Abstract
Rationale:
Although the totally implantable venous access ports have been widely used for chemotherapy and parenteral nutrition because of their safety and durability, some postoperative complications may still occur, such as catheter fracture, which can occur so silently and be discovered after several cycles of chemotherapy.
Patient concerns:
A 55-year-old male received the implantation of a chest wall venous port via the right internal jugular vein approach in an external hospital more than 3 years ago due to the need for chemotherapy for pancreatic cancer. On the 1221st catheter day, blood return could not be aspirated.
Diagnoses:
A chest X-ray confirmed the catheter rupture.
Interventions:
An emergency endovascular surgery was performed to remove the ruptured catheter and the port body, and a new venous port was implanted.
Outcomes:
Upon careful review of the medical history, the patient could not feel the cord-like structure in front of the right clavicle 3 months ago. Since the previous chemotherapy sessions had gone smoothly, the patient did not pay much attention to it. This also implies that the catheter rupture might have occurred at that time. Moreover, several chemotherapy infusions were still carried out after the catheter rupture, and the patient did not experience any discomfort.
Lessons:
The catheter rupture of venous ports can present silently, meaning the port can still be used for smooth infusion without any patient’s discomfort, which precisely delays the diagnosis, and may lead to life-threatening complications such as pulmonary embolism. Standardized maintenance of the venous port, regular chest imaging examinations, and careful interpretation of the imaging findings are helpful for the early diagnosis of such silent catheter ruptures.
Keywords: catheter fracture, endovascular intervention, silent, TIVAP
1. Introduction
Since 1982, the totally implantable venous access ports (TIVAPs) have revolutionized the long-term venous access management for chemotherapy administration and total parenteral nutrition in oncology patients. This implantable device has demonstrated clinical reliability, operational safety, and extended service longevity, thereby substantially enhancing patient comfort and quality of life metrics in cancer care settings.[1] Despite demonstrating a lower overall incidence of complications than the peripherally inserted central catheters, TIVAP-related adverse events persist within a clinically significant range of 1.8% to 14.4% in contemporary studies.[2] Of particular clinical concern, catheter fracture represents a critical device failure event, with reported incidence rates ranging from 0.1% to 2.1% in contemporary case series.[3,4] The incidence of catheter rupture was 1.8% in the internal jugular vein (IJV) and in the subclavian vein 1.1% to 5.0%.[5] Although the rate is low, the catheter fracture can be fatal if the broken catheter migrates to the heart and causes arrhythmia or pulmonary embolism, respectively. Clinically, catheter integrity compromise manifests through loss of blood reflux, post-infusion infusate extravasation, port-site edema, and localized tenderness, which help in an early diagnosis of catheter fracture.
However, cases in which the time of catheter rupture is discovered a long time after it occurs are rarely reported. Herein, we will report such an uncommon but alarming case, in which therapeutic infusions were successfully maintained for months post-catheter fracture without treatment interruption.
2. Case presentation
A 55-year-old male presented with pancreatic adenocarcinoma confirmed by core needle biopsy 3 years ago. Then a TIVAP implantation (Bard Access Systems, Inc., Salt Lake City) via the IJV was successfully performed, followed by initiation of neoadjuvant chemotherapy (albumin-bound paclitaxel 200 mg/m2 + gemcitabine 1650 mg/m2) on day 1 and 8 of a 21-day cycle. Subsequently, the patient underwent pancreatoduodenectomy with portal vein reconstruction after 3 months, achieving uneventful postoperative recovery. Adjuvant chemotherapy (gemcitabine 1600 mg/m2 on days 1 and 8 + capecitabine 1500 mg/m2/day on days 1–14) was administered every 21 days in the following 6 months.
Six months ago, surveillance showed a sharp increase in CA19-9 levels, rising from 16.64 to 5744.7 U/mL. A subsequent positron emission tomography-computed tomography scan revealed soft tissue densities in the retroperitoneal region, indicating metastatic progression. Consequently, a modified AG regimen of gemcitabine (1600 mg/m2) and albumin-bound paclitaxel (200 mg/m2) was started on days 1 and 15 of a 28-day cycle.
On the 1221st catheter day, during routine catheter maintenance procedures, approximately 2 mL of dark-brown-colored blood was aspirated from the venous port. Clinical assessment revealed a concave deformation in the subcutaneous catheter tract region (Fig. 1A). Concurrently, visual inspection of the aspirated specimen revealed opalescent fluid with visible sedimentations. Following clinical notification of suspected port dysfunction, a chest radiograph was performed and a catheter fracture was observed (Fig. 1B) with the fractured catheter coiled within the superior vena cava (SVC) (Fig. 1C). The plan for the endovascular removal of the free ruptured catheter was promptly initiated 45 minutes after the diagnosis.
