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Comparison of complication types in patients receiving vesicant intravenous antimicrobials or vasopressors via midlines and peripherally inserted central catheters

Published online by Cambridge University Press:  05 September 2024

Bryan Grigg ,
Nishant Varghese ,
Christi Knapp ,
Sabra L. Shay ,
Geraldine Jones ,
James P. Herlihy Open the ORCID record for James P. Herlihy [Opens in a new window] ,
Prasad Manian ,
Bradley Lembcke  and
Mayar Al Mohajer Open the ORCID record for Mayar Al Mohajer [Opens in a new window]
Bryan Grigg
Affiliation:
Baylor College of Medicine, School of Medicine, Houston, TX, USA
Nishant Varghese
Affiliation:
Baylor St. Luke’s Medical Center, Houston, TX, USA
Christi Knapp
Affiliation:
Baylor St. Luke’s Medical Center, Houston, TX, USA
Sabra L. Shay
Affiliation:
Department of Clinical Intelligence, Premier Inc., Charlotte, NC, USA
Geraldine Jones
Affiliation:
Baylor St. Luke’s Medical Center, Houston, TX, USA
James P. Herlihy
Affiliation:
Department of Medicine, Section of Pulmonary and Critical Care, Baylor College of Medicine, Houston, TX, USA
Prasad Manian
Affiliation:
Department of Medicine, Section of Pulmonary and Critical Care, Baylor College of Medicine, Houston, TX, USA
Bradley Lembcke
Affiliation:
Baylor St. Luke’s Medical Center, Houston, TX, USA
Mayar Al Mohajer*
Affiliation:
Baylor St. Luke’s Medical Center, Houston, TX, USA Department of Medicine, Section of Infectious Diseases, Baylor College of Medicine, Houston, TX, USA
*
Corresponding author: Mayar Al Mohajer; Email: Mohajer@bcm.edu

Abstract

We assessed adverse events in hospitalized patients receiving selected vesicant antibiotics or vasopressors administered through midline catheters or peripherally inserted central catheters (PICC). The rates of catheter-related bloodstream infections, thrombosis, and overall events were similar across the two groups, while occlusion was higher in the PICC group.

Information

Type
Concise Communication
Information
Antimicrobial Stewardship & Healthcare Epidemiology , Volume 4 , Issue 1 , 2024 , e116
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Introduction

Peripherally inserted central catheters (PICC) are frequently used to obtain durable intravenous access due to their ease of insertion, relative safety, and facilitation of outpatient parenteral antimicrobial therapy. However, in hospitalized patients, PICC have a similar risk of catheter-related bloodstream infections (CRBSI) as central venous catheters (CVC). Reference Turcotte, Dubé and Beauchamp1,Reference Chopra, O’Horo, Rogers, Maki and Safdar2 Midline catheters (MC) have emerged as a safer alternative and are associated with reduced rates of CRBSI compared to PICC but may convey an increased risk of thrombosis. Reference Urtecho, Torres Roldan and Nayfeh3,Reference Swaminathan, Flanders, Horowitz, Zhang, O’Malley and Chopra4

A key component when choosing line type is the drug to be administered. Until the last decade, vesicant drugs such as vasopressors and antibiotics have been limited to administration via central catheters. Consequently, the effect of vesicant drugs on adverse events in MC is unknown. Reference Gorski, Hadaway and Hagle5–Reference Gershengorn, Basu and Horowitz9 Thus, we aimed to compare rates of CRBSI, thrombosis, occlusion, and overall adverse events in hospitalized adult patients receiving select antibiotics and/or vasopressors through PICC or MC.

Methods

This retrospective chart review comprised patients admitted to intensive care units (ICU) at a quaternary medical center in Texas between April 2021 and September 2022. We included patients who received ciprofloxacin, levofloxacin, meropenem, vancomycin, dobutamine, dopamine, epinephrine, milrinone, norepinephrine, phenylephrine, and/or vasopressin through either a PICC or MC. Based on our hospital policy, these medications were allowed to be administered in either PICC or MC. Patients who received CVC or both PICC and MC during their stay were excluded.

We evaluated all positive blood cultures collected between 2 days after line insertion and up to 2 days after line removal. Two authors (BG and MA) reviewed charts to adjudicate whether the positive blood cultures were secondary to line infection (CRBSI), blood culture contamination, or an alternative infection source (eg, intraabdominal infection or pneumonia). Thrombosis was defined as either symptomatic deep vein thrombosis (DVT) or superficial venous thrombosis (SVT) in the ipsilateral arm to the catheter diagnosed 2 days after line insertion and up to 2 days after line removal. Occlusion was defined as the need for intra-catheter administration of alteplase (2 mg) for which an alternative indication was not documented. Device days were defined as days in which a line was in place and were not necessarily continuous. Days in which patients had multiple devices of one type inserted were counted as a single day.

The study outcomes included CRBSI, thrombosis (DVT or SVT), occlusion, and overall adverse events. Incidence rate comparison, 30-day Kaplan-Meier survival curves, and the log-rank test were used to compare incidence rate ratios (IRR) or hazard ratios (HR), as appropriate, between patients receiving MC and PICC. Day 0 was considered the date of line insertion, and patients who died within 30 days were censored. Multiple Cox proportional hazard regression models were employed to adjust for potential confounding factors, including age, gender, ICU type (medical vs surgical), and duration of antibiotics and vasopressors. An alpha level of 0.05 was used to determine statistical significance. The analysis was done using R version 4.2.2 (Vienna, Austria).

