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1 inistered at the time of large-volume (>5 L) paracentesis.
2 Complications occurred in 5.7% of AC paracentesis.
3 al load at time of positive anterior chamber paracentesis.
4 1.3% female, mean age 56.7 years) and 528 AC paracentesis.
5 ated the safety and diagnostic utility of AC paracentesis.
6 ferior vena cava filter, gastric bypass, and paracentesis.
7 cedural hemorrhage among patients undergoing paracentesis.
8 nly 1 patient (SOC group) after large-volume paracentesis.
9 anterior chamber (AC) via peripheral corneal paracentesis.
10 ents undergoing therapeutic anterior chamber paracentesis.
11 vatively and 59 patients received additional paracentesis.
12 on systemic hemodynamics at patients' first paracentesis.
13 04), and 6 hours (+6 mmHg); p = 0.050) after paracentesis.
14 between first symptoms and implementation of paracentesis.
15 chylous effusions normally requires invasive paracentesis.
16 er current standard therapy with and without paracentesis.
17 r refractory ascites frequently necessitates paracentesis.
18 ), and 6 hours (6; IQR 4-6; p = 0.012) after paracentesis.
19 5/m2; p = 0.016) when measured 2 hours after paracentesis.
20 een first symptoms and the implementation of paracentesis.
21 because of PCR results from anterior chamber paracentesis.
22 and improves outcome following large volume paracentesis.
23 line and at key time points during and after paracentesis.
24 and (3) the resources used for large-volume paracentesis.
25 opriate when experienced personnel carry out paracentesis.
27 osis who underwent therapeutic thoracentesis/paracentesis, 177 met criteria for RH and 422 for RA.
28 ys was observed in 26.7% of patients without paracentesis, 36.4% of patients with paracentesis within
30 ntrolled, compared to patients with need for paracentesis 6 weeks after TIPS (median survival: 185 vs
31 50 patients with sterile ascites on initial paracentesis, 7 patients developed peritonitis during fo
33 ted in charts, were common for patients with paracentesis after diagnosis with ascites, patients that
34 alopathy, and long-term (>3 months) need for paracentesis after TIPS placement were evaluated and cal
35 rvey study to assess practice patterns on AC paracentesis and a retrospective diagnostic and safety s
36 al load at time of positive anterior chamber paracentesis and association between topical corticoster
37 atedly administered topically 3 hours before paracentesis and continued for 90 minutes afterward.
41 or chamber (AC) through a clear corneal 1 mm paracentesis and directed at the trabecular meshwork adj
43 ey injury (AKI) and death after large-volume paracentesis and in patients with spontaneous bacterial
44 he patient was treated with anterior chamber paracentesis and intraocular pressure lowering drops.
46 the absence of any tangible effectiveness of paracentesis and the inherent risks of paracentesis such
48 drothorax should be managed with therapeutic paracentesis and/or thoracentesis, respectively, with th
49 had a complete response (required no further paracentesis) and 11 patients (22%) had a partial respon
50 ast year of life (not involving large-volume paracentesis), and number of large-volume paracentesis p
52 omes were alteration of treatment, safety of paracentesis, and correlation of keratitic precipitates
53 ent; infectious workup, including diagnostic paracentesis, and evaluation of secondary causes (thyroi
54 es foci of sepsis, for appropriate sites for paracentesis, and to assess for vascular disorders such
55 herapy to ascites [repeated thoracentesis or paracentesis, and transjugular intrahepatic portosystemi
56 reated with ocular massage, anterior chamber paracentesis, and/or hemodilution (conservative treatmen
57 r placement; lumbar puncture; thoracentesis; paracentesis; and intubation/mechanical ventilation) was
59 r (50 mul) were obtained by anterior chamber paracentesis as the first step of routine cataract surge
61 s with tense ascites undergoing large-volume paracentesis, as compared with alternative treatments in
63 patients with cirrhosis who had their first paracentesis at the Medical University of Vienna from 20
64 ients who underwent at least 1 outpatient AC paracentesis at UCSF from 2012 to 2023 were included in
65 n infusion is recommended after large-volume paracentesis, at diagnosis of spontaneous bacterial peri
66 atients with (BCVA 1.9 +/- 0.31) and without paracentesis (BCVA 1.75 +/- 0.32) (p = 0.9), nor among t
69 d in conjunction with occurence rate of post-paracentesis clinically significant hemorrhage, defined
70 2 L of drainage and 94.3 pg/mL at the end of paracentesis, compared with an increase of 10.5 pg/mL an
72 s were to determine (1) whether large-volume paracentesis could be performed safely and effectively b
74 is such as intraocular infection and injury, paracentesis does not appear to be warranted as a treatm
77 s ascites should be treated with therapeutic paracentesis followed by colloid volume expansion, and d
79 with cirrhosis, patients undergoing lateral paracentesis had a mean MELD 3.0 score of 22 ( sd , 8.46
80 and were more likely to require therapeutic paracentesis (HR 2.26; p = 0.02) in the next 90 days.