Figure 1.
(A) The subcutaneous tunnel in front of the collarbone collapsed. (B) The frontal chest radiograph indicated that the catheter and the port body were disconnected. (C) The lateral chest radiograph showed that the broken catheter was approximately located in the SVC. (D) The catheter was removed by the snare device. (E) The isolated port body with a remaining part of the catheter; (F) The broken catheter and the isolated port body. SVC = superior vena cava.
Following successful percutaneous access to the right common femoral vein, a guidewire-catheter coaxial technique was used to advance the catheter into the SVC for angiography. No peri-catheter thrombus was observed in the SVC (see Video S1, which demonstrates no catheter-associated venous thrombosis). The snare device was used for catheter extraction (see Video S2, which demonstrates an intravascular snare was used to capture one end of the catheter), and the retrieval of the free-floating catheter was ultimately accomplished through the established femoral access sheath (Fig. 1D) (see Video S3, which demonstrates the removal of the catheter from the sheath).
Utilizing the previous incision over the port pocket, the tissues were dissected in layers until the port reservoir was completely explanted. The catheter fractured at the luer lock connection (Fig. 1E) and the retrieved catheter tip demonstrated a 22.5-cm length matching original implantation records (Fig. 1F). The residual catheter tunnel orifice was systematically closed. Subsequently, the ultrasound-guided cannulation of the right axillary vein was performed, and a new venous port (ZS2 Series Implantable Drug Delivery Device; ZS2-II-1.8/1.2-750; Beijing Yue tong Medical Equipment Co., Ltd., Suzhou, Jiangsu, China) was implanted inside the original port pocket using the surgical technique method described previously.[6] The total implanted catheter length was measured at 21.5 cm, with radiographic confirmation of the catheter tip positioning at the seventh thoracic vertebral body level. The incision was closed utilizing a subcuticular suture technique, followed by a subsequent standardized hemostatic compression applied at the right common femoral venous access site. During the approximately 4-month follow-up monitoring after the surgery, the patient demonstrated satisfactory wound epithelization and completed 4 chemotherapy cycles without any catheter-associated complications.
To investigate the causes of the condition, a retrospective analysis of the patient’s medical history was conducted. The patient reported that around 3 months ago, the subcutaneous catheter tract in the cervico-clavicular region suddenly disappeared, indicating a possible catheter rupture. However, this change was not reported to the clinical team due to the lack of symptoms like pain or dyspnea. Prior institutional records indicated that the venous port system was intact on CT on the 1107th catheter day (see Video S4, which demonstrates that the catheter and port body were well connected), but a fracture was noted by the 1193rd day (see Video S5, which demonstrates the disconnection of the catheter and port body). This critical finding was not documented in the clinical records. During the 16-week chemotherapy regimen, temporary catheter issues arose during routine port maintenance. However, after the nurse instructed the patient to move his neck and shoulder and cough, blood recovery improved significantly. Continuous cardiorespiratory monitoring confirmed the absence of acute distress, allowing for the seamless administration of cytotoxic therapy. This case exemplifies a striking and rare phenomenon: the successful delivery of chemotherapy through a fractured implantable venous port for 3 months.
3. Discussion and conclusions
Infusion port catheter fracture represents a rare late-phase complication. The interval between implantation and discovery of catheter fracture was 451.6 ± 325.4 days.[7] To gain further insight into the clinical management of port catheter fracture, we reviewed a large number of literature between 1988 and 2024 and summarized their clinical characteristics (Tables 1 and 2). The most common fracture site of the catheter is the port catheter junction, with an incidence of about 83%.[8] This observation aligns with our case study findings. A slight male predominance in adult cohorts was shown. Most patients with catheter ruptures showed mild symptoms, like chest or back pain, catheter dysfunction, and typically could not use the catheter afterward. Notably, 41% of patients exhibit no immediate symptoms, and the catheter fracture was identified by imaging examinations, which manifested as silence.
Table 1.
