FDA Adverse Event Injury Summary report: N

SINGLE USE ASPIRATION NEEDLE NA-U200H

MDR report key: 16207921 · Received January 19, 2023

Report

Report Number
2429304-2023-00009
Event Type
Injury
Date Received
January 19, 2023
Date of Event
March 12, 2022
Report Date
January 19, 2023
Manufacturer
OLYMPUS AMERICA, INC
Product Code
FCG
UDI-DI
04953170380440
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Description of Event or Problem · 0

OLYMPUS MEDICAL SYSTEMS CORP. (OMSC) RECEIVED A LITERATURE TITLED, "ENDOSCOPIC ULTRASOUND-GUIDED PORTO-SYSTEMIC PRESSURE GRADIENT MEASUREMENT CORRELATES WITH HISTOLOGICAL HEPATIC FIBROSIS". BACKGROUND AND AIMS ENDOSCOPIC ULTRASOUND IS A NOVEL DIAGNOSTIC APPROACH TO CHRONIC LIVER DISEASES (CLDS), AND EUS-GUIDED PORTO-SYSTEMIC PRESSURE GRADIENT MEASUREMENT (EUS-PPG) IS AN IMPORTANT EXPANSION WITH A WELL-DEVELOPED TECHNIQUE. HOWEVER, THE CLINICAL VALUE AND APPLICABILITY OF EUS-PPG MEASUREMENT IN PREDICTING HISTOLOGICALLY ADVANCED HEPATIC FIBROSIS REMAIN UNKNOWN. METHODS THIS WAS A SINGLE-CENTER RETROSPECTIVE STUDY ON PATIENTS WITH VARIOUS CLDS UNDERGOING EUS-PPG AND EUS-GUIDED LIVER BIOPSY (EUS-BX) TO ASSESS IF EUS-PPG MEASUREMENTS CORRELATE WITH HISTOLOGICAL FIBROSIS STAGE AND VARIOUS SURROGATE MARKERS FOR SEVERITY OF CLDS AND ITS SAFETY. CASES WITH EUS-PPG WERE IDENTIFIED AT THE UNIVERSITY OF CALIFORNIA IRVINE, A TERTIARY ENDOSCOPY CENTER, BETWEEN JANUARY 2014 AND MARCH 2020. RESULTS IN 64 PATIENTS, THE MEAN AGE WAS 57.5; 40 (62.5%), MALES; MEAN CHILD-TURCOTTE-PUGH (CTP) AND MODEL FOR END-STAGE LIVER DISEASE (MELD) SCORES, 5.9 AND 10.4, RESPECTIVELY. THE PROCEDURE SUCCESS RATE WAS 100%. TWENTY-NINE (45.3%) HAD EUS-PPG¿=¿5 MMHG THAT WAS ASSOCIATED WITH CLINICAL CIRRHOSIS (P¿<¿0.0001), CLINICAL PORTAL HYPERTENSION (P¿=¿0.002), HEPATIC DECOMPENSATION (P¿=¿0.013), MELD-NA¿>¿10 (P¿=¿0.036), PLTS¿=¿120¿×¿109/L (P¿=¿0.001), INR¿=¿1.05 (P¿=¿0.007), PRESENCE OF EV, GV, OR PHG (P¿<¿0.0001), BIOPSY-PROVEN FIBROSIS STAGE¿=¿3 (P¿=¿0.002), APRI¿>¿2 (P¿=¿0.001), AND FIB-4¿>¿3.25 (P¿=¿0.001). MULTIVARIABLE ANALYSIS CONFIRMED THAT EUS-PPG¿=¿5 MMHG WAS SIGNIFICANTLY ASSOCIATED WITH LIVER BIOPSY-PROVEN FIBROSIS STAGE¿=¿3 (LR 27.0, 95% CI¿=¿1.653¿360.597, P¿=¿0.004), INDEPENDENT OF C-CIRRHOSIS, C-PHTN, THROMBOCYTOPENIA, SPLENOMEGALY, AND APRI SCORE¿>¿2, AND FIB-4 SCORE¿>¿3.25. THERE WERE NO SERIOUS COMPLICATIONS RELATED TO EUS-PPG PROCEDURES. CONCLUSIONS EUS-PPG MEASUREMENTS PROVIDE EXCELLENT CORRELATION WITH HISTOLOGICAL HEPATIC FIBROSIS STAGE AND VARIOUS CLINICAL, LABORATORY, ENDOSCOPIC AND IMAGING VARIABLES INDICATIVE OF ADVANCED LIVER DISEASE WITHOUT SERIOUS ADVERSE EVENTS. TYPE OF ADVERSE EVENTS/NUMBER OF PATIENTS CIRRHOSIS THROMBOCYTOPENIA. THIS LITERATURE ARTICLE REQUIRES 3 REPORTS. THE RELATED PATIENT IDENTIFIERS ARE AS FOLLOWS: 1. (B)(6). 2. (B)(6). 3. (B)(6). THIS MEDWATCH REPORT IS FOR PATIENT IDENTIFIER (B)(6). THERE IS NO REPORT OF ANY OLYMPUS DEVICE MALFUNCTION IN ANY PROCEDURE DESCRIBED IN THIS STUDY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
405711 SINGLE USE ASPIRATION NEEDLE NA-U200H SINGLE USE ASPIRATION NEEDLE FCG OLYMPUS AMERICA, INC NA-U200H-8019S UNKNOWN (LITERATURE) 04953170380440

Patients

Seq Age Sex Outcome Treatment
1 Unknown Other