formal repair.Credit: Rebuzzi E et al., Int Orthop 2008 (PMC2657331) β€” CC BY 4.0

Critical Exam Topics β€” Calcific Tendinitis

GΓ€rtner Classification

Type I β€” Formative/Dense: Dense, homogeneous, sharply defined borders, chalk-like consistency at needling. Often asymptomatic; may be incidental finding. Hard to aspirate.

Type II β€” Transitional: Mixed appearance, partly homogeneous/partly inhomogeneous, intermediate density. Variable symptoms.

Type III β€” Resorptive/Fluffy: Inhomogeneous, fluffy or cloudy margins, toothpaste-like consistency at aspiration. Most symptomatic β€” responsible for acute severe pain. Easiest to aspirate via barbotage.

Barbotage Technique

Setup: Ultrasound-guided, real-time imaging, patient supine or seated, transducer over supraspinatus long-axis.

Technique: Two-needle technique preferred β€” first 18G needle for lavage (saline), second for aspiration. Alternatively: single 18G needle with pulsed saline injection and aspiration cycles. Deposit visualised as hyperechoic focus with posterior shadowing.

End-point: Aspiration of chalky white/toothpaste material; deposit size reduction on US. Local anaesthetic co-injection for pain control. Corticosteroid co-injection optional (reduces post-procedure flare).

When to Operate

Conservative threshold: Minimum 3 months NSAID + physiotherapy failure.

Barbotage threshold: 6 weeks post-barbotage no improvement (or barbotage technically failed β€” Type I hard deposit, failed aspiration).

Absolute surgical indications: Continued severe pain/disability after two barbotage attempts; hard Type I deposit not amenable to aspiration; large deposit with mechanical impingement.

Relative indications: Type II–III with partial response but persistent symptoms. Examiners expect stepwise management β€” do NOT jump to surgery.

Tendon Integrity Assessment

Preoperative: Ultrasound or MRI to assess rotator cuff before surgery β€” document any pre-existing partial or full-thickness tear.

Intraoperative: After calcium debridement, probe residual tendon with hook β€” assess remaining thickness and quality.

Decision threshold: If excision defect is greater than 50% of tendon thickness, formal rotator cuff repair (double-row preferred) is mandatory β€” prevents chronic impingement and progressive tear.

Documentation: Always record pre-excision tendon appearance and post-excision repair type in operative note β€” medicolegally important.

Concomitant SAD Decision

Indication for concurrent SAD: Documented subacromial impingement on imaging (hooked acromion, subacromial spur, positive Hawkins-Kennedy, positive Neer sign) or intraoperative finding of frayed coracoacromial ligament or bursal-sided wear.

Evidence: Routine acromioplasty in isolated calcific tendinitis without structural impingement is not supported β€” the disease is intratendinous, not primarily an extrinsic impingement problem, so completeness of calcium removal (not acromioplasty) drives outcome. Reserve SAD for genuine concomitant impingement.

Technique: Standard arthroscopic acromioplasty β€” resect inferior acromion 5–8 mm using arthroscopic burr. Preserve coracoacromial arch if no impingement.

Rotator Cuff Repair Need

Primary repair: Greater than 50% tendon thickness defect after excision β€” repair with suture anchors (single or double row depending on defect size).

Small defects: Less than 25% tendon thickness β€” debride edges, mark with suture, no repair needed. Heal by secondary intention.

Intermediate defects: 25–50% thickness β€” surgeon discretion based on tissue quality, patient demand, age. Many surgeons repair greater than 33% in younger active patients.

Postoperative restriction: If repair performed, apply standard rotator cuff repair protocol β€” sling 4–6 weeks, no active elevation until week 6, strengthening from week 12.

Mnemonic

GARTNERGARTNER β€” Classification System

Hook:The GΓ€rtner and Heyer radiographic classification is the gold standard used in exams. Examiners expect you to know all three types, their radiographic appearance, and the correlation between type and symptom severity. Type III (resorptive) is highest yield β€” most symptomatic, most amenable to barbotage, and the phase in which spontaneous resolution occurs.

Mnemonic

CALCIUMCALCIUM β€” Management Steps

Hook:CALCIUM drives the entire management pathway β€” from conservative care through to arthroscopic excision. Examiners expect you to follow this stepwise approach and NOT proceed to surgery before exhausting non-operative measures including barbotage.

Epidemiology

Prevalence: Radiographic calcific deposits in roughly 3–8% of adult shoulders, with a higher proportion among symptomatic patients. Peak presentation age 30–60 years. Female slightly predominant. Bilateral in 10–25%. Distinct from degenerative rotator cuff disease β€” patients are typically younger and the cuff is usually intrinsically intact.