81 peritonitis (HR, 0.55 [95% CI, 0.46-0.65]), paracentesis (HR, 0.54 [95% CI, 0.50-0.60]), variceal bl
84 and respiratory parameters before and after paracentesis in 50 critically ill patients with advanced
85 serious complication of large-volume (>5 L) paracentesis in cirrhosis and is reduced with albumin in
87 sfunction with increased odds of post-90-day paracentesis in outpatient TIPS, hospital admissions for
88 p reduces or abrogates the need for repeated paracentesis in patients with recurrent or refractory as
90 portosystemic shunts (TIPS) vis-a-vis total paracentesis in the management of refractory ascites is
92 added gain in visual acuity by performing a paracentesis, independent of the time elapsed between fi
96 ous humor liquid biopsy via anterior chamber paracentesis is a safe and well-tolerated procedure in p
98 c agents and hyaluronidase, anterior chamber paracentesis, IV corticosteroid, IV mannitol, and hyperb
100 anges in serum NT-proBNP during large volume paracentesis (LVP) in patients with ascites have never b
102 ithin 7-24 hours, and 23.1% of patients with paracentesis more than 24 hours after the onset of sympt
103 hether PICD could develop with modest-volume paracentesis (MVP) and the role of albumin infusion.
104 ( sd , 8.46) and patients undergoing midline paracentesis ( n = 118) had a mean MELD 3.0 score of 25
105 py (sodium restriction, diuretics, and total paracentesis) (n = 57) or medical therapy plus TIPS (n =
107 The potential association of low-volume paracentesis of less than 5 L with complications in pati
109 e ascites or requiring frequent large-volume paracentesis on conservative treatment are likely to req
110 our study was to investigate the effects of paracentesis on hemodynamic and respiratory parameters i
111 er disease and tense ascites who performed a paracentesis on himself and developed K. kingae peritoni
114 ascites is managed by repeated large volume paracentesis or insertion of a transjugular intrahepatic
115 neficial in patients undergoing large-volume paracentesis or who have hepatorenal syndrome or spontan
116 hy, ascites requiring sustained diuretics or paracentesis, or coagulopathy unresponsive to vitamin K
117 variceal bleeding, hepatocellular carcinoma, paracentesis, or hemodialysis; and discharge against med
118 oma medications, performing anterior chamber paracentesis, or increasing the interval between injecti
120 est and could forego the need for diagnostic paracentesis, particularly in cases where the cause of a
121 nostic and safety study of all outpatient AC paracentesis performed between April 2012 and March 2023
122 identify complications from anterior chamber paracentesis performed to obtain AH for liquid biopsy.
123 AO) such as ocular massage, anterior chamber paracentesis, physical exercise, and medication-induced
124 hthalmology residents each performed four AC paracentesis procedures (two with the novel device, two
126 tesis ratio (number of day-case large-volume paracentesis procedures as a proportion of the total num
127 rrelated with the proportion of large-volume paracentesis procedures done in a day-case (vs unplanned
130 day-case paracentesis service (care group), paracentesis ratio (number of day-case large-volume para
133 e or much more confident about performing AC paracentesis safely with the novel syringe handle than w
134 ife to death, whether enrolled in a day-case paracentesis service (care group), paracentesis ratio (n
135 atients who attended a day-case large-volume paracentesis service within their last year of life had
136 RPRETATION: The use of day-case large-volume paracentesis services in the last year of life was assoc
137 up showed better ascites control, with fewer paracentesis sessions per month (1.57 +/- 0.65 vs. 4.07
138 ent either liver biopsy of mass or abdominal paracentesis, showing gallbladder cancer and adenocarcin
139 mes included incidence of variceal bleeding, paracentesis, spontaneous bacterial peritonitis, hepatic
142 ss of paracentesis and the inherent risks of paracentesis such as intraocular infection and injury, p
143 hage at the procedural site within 7 days of paracentesis that required either blood transfusion, ang
144 vitreal antibiotics with an anterior chamber paracentesis that was not sent for microbiologic samplin
147 and coagulopathy before low-risk therapeutic paracentesis, thoracentesis, and routine upper endoscopy
148 who required more than one anterior chamber paracentesis to detect CMV as the etiologic agent of the
150 with medium-chain triglycerides, therapeutic paracentesis, total parenteral nutrition, and somatostat
151 mong those currently under investigation are paracentesis, ultrafiltration, peritoneal dialysis, oral
153 ed syringe handle that enables one-handed AC paracentesis using standard 1-mL syringes by allowing si
154 increase in handgrip strength, reduction in paracentesis volume, and improved quality of life in pat
161 xperimental chickens subjected to unilateral paracentesis were fixed either by perfusion or in situ,
162 and respiratory parameters before and after paracentesis were performed by Wilcoxon signed-rank test
163 A total of 80 ACLF patients undergoing <5 L paracentesis were randomized to receive albumin (8 g/dL
164 A total of 80 ACLF patients undergoing <5 L paracentesis were randomized to receive albumin (8-10 g/
165 ped a novel syringe handle for one-handed AC paracentesis, which improved the safety and precision of
166 dard of care (SOC; ie, repeated large-volume paracentesis with albumin infusion), and were hospitaliz
172 cornea and/or uveitis (68%) and performed AC paracentesis with the patient at the slit lamp (75%).
173 ta-analyses on trials comparing large-volume paracentesis with transjugular intrahepatic portosystemi
174 ne patient suffered a lens injury due to the paracentesis, with subsequent need for cataract surgery.
175 iotics within 48 hours, i.v. albumin, repeat paracentesis within 48 hours, recognition of SBP, and pr
176 without paracentesis, 36.4% of patients with paracentesis within 6 hours, 20% of patients with parace
177 entesis within 6 hours, 20% of patients with paracentesis within 7-24 hours, and 23.1% of patients wi