The brief review of literature related to catheter fracture of implantable venous port (basic information).
| No. | Year | Author | Article type | Number of case | Pocket position | Tunnel | Gender | Age (yr) | Manufacturer; specification |
|---|---|---|---|---|---|---|---|---|---|
| 1 | 1988 | Thomas et al | Case | 1 | Chest wall | N/A | M | 24 | N/A |
| 2 | 1991 | Dr Rene, Lafreniere | Case | 1 | N/A | N/A | F | 35 | Port-A-Cath; 2.8 mm |
| 3 | 1992 | Inoue et al | Case | 1 | Chest wall | Yes | M | 45 | Infuse-A-Port; 2.5 mm |
| 4 | 1993 | Röggla et al | Case | 1 | N/A | N/A | M | 36 | Port-a-Cath; N/A |
| 5 | 1998 | Nostdahl et al | Case | 3 | Chest wall | Yes | F, F, M | 30, 69, and 42 | Braun; N/A |
| 6 | 1998 | Vadlamani et al | Case | 3 | N/A | N/A | M, F, F | 24, 31, and 41 | Case 1: Pharmacia NuTech; Cases 2–3: N/A |
| 7 | 1998 | Biffi et al | Retrospective cohort study | 5 | N/A | N/A | N/A | N/A | Bard; 8 F |
| 8 | 2000 | Khanna et al | Case | 1 | Chest wall | N/A | M | 70 | Port-A-Cath; N/A |
| 9 | 2003 | Schummer et al | Case | 2 | Chest wall | N/A | F | 61 and 40 | N/A |
| 10 | 2003 | Bessoud et al | Retrospective cohort study | 100 | N/A | N/A | N/A | 3 mo to 75 yr | N/A |
| 11 | 2004 | Filippou et al | Case | 4 | Chest wall | N/A | F | 65, 68, 74, and 56 | Port-A-Cath; N/A |
| 12 | 2004 | Yildizeli et al | Retrospective cohort study | 4 | Chest wall | Yes | N/A | N/A | N/A |
| 13 | 2004 | Gowda et al | Case | 1 | Yes | N/A | F | 34 | N/A |
| 14 | 2005 | Hackert et al | Case | 1 | Chest wall | No | F | 49 | Fresenius; N/A |
| 15 | 2005 | Kapadia et al | Case | 1 | Chest wall | Yes | F | 16 | HDC Corporation; N/A |
| 16 | 2006 | Kim et al | Case | 1 | Chest wall | N/A | F | 39 | Braun; 8.5 F |
| 17 | 2006 | Dillon et al | Retrospective cohort study | 4 | Chest wall | N/A | N/A | Average 11.8 | Bard; 6.6 F |
| 18 | 2006 | Surov et al | Retrospective cohort study | 11 | Chest wall | N/A | F: 3, M: 8 | Average 53 | Fresenius Kabi GmbH, Baxter, Germany, pfm AG; N/A |
| 19 | 2009 | Seck et al | Case | 3 | Forearm, | N/A | F | 84: case 2; N/A: cases 1 and 3 | N/A |
| 20 | 2009 | Cheng et al | Retrospective cohort study | 92 | N/A | N/A | M: 47, F: 45 | 53.8 ± 13.5 | Bard, Arrow International, Deltec; N/A |
| 21 | 2010 | Karaman et al | Retrospective cohort study | 2 | Chest wall | Yes | N/A | N/A | Braun; N/A |
| 22 | 2011 | Subramaniam et al | Retrospective cohort study | 9 | Chest wall | N/A | F | N/A | Bard; 7 F or 8 F |
| 23 | 2011 | Wu et al | Retrospective cohort study | 59 | N/A | N/A | M: 21; F: 38 | 54.32 ± 13.11 | Arrow International Fr. 8.1: 51 cases, Bard Fr. 8: 5 cases, Bard Fr. 6.6: 3 cases |
| 24 | 2012 | Busch et al | Retrospective cohort study | 6 | Uparm | Yes | M: 5 cases; N/A: 1 case |
70 and 57: 2 cases; N/A: 4 cases | Cook; 5.0/6.5 F |
| 25 | 2012 | Schenck et al | Retrospective cohort study | 1 | Chest wall | No | N/A | N/A | FA PHS Medical; N/A |
| 26 | 2012 | Kim et al | Retrospective cohort study | 1 | Chest wall | N/A | N/A | N/A | N/A |
| 27 | 2013 | Burbridge et al | Retrospective cohort study | 11 | Arm | Yes | M: 2, F: 9 | Average 54.5 | Cook Canada; 5 F |
| 28 | 2014 | Pignataro et al | Case | 1 | Chest wall | N/A | M | 41 | Bard; 8 F |
| 29 | 2014 | Balsorano et al | Retrospective cohort study | 12 | Chest wall | N/A | F: 7; M: 5 | 59.3 ± 11.1 | Bard; N/A |
| 30 | 2014 | Nagasawa et al | Retrospective cohort study | 4 | N/A | N/A | N/A | N/A | BMedicon; N/A |
| 31 | 2015 | Tazzioli et al | Case | 1 | Chest wall | N/A | F | 50 | Bard; 8 F |
| 32 | 2015 | Ghaderian et al | Case | 1 | N/A | N/A | F | 8 | N/A |
| 33 | 2016 | Ko et al | Case | 1 | Chest wall | Yes | F | 50 | DistricAth; 9 F |
| 34 | 2016 | Kojima et al | Retrospective cohort study | 16 | Chest wall | Yes | N/A | N/A | Bard; 8 F |
| 35 | 2016 | Mery et al | Case | 1 | Chest wall | N/A | F | 52 | N/A |