Natural history: This is fundamentally a self-limiting reactive (cell-mediated) calcification, not a degenerative process. Deposits cycle through a formative (resting) phase and a resorptive phase; the resorptive phase (GΓ€rtner Type III) is intensely painful but is precisely when spontaneous resolution occurs β€” frequently over a few weeks. Many formative (Type I) deposits persist for years with inconsistent symptoms. Spontaneous resorption is the rule rather than the exception (GΓ€rtner and Heyer 1995, PMID 7617385).

Supraspinatus critical zone: Calcification occurs most commonly in supraspinatus (around 70–80% of cases), classically about 1–2 cm proximal to the greater tuberosity insertion β€” the "critical zone" of relative hypovascularity (Moseley and Goldie 1963). Less common sites: infraspinatus and subscapularis.

Conservative Management

First-line (3 months minimum):

  • NSAIDs (e.g. naproxen 500 mg BD) and physiotherapy (pendulum, ROM, posture correction)
  • Subacromial corticosteroid injection: reduces acute pain, aids physiotherapy engagement
  • Extracorporeal shockwave therapy (ESWT): evidence supports as alternative to barbotage for Type I/II deposits β€” non-invasive, may take 3–4 sessions

Barbotage Indications and Evidence

Indication: Failed conservative therapy greater than 3 months, particularly Type II/III deposits (soft consistency amenable to aspiration).

Evidence: A randomised controlled trial (de Witte et al. 2013, PMID 23696211) showed ultrasound-guided needling and lavage combined with a subacromial corticosteroid injection produced significantly better Constant scores and greater deposit resorption at 1 year than an isolated subacromial corticosteroid injection (mean Constant 86.0 vs 73.9 at 12 months). A Level I network meta-analysis (Arirachakaran et al. 2017, PMID 27554465) ranked barbotage (with subacromial corticosteroid) as the treatment of choice among non-operative options.

Technical success: Aspiration of chalky/toothpaste-like material is achieved more readily in soft resorptive (Type III) deposits; hard, dense formative (Type I) deposits aspirate poorly and are a recognised cause of barbotage failure.

Post-barbotage: Substantial symptomatic improvement and progressive radiographic resorption are usual over 3–12 months. Repeat barbotage is reasonable for partial response before considering surgery.

Surgical Indications

Operative thresholds (all should be met):

  1. Persistent symptoms severe enough to affect quality of life or work
  2. Failed minimum 3 months conservative treatment
  3. Failed at least one barbotage attempt (or technically impossible β€” Type I)
  4. Imaging confirmation of calcium deposit (plain film + US)

Absolute contraindications: Active shoulder infection, uncontrolled medical comorbidities, patient unwilling to commit to postoperative rehabilitation.


Clinical Decision Scenarios

Use these scenarios to practise clinical reasoning and management decisions

CLINICAL SCENARIOStandard

Scenario 1: GΓ€rtner Type I vs Type III β€” Who Needs Surgery?

CLINICAL PROMPT

"A 45-year-old nurse presents with 6 months of right shoulder pain. Plain radiograph shows a 2 cm calcium deposit at the supraspinatus insertion. How do you assess this and decide on management? The radiograph shows a dense, sharply-defined homogeneous opacity. Separately, describe how your approach would differ if the deposit appeared fluffy with indistinct margins."

PRACTICAL APPROACH
This question tests understanding of GΓ€rtner classification and its direct impact on management decisions. Assessing the deposit shown (dense, sharply defined, homogeneous opacity): this is a GΓ€rtner Type I (formative/dense) deposit. Type I deposits are chalk-like in consistency, often asymptomatic, and may represent incidental findings. However, this patient has 6 months of significant symptoms, so the deposit is clinically relevant. My management for Type I: (1) Confirm diagnosis with ultrasound to assess deposit size, depth (bursal vs intatendinous), and rotator cuff integrity. (2) Initiate/continue conservative measures β€” physiotherapy, NSAIDs, subacromial steroid injection. (3) If failed 3 months conservative treatment: consider ESWT (extracorporeal shockwave therapy) as Type I deposits are often hard and may respond to shockwave. Barbotage technically more difficult for Type I (hard/dense, poor aspiration yield) but worth one attempt with image guidance. (4) If failed barbotage or barbotage impossible: surgical referral for arthroscopic excision. Type I deposits may require formal excision more often than Type III because they are harder and less amenable to aspiration. In contrast, if the deposit showed fluffy, inhomogeneous margins with ill-defined borders β€” this is GΓ€rtner Type III (resorptive/fluffy). Type III is the most symptomatic stage, corresponding to the acute resorptive phase. The patient classically describes excruciating pain, often waking at night, disproportionate to any prior trauma. This patient needs urgent barbotage β€” the toothpaste-like consistency of Type III aspirates beautifully. I would expedite ultrasound-guided barbotage, co-inject subacromial steroid for the inevitable post-procedure flare, and expect excellent short-term relief. Surgery is rarely needed for Type III as many resolve spontaneously or respond to barbotage. Key teaching point: Type III most painful but most likely to resolve; Type I less painful acutely but may persist and require surgery. Examiners will test whether you know this counterintuitive relationship.
CLINICAL SCENARIOAdvanced

Scenario 2: Intraoperative Tendon Gap Greater Than 50% β€” What to Do?

