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Talc slurry versus thoracoscopic talc insufflation for malignant pleural effusion: a systematic review and meta-analysis
Rodrigues, Anna Luíza Soares de Oliveira; Souza, Maria Eduarda Cavalcanti; Moraes, Francisco Cezar Aquino de; Lima, David Paes de; Carvalho, Rafael Lucas Costa de.
Affiliation
  • Rodrigues, Anna Luíza Soares de Oliveira; Centro Universitário de João Pessoa. João Pessoa. BR
  • Souza, Maria Eduarda Cavalcanti; Universidade de Pernambuco. Recife. BR
  • Moraes, Francisco Cezar Aquino de; Universidade Federal do Pará. Belém. BR
  • Lima, David Paes de; Universidade de São Paulo. Instituto do Coração. Divisão de Cirurgia Torácica. São Paulo. BR
  • Carvalho, Rafael Lucas Costa de; Universidade de São Paulo. Instituto do Coração. Divisão de Cirurgia Torácica. São Paulo. BR
J. bras. pneumol ; J. bras. pneumol;50(3): e20240115, 2024. tab, graf
Article in En | LILACS-Express | LILACS | ID: biblio-1569306
Responsible library: BR1.1
ABSTRACT
ABSTRACT

Objective:

Talc pleurodesis is a widely used treatment option for malignant pleural effusion (MPE). However, the optimal form of administration remains controversial. Thus, we performed a systematic review and meta-analysis to assess the effectiveness of talc slurry (TS) in comparison with thoracoscopic talc insufflation/poudrage (TTI) for MPE treatment.

Methods:

We searched PubMed, EMBASE, and Cochrane Library databases for studies that compared TS with TTI in patients with MPE. We used a random-effects model with a 95% CI to pool the data. Heterogeneity was assessed with I2 statistics.

Results:

We included eight studies involving 1,163 patients, 584 of whom (50.21%) underwent TS. Pleurodesis failure rates were similar between the procedures (OR = 1.07; 95% CI 0.56-2.06; p = 0.83; I2 = 62%); and 68% of patients (95% CI 0.31-1.47; p = 0.33; I2 = 58%) had postoperative complications, which were lower in patients in the TS group than in the TTI group. In a subgroup analysis considering only randomized clinical trials, the failure rate was significantly lower in the TS treatment group (OR = 0.62; 95% CI 0.42-0.90; p = 0.01; I2 = 0%). Similarly, dyspnea was less common in the TS group (OR = 0.74; 95% CI 0.41-1.34; p = 0.32; I2 = 55%). Adverse effects were reported in 86 patients, and no significant difference was seen between the TS and TTI groups empyema (OR = 1.43; 95% CI 0.36-5.64; p = 0.86; I2 = 0%), pain (OR = 1.22 (95% CI 0.67-2.21; p = 0.51; I2 = 38%), and pneumonia (OR = 1.15; 95% CI 0.30-4.46; p = 0.86; I2 = 27%).

Conclusions:

Our findings suggest that TS is an effective treatment for MPE, with no significant increase in adverse events. Results suggest equivalent efficacy and safety for both procedures.
Key words

Full text: 1 Collection: 01-internacional Database: LILACS Language: En Journal: J. bras. pneumol Journal subject: PNEUMOLOGIA Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: Brazil

Full text: 1 Collection: 01-internacional Database: LILACS Language: En Journal: J. bras. pneumol Journal subject: PNEUMOLOGIA Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: Brazil