| 36 | 2017 | Fujimoto et al | Case | 1 | Chest wall | N/A | F | 61 | N/A |
| 37 | 2018 | Barton et al | Retrospective cohort study | 1 | N/A | N/A | M | N/A | N/A |
| 38 | 2018 | Garcez et al | Case | 1 | Chest wall | N/A | F | 57 | N/A |
| 39 | 2018 | Wu et al | Retrospective cohort study | 17 | N/A | N/A | M: 13 cases, F: 4 cases | Average 48 | N/A |
| 40 | 2019 | Lukito et al | Case | 1 | N/A | N/A | F | 33 | N/A |
| 41 | 2019 | Sun et al | Retrospective cohort study | 1 | Chest wall | Yes | N/A | N/A | Bard; 6 F |
| 42 | 2019 | Saijo et al | Case | 3 | Chest wall | Yes | M, F, F | 64, 78, and 59 | Bard; N/A |
| 43 | 2021 | Chuah et al | Case | 1 | Chest wall | Yes | M | 50 | N/A |
| 44 | 2021 | Sudhakar et al | Case | 1 | Chest wall | N/A | F | 60 | N/A |
| 45 | 2021 | Chen et al | Case | 1 | Chest wall | N/A | F | 43 | N/A |
| 46 | 2022 | Shah et al | Case | 1 | N/A | N/A | F | 51 | N/A |
| 47 | 2022 | Azeemuddin et al | Case | 1 | Chest wall | N/A | F | 67 | N/A |
| 48 | 2022 | Li et al | Retrospective cohort study | 31 | Chest wall | Yes | N/A | N/A | N/A |
| 49 | 2022 | Goyal et al | Case | 1 | N/A | N/A | F | 3 | N/A |
| 50 | 2023 | Takahashi et al | Case | 1 | Chest wall | Yes | M | 83 | Bard; 8.0 F |
| 51 | 2023 | Abbasov et al | Case | 1 | Chest wall | N/A | F | 53 | N/A |
| 52 | 2023 | Matta et al | Case | 1 | Chest wall | N/A | M | 85 | N/A |
| 53 | 2024 | Kordykiewicz et al | Case | 1 | Chest wall | Yes | M | 67 | Braun; N/A |
| 54 | 2024 | Dave et al | Case | 1 | Chest wall | Yes | F | 56 | N/A |
F = female, M = male, N/A = not mentioned in literature.
Table 2.
The brief review of literature related to catheter fracture of implantable venous port (catheter fracture information).
| No. | Year | Author | Venous approach | Time of fracture discovery | Position of the free catheter | Fracture site | Patient symptoms at the time of rupture | Continous infusion through the port | Reasons for catheter breakage | Treatment for broken catheter | Treatment for portal |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | 1988 | Thomas et al | SCV | 13 mo | Right atrium, right ventricle | Between the first rib and collarbone | Pain; no blood return | No | Shear force resulting from movement of the shoulder and pectoralis major | Endovascular removal | Surgical removal |
| 2 | 1991 | Dr Rene, Lafreniere | Right SCV | 11 mo | Right atrium | Between the first rib and collarbone | Infusion pain | No | Pinch-off syndrome | Endovascular removal | N/A |
| 3 | 1992 | Inoue et al | Left SCV | 19 mo | Just catheter crack | Between the first rib and collarbone | Pain, dysfunction | No | Pinch-off syndrome | Surgical removal | Surgical removal |
| 4 | 1993 | Röggla et al | Left SCV | 12 mo | Pulmonary artery | Venous entrance | Chest X-rays | N/A | Pinch-off syndrome | Endovascular removal | Surgical removal |
| 5 | 1998 | Nostdahl et al | SCV | 5–6 wk, 7 mo, 1 mo | Just catheter crack | Between the first rib and collarbone | Tenderness, Pain during infusion, Difficulty in drawing blood; Low infusion speed, Redness of the skin; | No | Pinch-off syndrome | Surgical removal | Surgical removal |
| 6 | 1998 | Vadlamani et al | N/A | Case 1: 4 mo; Case 2: N/A; Case 3: 4 wk |
Case 1: Pulmonary artery; Case 2: Right atrium; Case 3: N/A |
N/A | Case 1: No return of blood; Case 2: Chest X-rays; Case 3: Dysfunction |
No | N/A | Cases 1–2: Endovascular removal | N/A |
| 7 | 1998 | Biffi et al | SCV, Cephalic vein | 66 ± 18 d in 2 cases; 10 mo in another case; | N/A | N/A | Palpitations and Chest discomfort in 2 cases; Asymptomatic in the other 3 cases |
N/A | Pinch-off syndrome for 1 case | Endovascular removal | N/A |
| 8 | 2000 | Khanna et al | Right SCV | 31 wk | Right atrium | Between the first rib and collarbone | Right shoulder pain | No | Pinch-off syndrome | Endovascular removal | N/A |