CLINICAL PROMPT

"During arthroscopic excision of a large Type I supraspinatus calcium deposit, you excise the deposit and assess the residual tendon. You estimate the defect is approximately 60% of tendon thickness. The patient is a 52-year-old active male with high functional demands. What are your intraoperative and postoperative management decisions?"

PRACTICAL APPROACH
This is a high-stakes intraoperative decision point that tests operative judgment and knowledge of rotator cuff repair principles. With a defect greater than 50% of tendon thickness β€” the threshold for formal repair β€” I must proceed to rotator cuff repair before concluding the procedure. Failing to repair a significant defect risks progressive tear propagation, chronic impingement of the tendon remnant, and poor functional outcome. My intraoperative steps: (1) Thoroughly probe and visualise the defect. Confirm its dimensions β€” AP width (typically 1–2 cm for calcium excision defect), and mediolateral depth (confirm greater than 50% thickness). Document with arthroscopic photographs. (2) Convert lateral portal to primary working portal for suture anchor placement. If working space is limited, add an anterolateral portal. (3) Prepare the greater tuberosity footprint β€” lightly burr the medial row footprint to bleeding cancellous bone for anchor purchase. Do NOT remove excessive bone. (4) Anchor selection and placement: For a defect 1–2 cm wide, a single-row repair with 1–2 suture anchors is generally adequate. For a defect greater than 2 cm, consider double-row (transosseous-equivalent or TOE) repair. Place medial row anchor at articular margin, lateral row anchors at lateral footprint (double row) or a single mid-footprint anchor (single row). (5) Suture passage: Pass sutures through tendon edges in mattress or simple configuration. Mason-Allen equivalent (horizontal mattress + locking) provides superior pull-out strength. (6) Tie sutures with adequate tension β€” arm in neutral rotation. Confirm repair water-tight and no edge lifting. (7) Assess repair tension β€” arm in full adduction should allow repair without gapping; if excessive tension at 30Β° abduction, repair may be at risk. (8) Update anaesthetic team: case extended for cuff repair β€” document repair type in notes. Postoperatively: Apply formal rotator cuff repair rehabilitation protocol β€” sling immobilisation 6 weeks, passive ROM only weeks 0–6, active-assisted weeks 6–12, strengthening from weeks 12–24. Counsel patient postoperatively about the additional repair and adjusted recovery expectations (4–6 months rather than 2–3 months).
CLINICAL SCENARIOStandard

Scenario 3: Six Weeks Post-Barbotage β€” No Improvement

CLINICAL PROMPT

"A 48-year-old teacher underwent ultrasound-guided barbotage six weeks ago for a Type II calcific tendinitis deposit in the supraspinatus. She reports minimal improvement in pain. Follow-up ultrasound shows the deposit is largely unchanged in size and appearance. How do you manage her now?"

PRACTICAL APPROACH
Six weeks with no clinical improvement and unchanged deposit on ultrasound represents a failure of barbotage. My systematic approach: (1) Reassess the clinical picture: confirm pain is from the calcific deposit (subacromial test β€” temporary relief with subacromial injection confirms subacromial source). Exclude red flags β€” significant neurological deficit, unexplained weight loss, disproportionate night pain raising concern for malignancy. (2) Review barbotage technique: was it technically successful? Was there any aspiration? Did the patient have the expected 24–72 hour flare (indicating the procedure reached the deposit)? If no flare and no aspiration, the procedure may not have reached the deposit correctly β€” consider repeat barbotage under fluoroscopic guidance or with a different operator. (3) Review imaging: re-examine the deposit characteristics. Is this actually a Type II or more consistent with Type I (harder, dense)? CT imaging can better characterise deposit density than plain films. A Type I deposit that was misclassified as Type II explains poor barbotage response. (4) Management options at this point: Option A β€” Repeat barbotage: if the first was technically suboptimal (no aspiration, no flare, uncertain needle position), a technically sound second attempt is reasonable. Option B β€” ESWT: high-energy extracorporeal shockwave therapy improves function, reduces pain and diminishes deposit size versus placebo, with high-energy superior to low-energy (Gerdesmeyer et al. 2003 JAMA, PMID 14625334). It is a reasonable non-operative option for refractory deposits, including harder Type I–II, typically delivered over 2 or more sessions a couple of weeks apart followed by physiotherapy. Option C β€” Surgical referral: after two failed barbotage attempts or technically impossible aspiration (hard Type I), refer for arthroscopic excision. Given this is the first barbotage with no response, I would: review technique and consider repeat barbotage or introduce ESWT. If two attempts failed by 3 months, I would refer for arthroscopic excision. Counsel patient that surgical outcomes are excellent (85–90% at 2 years) and that this pathway, while slower, is appropriate and evidence-based.