Results

A total of 445 patients were included, with 359 (80.7%) receiving select antibiotics and/or vasopressors via MC and 86 (19.3%) via PICC. There were 3,910 device days in the MC group, versus 987 in the PICC group. All lines had documented insertion and removal dates. The overall median device days were 9 (interquartile range [IQR] 5–14), with MC and PICC in place for a median of 8 (IQR 5–14) and 9 days (IQR 6–14), respectively. Patient characteristics were similar across the two device types in age, gender, race/ethnicity, and unit (medical vs surgical ICU). The median antibiotic and vasopressor days of therapy (DOT) were 3 (IQR 1–5) and 0 days (IQR 0–2) in the MC group compared to 3 (IQR 1–6; P = 0.549) and 0 (IQR 0–2; P = 0.1) in the PICC group, respectively.

The incident rate for CRBSI was 0.18 infections per device day (0.2 in the MC vs 0.1 in the PICC; IRR 2.02; 95% CI, 0.27, 89.61). The incident rate for thrombosis was 0.43 (0.49 in the MC vs 0.2 in the PICC; IRR 2.40; 95% CI, 0.58, 21.23). Regarding occlusion, the incidence rate was 0.29 (0.1 in the MC vs 1.01 in the PICC; IRR 0.1; 95% CI, 0.02, 0.35).

There were no differences in HR of CRBSI (Figure 1, P = 0.39), thrombosis (P = 0.24), or total events (P = 0.22) across the 2 study groups; however, the HR for occlusion was higher in the PICC compared with the MC (P < 0.001). The results were similar after adjusting for confounders (Table 1), as there was no difference in CRBSI (HR 0.35; P = 0.377), thrombosis (HR 0.40; P = 0.218), or total events (HR 1.49; P = 0.250) between the MC and PICC, while the occlusion was higher in the PICC group (HR 9.81; P < 0.001). Vasopressor DOT was independently associated with increased CRBSI (HR 1.16; P = 0.006) and total adverse events (HR 1.10; P = 0.005), while antibiotic DOT was associated with increased thrombosis (HR 1.07; P = 0.017).

Figure 1.

Kaplan-Meier survival curves comparing MC and PICC. This figure represents the survival rates for the 2 study groups: midline catheters (blue) and peripherally inserted central catheters (red). Four outcomes are shown: bloodstream infections (top left), thrombosis (DVT or SVT) (top right), occlusion (bottom left), and all events (bottom right). The log-rank P values are presented in each panel. MC, midline catheters; PICC, peripherally inserted central catheters; BSI, bloodstream infections; DVT, deep vein thrombosis; SVT, superficial vein thrombosis.

Table 1.

Cox proportional hazard multivariable models for study outcomes

Note. CRBSI, catheter-related bloodstream infections; DVT or SVT, deep vein thrombosis or superficial venous thrombosis; HR, hazard ratios; CI, confidence interval; PICC, peripherally inserted central catheters; MC, midline catheters; SICU, Surgical Intensive Care Unit; MICU, Medical Intensive Care Unit; DOT, days of therapy.

Discussion

Our review suggests no difference between MC and PICC in CRBSI, thrombosis, or total adverse events; however, occlusion was higher in the PICC group. This aligns with previous studies suggesting that MC and PICC carry comparable risk profiles. This supports the idea that the choice of line type for hospitalized patients requiring short-term therapy need not be limited to CVC or PICC, even in patients requiring certain vesicant antibiotics or vasopressors. Strengths of our study included the absence of crossover between patients with MC and PICC, excluding patients with CVC, and controlling for the medication type infused through each line.

Our findings differ from a recent meta-analysis (3) that suggested that MC may be superior to PICC when comparing infection risk. One potential explanation for the difference in results may lie in the vesicant nature of the medications selected. Indeed, vasopressor DOT were independently associated with a small yet significant increase in the risk of CRBSI and total adverse events, while antibiotic DOT were associated with a small risk for thrombosis. Importantly, this association was irrespective of device type, and our study did not have sufficient power to detect between-group differences.

Our study has several limitations. The occlusion of MC may have been under-identified as MC may have been replaced rather than salvaged with alteplase if found nonfunctioning We did not have information on the number of lumens in each device, which made it not possible to assess the role of the number of lumens on device outcomes. Blood cultures were manually reviewed non-blinded, leading to potential information bias. We have included several potential confounders in the multiple regression models (age, ICU type, DOT). Still, it is possible that there are differences in outcomes related to unmeasured confounders (eg, comorbidities). Our study was insufficiently powered to ascertain the true differences between MC and PICC. Finally, the findings are limited to one academic medical center, limiting generalizability.

Conclusion

Our study suggests no difference between CRBSI, thrombosis, or total adverse events rates in hospitalized patients receiving vesicant medications through either MC or PICC; however, the study was not powered enough to detect differences. Larger studies are needed to assess the safety of administering these medications via MC in hospitalized patients.

Acknowledgments

None.

Financial support

There was no funding for this project.

Competing interests

All authors have nothing to disclose.

References

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Figure 0

Figure 1. Kaplan-Meier survival curves comparing MC and PICC. This figure represents the survival rates for the 2 study groups: midline catheters (blue) and peripherally inserted central catheters (red). Four outcomes are shown: bloodstream infections (top left), thrombosis (DVT or SVT) (top right), occlusion (bottom left), and all events (bottom right). The log-rank P values are presented in each panel. MC, midline catheters; PICC, peripherally inserted central catheters; BSI, bloodstream infections; DVT, deep vein thrombosis; SVT, superficial vein thrombosis.

Figure 1

Table 1. Cox proportional hazard multivariable models for study outcomes