| 9 | 2003 | Schummer et al | Right SCV | 1 wk after chemotherapy ends; 12 mo | Right ventricle; left pulmonary artery | Middle segment | Difficult injection | No | N/A | Endovascular removal | Surgical removal |
| 10 | 2003 | Bessoud et al | SCV 、IJV | 290 ± 200 d | pulmonary artery: 26, right ventricle: 24, right atrium: 23, IVC: 7, SVC: 17, hepatic vein: 2, thymic vein: 1 | N/A | Resistance in the injection and No blood return. | No | Accidental sectioning during retrieval: 7, Loss during implantation: 3, N/A-90 |
Endovascular removal: 95, not retrieved: 5. | N/A |
| 11 | 2004 | Filippou et al | SCV | 6, 18, 14, 8, and mo | 1. Right atrium 2. Right ventricle 3. Right atrium 4. Partial segment remained in subcutaneous tissue | N/A | Back pain: 1, Infusion resistance: 3 | No | Reduced elasticity of the catheter and Wrong manipulations | Thoracotomy: 1-failed and receiving anticoagulant therapy; Endovascular removal: 3 | Surgical removal |
| 12 | 2004 | Yildizeli et al | N/A | 126, 140, 154, and 175 d | 3 in SVC and 1 in pulmonary artery | N/A | Asymptomatic, Impaired return of blood and detected by a routine chest X-ray | No | Pinch-off syndrome | Endovascular removal | N/A |
| 13 | 2004 | Gowda et al | Right SCV | 3 yr | Right ventricle | Between the first rib and collarbone | Shortness of breath, palpitations, ventricular tachycardia | No | Pinch-off syndrome | Endovascular removal | Surgical removal |
| 14 | 2005 | Hackert et al | Cephalic vein | 2 yr | Right upper lobe of the lung | N/A | Intermittent coughing, Shortness of breath, General weakness, Failing blood aspiration | No | N/A | Thoracotomy | Remain |
| 15 | 2005 | Kapadia et al | Right SCV | 24 mo | Istal catheter embedded into the myocardium of the right ventricle, whereas the proximal end was stuck to the wall of the SVC. |
Catheter to port connection | Asymptomatic | No | Irregular maintenance | Endovascular removal failed, and it was removed by thoracotomy | Surgical removal |
| 16 | 2006 | Kim et al | SCV | 3 mo | Pulmonary artery | Between the first rib and collarbone | Chest and chin pain | No | Pinch-off syndrome | Endovascular removal | N/A |
| 17 | 2006 | Dillon et al | N/A | Average 1075 d | Pulmonary artery or heart | Catheter to port connection: 3 cases, proximal to the clavicle: 1 case |
Pain or Resistance to Infusion | No | Excessive pressure at the connection between the catheter and the port, conventional wear | Endovascular removal | N/A |
| 18 | 2006 | Surov et al | SCV | Average 203 d | Pulmonary artery | Between the first rib and collarbone in 9 cases; Catheter to port connection in 2 cases |
Catheter dysfunction in 7 cases; asymptomatic in 4 cases | No | Pinch-off syndrome iin 9 cases; incorrect locking of the steel ring or flaws in the system itself in 2 cases | Endovascular removal | N/A |
| 19 | 2009 | Seck et al | Vena brachialis-case 2; N/A-cases 1 and 3 | N/A | Pulmonary artery: cases 1 and 2; dislocation of the connection: case 3 |
1. Proximal catheter; 2. N/A; 3. Catheter to port connection |
Infusion resistance; Weakness, Dizziness, Breathing difficulties, No return of blood | No | Problems with the material. | N/A | Surgical removal |
| 20 | 2009 | Cheng et al | SCV | 451.6 ± 325.4 | Right atrium, IVC, SVC | Catheter to port connection: 77 cases; proximal part: 12 cases; Distal portion: 3 cases |
Resistance during infusion: 51; Asymptomatic: 33; The rest unspecified |
No | Faulty connection and alignment; Unskillful operator, forceful port irrigation and lower rate of cut-down approach | Endovascular removal in 90 cases; endovascular removal failed in 2 cases; | N/A |
| 21 | 2010 | Karaman et al | IJV | Second and third day | Just catheter crack | Venous entrance | Swelling and pain in the neck | No | Forceful saline infusion | Surgical removal | Surgical removal |