Calcific Tendinitis β€” Exam Summary

Clinical summary

Key Evidence

Calcific tendinitis of the shoulder β€” radiographic classification and natural history

Level III
GΓ€rtner J, Heyer A β€’ Der OrthopΓ€de
Clinical Implication: The GΓ€rtner type seen on plain film is both a staging and a prognostic tool: hard Type I deposits respond poorly to needling and are over-represented among cases that come to surgery, whereas painful Type III deposits are usually best managed expectantly or with barbotage because they resolve.

Ultrasound-guided needling and lavage versus subacromial corticosteroids: a randomized controlled trial

Level I
de Witte PB, Selten JW, Navas A, Nagels J, Visser CPJ, Nelissen RGHH, Reijnierse M β€’ American Journal of Sports Medicine
Clinical Implication: Ultrasound-guided barbotage combined with a subacromial corticosteroid injection gives superior pain, function and deposit resorption compared with steroid injection alone, supporting barbotage as first-line interventional treatment after failed simple conservative care.

Extracorporeal shock wave therapy for chronic calcifying tendonitis of the rotator cuff: a randomized controlled trial

Level I
Gerdesmeyer L, Wagenpfeil S, Haake M, Maier M, Loew M, WΓΆrtler K, et al. β€’ JAMA
Clinical Implication: High-energy ESWT is an evidence-based non-operative alternative to barbotage, particularly useful for harder Type I–II deposits, and should be considered before surgery in deposits refractory to simpler measures.

ESWT, ultrasound-guided lavage, corticosteroid injection and combined treatment for rotator cuff calcific tendinopathy: a network meta-analysis of RCTs

Level I
Arirachakaran A, Boonard M, Yamaphai S, Prommahachai A, Kesprayura S, Kongtharvonskul J β€’ European Journal of Orthopaedic Surgery & Traumatology
Clinical Implication: Pooled Level I evidence supports a non-operative ladder led by ultrasound-guided barbotage with subacromial corticosteroid, with surgery reserved for genuine treatment failures.

Arthroscopic treatment of calcific tendinitis of the shoulder

Level IV
Ark JW, Flock TJ, Flatow EL, Bigliani LU β€’ Arthroscopy
Clinical Implication: Arthroscopic calcium removal reliably relieves symptoms in chronic resistant disease even when calcium removal is only partial, confirming surgery as an effective last step once non-operative options are exhausted.

References

  1. GΓ€rtner J, Heyer A (1995). Kalkschulter β€” Tendinosis calcarea [Calcific tendinitis of the shoulder]. OrthopΓ€de. 24(3):284–302. PMID: 7617385. (Radiographic classification and natural history)

  2. Ark JW, Flock TJ, Flatow EL, Bigliani LU (1992). Arthroscopic treatment of calcific tendinitis of the shoulder. Arthroscopy. 8(2):183–188. PMID: 1637430. DOI: 10.1016/0749-8063(92)90034-9

  3. de Witte PB, Selten JW, Navas A, Nagels J, Visser CPJ, Nelissen RGHH, Reijnierse M (2013). Calcific tendinitis of the rotator cuff: a randomized controlled trial of ultrasound-guided needling and lavage versus subacromial corticosteroids. Am J Sports Med. 41(7):1665–1673. PMID: 23696211. DOI: 10.1177/0363546513487066

  4. Gerdesmeyer L, Wagenpfeil S, Haake M, Maier M, Loew M, WΓΆrtler K, et al. (2003). Extracorporeal shock wave therapy for the treatment of chronic calcifying tendonitis of the rotator cuff: a randomized controlled trial. JAMA. 290(19):2573–2580. PMID: 14625334. DOI: 10.1001/jama.290.19.2573

  5. Arirachakaran A, Boonard M, Yamaphai S, Prommahachai A, Kesprayura S, Kongtharvonskul J (2017). Extracorporeal shock wave therapy, ultrasound-guided percutaneous lavage, corticosteroid injection and combined treatment for rotator cuff calcific tendinopathy: a network meta-analysis of RCTs. Eur J Orthop Surg Traumatol. 27(3):381–390. PMID: 27554465. DOI: 10.1007/s00590-016-1839-y

  6. Moseley HF, Goldie I (1963). The arterial pattern of the rotator cuff of the shoulder. J Bone Joint Surg Br. 45-B(4):780–789. (Vascular anatomy β€” critical zone)