| 22 | 2011 | Subramaniam et al | SCV | Average 197 d | Right ventricle: 4 cases, Pulmonary artery: 3 cases |
N/A | Asymptomatic-most | No | The design and manufacturing deficiencies of this catheter | Endovascular removal | N/A |
| 23 | 2011 | Wu et al | Right SCV: 26 cases, left SCV: 3 cases, right IJV: 1 case, right cephalic vein: 22 cases, left cephalic vein: 7 cases |
496.03 ± 321.41 | No dislodged catheter: 7 cases, Right atrium: 19 cases, IVC: 20 cases, Right ventricle: 12 cases, Pulmonary artery: 1 case |
Lock nut area: 52 cases; Proximal end of catheter: 3 cases, Perforation only: 4 cases |
Catheter dysfunction: 9; Asymptomatic: 49; Infection: 1 case |
No | Port type Arrow Fr. 8.1, female gender, and implantation of the intravenous port via the subclavian route | Endovascular removal: 58 cases; catheter shortening: 1 case | N/A |
| 24 | 2012 | Busch et al | Brachial vein | N/A | Pulmonary artery: 2 cases; Just catheter crack: 4 cases |
N/A: 2 cases, Proximal leakage: 4 cases |
Pain, Swelling and Contrast agent extravasation: 4; Chest X-rays: 2 |
No | Excessive shoulder movement: 2; N/A: 4 | Endovascular removal | Surgical removal |
| 25 | 2012 | Schenck et al | Cephalic vein | N/A | Pulmonary artery | N/A | N/A | N/A | N/A | N/A | N/A |
| 26 | 2012 | Kim et al | SCV | 6 mo | Right atrium | Between the first rib and collarbone | Palpitations and Chest tightness | No | Pinch-off syndrome | Endovascular removal | N/A |
| 27 | 2013 | Burbridge et al | N/A | Average 682 d | 3 in peripheral venous system; 8 in pulmonary artery |
Venous entrance | Chest X-rays | N/A | Arm movement or narrow and fibrotic veins | Endovascular removal | N/A |
| 28 | 2014 | Pignataro et al | Right IJV | 24 mo | Right atrium, within the coronary sinus | Middle segment | Neck pain and Swelling during infusion | No | N/A | Endovascular removal | N/A |
| 29 | 2014 | Balsorano et al | IJV | 589–1842 d | N/A | N/A | Catheter blockage: 3; Drug extravasation: 2; Asymptomatic: 7 |
N/A: 7; No: 5 | “Out-of-plane” approach and type of port | N/A | N/A |
| 30 | 2014 | Nagasawa et al | IJV: 3 cases; SCV: 1 case | N/A | N/A | N/A | N/A | N/A | Chronic stress in IJV approach; Pinch-off syndrome in SCV approach | N/A | N/A |
| 31 | 2015 | Tazzioli et al | Right IJV | 35 mo | Right ventricle | The proximal third | Catheter dysfunction | No | N/A | Endovascular removal failed and follow-up | N/A |
| 32 | 2015 | Ghaderian et al | N/A | 3 yr | Right atrium | N/A | Asymptomatic | No | N/A | Endovascular removal | Surgical removal |
| 33 | 2016 | Ko et al | Right IJV | 3 mo after final chemotherapy | Right atrium | Catheter to port connection | Swelling of the right neck | No | Irregular maintenance | Endovascular removal | Surgical removal |
| 34 | 2016 | Kojima et al | Right IJV | Average 621 d | Right chamber of the heart, pulmonary artery, or coronary sinus | Venous entrance: 14 cases; Proximal catheter: 2 cases |
Subcutaneous swelling, Skin reddening and/or Pain at the port or along the subcutaneous Catheter tract: 12 cases; Asymptomatic: 4 cases |
No | Weaknesses of catheter material, pressure-sensitive valve design, bending stress concentration at the venous entrance, excessive depth at the catheter tip position, low body mass index, age and mobility, indwelling time. | Endovascular removal: 8 cases, left the catheter in coronary sinus: 1 case | Surgical removal |
| 35 | 2016 | Mery et al | Left SCV | 9 mo | The great saphenous vein on the medial side of the right knee | Between the first rib and collarbone | Coughing, Infusion resistance | No | Pinch-off syndrome | Surgical removal | Surgical removal |
| 36 | 2017 | Fujimoto et al | Right SCV | 63 mo | Pulmonary artery | Proximal catheter | Infusion resistance | No | Thrombotic occlusion | Endovascular removal | Surgical removal |
| 37 | 2018 | Barton et al | N/A | 26 mo | N/A | N/A | N/A | N/A | N/A | N/A | Surgical removal |
| 38 | 2018 | Garcez et al | SCV | 26 mo | IVC | Between the first rib and collarbone | Asymptomatic | N/A | Pinch-off syndrome | Endovascular removal | Surgical removal |
| 39 | 2018 | Wu et al | SCV | 2 h to 53 mo | SVC, IVC, right atrial brachial vein, right ventricle, pulmonary artery | Middle segment, Distal 2/3: 13 cases | Asymptomatic-Most, Chest discomfort or Palpitations-a few | N/A | Pinch-off syndrome: 13 cases, the rest unspecified. | Endovascular removal | Surgical removal |
| 40 | 2019 | Lukito et al | N/A | 1 yr | Coronary sinus | N/A | Asymptomatic | No | N/A | Endovascular removal failed and the patient refused thoracotomy | Surgical removal |
| 41 | 2019 | Sun et al | Right IJV | N/A | N/A | N/A | N/A | N/A | N/A | N/A | N/A |
| 42 | 2019 | Saijo et al | IJV | 21, 31, and 38 mo | Right atrium, IVC, right ventricle | Middle segment | Chest X-ray in case 1, Catheter dysfunction in cases 2–3 | No | 1. Long-term repeated stretching force 2. Groshong silicone tube material is fragile |
Endovascular removal | Surgical removal |
| 43 | 2021 | Chuah et al | SCV | 4 yr | Right ventricle | Between the first rib and collarbone | Occasional palpitations and chest discomfort | No | Pinch-off syndrome | Endovascular removal | Surgical removal |
| 44 | 2021 | Sudhakar et al | SCV | 14 mo | Coronary sinus, right ventricle | Between the first rib and collarbone | Asymptomatic | N/A | Pinch-off syndrome | Endovascular removal | Surgical removal |
| 45 | 2021 | Chen et al | Right IJV | 163 d | Pulmonary artery | N/A | Wheezing, Coughing, Chest tightness, Shortness of breath, Difficulty breathing after exercise | No | N/A | Endovascular removal | N/A |
| 46 | 2022 | Shah et al | N/A | N/A | Right atrium, Right ventricle | Middle segment | Infusion resistance | No | N/A | Endovascular removal | N/A |
| 47 | 2022 | Azeemuddin et al | N/A | 24 mo | Right atrium | Proximal catheter | No blood return; drowsiness; Loss of appetite | No | N/A | Endovascular removal | Surgical removal |
| 48 | 2022 | Li et al | SCV | N/A | N/A | Proximal end of the catheter: 17 cases; Between the first rib and collarbone: 14 cases |
N/A | N/A | Clamping syndrome: 14; Separation of infusion port from the proximal catheter: 17 |
Endovascular removal | Surgical removal |
| 49 | 2022 | Goyal et al | N/A | 25 d | Right ventricle, pulmonary artery | N/A | Severe chest pain and fever | No | N/A | Thoracotomy | N/A |
| 50 | 2023 | Takahashi et al | Right IJV | 96 mo | Coronary sinus | Middle segment | Ventricular fibrillation | No | N/A | Thoracotomy | Surgical removal |
| 51 | 2023 | Abbasov et al | Right SCV | 36 mo | Pulmonary artery | N/A | N/A | No | Pinch-off syndrome | Remain | Surgical removal |
| 52 | 2023 | Matta et al | Right SCV | 36 d | Right ventricle | Between the first rib and collarbone | No blood return | No | Pinch-off syndrome | Endovascular removal | Surgical removal |
| 53 | 2024 | Kordykiewicz et al | N/A | 1 mo | Pulmonary artery | N/A | Persistent cough, Weakness, Nausea and Heartburn | No | N/A | Thoracotomy | Surgical removal |
| 54 | 2024 | Dave et al | Right IJV | N/A | Right ventricle, pulmonary artery | N/A | Catheter dysfunction | No | N/A | Endovascular removal | N/A |
IJV = internal jugular vein, IVC = inferior vena cava, N/A = not mentioned in literature, SCV = subclavian vein, SVC = superior vena cava.
This case is unique as the infusion port catheter was fractured, yet normal infusions continued for 3 months. Unlike most reports where issues arise immediately after fracture, this suggests that assessing catheter rupture should not rely solely on symptoms or routine exams but also consider individual circumstances. This case offers some new perspectives on catheter rupture management in infusion ports, enhancing our understanding and aiding in the improvement of clinical strategies.
Fracture of an implantable port catheter may have several causes, except for the pinch-off syndrome associated with the subclavian vein approach. Previous studies have demonstrated that catheter breakage is associated with multiple factors. On one hand, it correlates with patients’ occupation, low body mass index, age, lifestyle habits, and mobility, as well as prolonged indwelling time. On the other hand, excessive depth of the catheter tip position, material weaknesses, design and manufacturing deficiencies of the catheter, and bending stress concentration at the venous entrance also contribute to catheter failure. However, in recent years, advancements in material science, technological improvements, and enhanced management practices have significantly reduced the incidence of catheter breakage in infusion ports. This patient’s job involved repetitive arm movements for 4 months before the catheter rupture, likely contributing to mechanical stress and material fatigue in the catheter wall, which may lead to its failure. Flushing a catheter with a small syringe can create excessive pressure, weakening it and increasing the risk of breakage. Additionally, the materials used and repeated tensile stress can further deteriorate the catheter’s strength, leading to fractures.[9–11] A catheter fracture at the port catheter junction can result from external compression and material fatigue due to repeated bending from shoulder movement. The port implantation method and the distance from the clavicle also increase the risk of fracture, as sharp angles can create higher local pressure, leading to fatigue cracks.[12] In the retrospective study by Matsunari et al, venipuncture performed within 3 cm of the clavicle combined with maintaining a gentle catheter curvature (approximately 90°) was associated with reduced catheter fracture risk.[13]
In this patient, chemotherapy administration over 3 months occurred without adverse reactions, such as drug extravasation or phlebitis, despite a catheter fracture. This unusual situation may be due to an inflammatory response, fibroblasts, and granulation tissue around the catheter, creating a false passage between the port and the IJV. When poor blood aspiration occurs, changing body position or coughing can increase thoracic pressure, pumping blood from the IJV into the port so that blood can still be aspirated. The fibrotic tunnel wall may prevent drug penetration and diffusion, allowing the patient to avoid significant pain or discomfort. From another bold perspective, it is also worth considering whether, by simply removing the fractured catheter, the port can be continuously used for infusion until the end of chemotherapy. Of course, this requires verification with a large amount of data and ethical considerations.
The patient continued chemotherapy despite a catheter fracture but did not develop complications like phlebitis or pulmonary embolism. This case is interesting, and the result is fortunate for the patient, yet alarming for doctors. It offers valuable lessons and suggests areas for improvement in medical practice. The 2024 Infusion Nurses Society guidelines recommend an annual chest X-ray assessment of port position and integrity. If blood return is poor during port use, have the patient change positions (e.g., raise their arm or take deep breaths).[12] This alters thoracic pressure or vessel shape, helping the catheter tip disengage from the vessel wall. Reviewing prior port maintenance, nurses may have performed improper blood aspiration. Before infusion, discard 2 to 3 mL of venous blood. However, nurses may not always collect enough to identify port issues. If there is poor blood return from the TIVAP, an X-ray should be considered to check for catheter fractures.[14] Patient education after venous port implantation is vital. It should cover port types, complication recognition, and daily activity precautions. Strong cannulation skills and prompt medical treatment can help prevent port catheter fractures and serious complications.[15]
To summarize, catheter fracture of TIVAPs may manifest as clinically silent device failure without overt perivascular chemotherapeutic extravasation. This asymptomatic catheter disruption underscores the critical necessity for full patient education, standardized maintenance of the infusion port, and timely imaging examination, which are crucial. They help detect and intervene early, thus preventing serious complications.
Author contributions
Conceptualization: Linlin Xiang, Jingjin Wu.
Data curation: Haoping Chen, Linlin Xiang.
Methodology: Jingjin Wu.
Supervision: Jingjin Wu.
Validation: Jingjin Wu.
Visualization: Haoping Chen, Linlin Xiang.
Writing – original draft: Haoping Chen, Linlin Xiang.
Writing – review & editing: Jingjin Wu.
Abbreviations:
- IJV
- internal jugular vein
- SVC
- superior vena cava
- TIVAP
- totally implantable venous access port
Informed consent has been obtained from the patient.
This study was approved by the Ethics Committee of the Fourth Affiliated Hospital Zhejiang University School of Medicine (K2025044).
The authors have no funding and conflicts of interest to disclose.
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
How to cite this article: Xiang L, Chen H, Wu J. Silent port catheter fracture with normal infusion: A case report and literature review. Medicine 2025;104:40(e45004).
Contributor Information
Linlin Xiang, Email: xll812@zju.edu.cn.
Haoping Chen, Email: 8019101@zju.edu.cn.
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